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Executive Director, Medical Affairs, Genitourinary at Merck Sharp & Dohme Corp. /Netherlands
North Wales, Pennsylvania, United States - Full Time
Skills Needed
Budget Management, Clinical Development, Executive Leadership, Genitourinary, Global Experience, Medical Affairs, Medical Oncology, Oncology, People Leadership, Professional Integrity, Professional Networking, Scientific Exchange, Scientific Leadership, Strategy Development
Specialization
Candidates must have extensive experience in medical affairs or clinical development, with a strong track record of team leadership and global experience. An M.D., Ph.D., DDS/DMD, or Pharm.D. is required, with a preference for an M.D.
Experience Required
Minimum 10 year(s)
Dean of Academic Affairs - Nursing- Irving Campus at Adtalem Global Education
Irving, Texas, United States - Full Time
Skills Needed
Leadership, Nursing Education, Curriculum Development, Student Success, Faculty Engagement, Communication, Organizational Skills, Conflict Resolution, Mentoring, Compliance, Budget Management, Team Collaboration, Program Development, Quality Improvement, Time Management, Professionalism
Specialization
Candidates must have a Master's Degree in nursing, with a Doctorate preferred, and at least 5 years of full-time experience in nursing education, including 3 years in a leadership role. Strong interpersonal, organizational, and communication skills are essential.
Experience Required
Minimum 5 year(s)
Global Medical Affairs Oncology Governance Intern at DAIICHI SANKYO INC
Basking Ridge, New Jersey, United States - Full Time
Skills Needed
Fda Regulations, Ich Regulations, Health Authority Regulations, Compliance, Writing Processes, Clinical Trial Development, Clinical Trial Operations, Investigation, Root Cause Analysis, Document Review, Sop Review, Capa Planning, Action Resolution, Summary Findings, Protocol Review, Gaps Identification
Specialization
Candidates should have a basic understanding of FDA and ICH regulations and an interest in health authority regulations and compliance. Knowledge about writing processes and clinical trial development is also required.
Dean of Academic Affairs - Nursing- Irving Campus at Adtalem Global Education
Irving, Texas, United States - Full Time
Skills Needed
Leadership, Nursing Education, Curriculum Development, Student Success, Faculty Management, Compliance, Conflict Resolution, Communication, Organizational Skills, Mentoring, Budget Management, Program Development, Team Collaboration, Quality Improvement, Time Management, Professionalism
Specialization
A Master's Degree in nursing is required, with a Doctorate preferred, along with 5+ years of nursing education experience and at least 3 years in a leadership role. Strong interpersonal and organizational skills, as well as current RN licensure in Texas, are also necessary.
Experience Required
Minimum 5 year(s)
Senior Director of US Government Affairs (Remote) at Jobgether
, , United States - Full Time
Skills Needed
Federal Government Affairs, Lobbying, Policy Analysis, Stakeholder Engagement, Manufacturing Policy, Trade Regulations, Electronic Materials, Interpersonal Skills, Communication Skills, Judgment, Integrity, Discretion, Collaboration, Strategic Advocacy, Legislative Environment, Regulatory Environment
Specialization
Candidates must have a minimum of 7 years of experience in federal government affairs, ideally with a focus on manufacturing, healthcare, and trade issues. Strong interpersonal and communication skills, along with a proven track record in lobbying, are essential.
Experience Required
Minimum 10 year(s)
Executive Director, Head of Japan Medical Affairs at Revolution Medicines
, , Japan - Full Time
Skills Needed
Oncology, Medical Affairs, Leadership, Collaboration, Clinical Trials, Regulatory Compliance, Stakeholder Engagement, Strategic Planning, Budget Management, Communication, Team Development, Data Interpretation, Market Access, Kol Engagement, Scientific Communication, Pharmacovigilance, Real World Evidence
Specialization
An advanced scientific degree (MD, PhD, or PharmD) with significant experience in oncology is required, along with a minimum of 10 years in Medical Affairs. Proven leadership skills and a strong understanding of the Japan oncology landscape are essential.
Experience Required
Minimum 10 year(s)
Affiliate Head of Quality and Regulatory Affairs at F. Hoffmann-La Roche Ltd - Poland
Hod HaSharon, Center District, Israel - Full Time
Skills Needed
Quality Management, Regulatory Affairs, Iso 9001:2015, Auditing, Gmp, Gdp, Ivdr, Mdr, Capa, Training, Stakeholder Engagement, Process Improvement, Leadership, Communication, Life Sciences, Diagnostics, Healthcare
Specialization
Candidates should have a BA/BS, MS, or PhD in Life Sciences, Medical, or Engineering fields with 5-10 years of experience in a Quality-regulation related role. Expertise in ISO standards and familiarity with healthcare systems in Israel is essential.
Experience Required
Minimum 5 year(s)
Senior Manager, Business & Legal Affairs, Sports at Netflix
Los Angeles, California, United States - Full Time
Skills Needed
Business Affairs, Legal Affairs, Live Sports Production, Negotiation, Contract Drafting, Communication, Leadership, Analytical Skills, Time Management, Strategic Thinking, Problem Solving, Collaboration, Production Counsel, Licensing, Guilds And Unions Knowledge, Music Rights
Specialization
Candidates should have at least eight years of experience in business and legal affairs related to live sports and events. A J.D. and membership in good standing in a state bar are required, along with strong leadership and communication skills.
Experience Required
Minimum 10 year(s)
Director, Government Business & Government Affairs at Boston Scientific Corporation Malaysia
Gurugram, haryana, India - Full Time
Skills Needed
Policy Development, External Relations, Government Affairs, Public Private Partnerships, Pricing Strategies, Stakeholder Engagement, Health Economics, Reimbursement Strategies, Competitor Analysis, Public Affairs, Team Leadership, Collaboration, Functional Excellence, Insights Generation, Project Management, Tender Participation
Specialization
The role requires building relationships with key decision-makers and providing insights into upcoming policies and regulations. It also involves leading teams and ensuring technical readiness for tenders.
Experience Required
Minimum 10 year(s)
Senior Regulatory Affairs Specialist - Endoscopy at Boston Scientific Corporation Malaysia
Georgetown, Massachusetts, United States - Full Time
Skills Needed
Regulatory Affairs, Medical Devices, Fda Regulations, Eu Mdr, International Regulations, Product Development, Design Control, Clinical Trials, Project Management, 510(k), Pma, Ide, Technical Writing, Microsoft Office, Communication Skills, Editing Skills
Specialization
A Bachelor's degree or equivalent work experience is required, preferably in a scientific or technical discipline. Candidates should have a minimum of 4 years' experience in Regulatory Affairs within the medical device industry.
Experience Required
Minimum 5 year(s)
Sr. Director, Regulatory Affairs (Tarrytown, NY) at Global Financial Impact - Edwin Alvarado
Tarrytown, New York, United States - Full Time
Skills Needed
Regulatory Compliance, Product Development, Labeling Compliance, Nda Submissions, Medical Devices, Otc Drugs, Cosmetics Regulations, Dietary Supplements, Team Management, Communication Skills, Quality Assurance, Risk Assessment, Global Regulatory Monitoring, Sop Development, Industry Knowledge, Audits
Specialization
Candidates must have a Bachelor's degree in a scientific or health-related field, with a Master's degree preferred. A minimum of 15 years of experience in pharmaceutical or medical device regulatory affairs is required.
Experience Required
Minimum 10 year(s)
Affiliate Head of Quality and Regulatory Affairs at F. Hoffmann-La Roche Ltd - Poland
Hod HaSharon, Center District, Israel - Full Time
Skills Needed
Quality Management, Regulatory Affairs, Iso 9001:2015, Auditing, Gmp, Gdp, Ivdr, Mdr, Capa, Training, Stakeholder Engagement, Process Improvement, Leadership, Communication, Life Sciences, Diagnostics, Healthcare
Specialization
Candidates should have a BA/BS, MS, or PhD in Life Sciences, Medical, or Engineering fields with 5-10 years of relevant experience. Expertise in ISO standards and a strong understanding of healthcare systems in Israel are essential.
Experience Required
Minimum 5 year(s)
Executive Manager, Government & Industry Affairs at Commonwealth Bank
Sydney, New South Wales, Australia - Full Time
Skills Needed
Policy Campaigning, Advocacy, Public Policy Development, Analytical Skills, Communication Skills, Relationship Management, Interpersonal Skills, Judgement, Discretion, Professionalism, Team Culture, Risk Management, Research, Monitoring, Political Analysis, Regulatory Analysis
Specialization
Candidates should have expertise in policy campaigning and advocacy, with strong analytical and communication skills. Experience in government, banking, finance, or a related field is highly regarded.
Experience Required
Minimum 5 year(s)
Nevada Gold Mines - Community Affairs Specialist at Barrick
, , - Full Time
Skills Needed
Community Engagement, Public Relations, Communication Skills, Team Player, Crisis Management, Stakeholder Engagement, Organizational Skills, Education Programs, Mining Industry Knowledge, Environmental Regulations, Computer Proficiency, Independent Work, Multi Tasking, Matrix Structure Support
Specialization
Candidates must have a bachelor's degree in a relevant field and three years of experience in community relations or six years of applicable experience. Strong communication skills and the ability to work independently and as part of a team are essential.
Experience Required
Minimum 2 year(s)
ELECTRIC/ELECTRONIC REGULATORY AFFAIRS TECHNICIAN at Eurofins
Barcelona, Catalonia, Spain - Full Time
Skills Needed
Regulatory Compliance, Electrical Products, Electronic Products, Bazaar Products, Toy Regulations, Technical Documentation, Regulatory Monitoring, Cen Cenelec Standards, Electrical Safety, Legal Framework Analysis, Consulting, Microsoft Excel, Organization, Methodical Work, Teamwork
Specialization
Candidates must have a higher vocational degree specializing in electrical/electronics, along with knowledge of the European and national regulatory-legal framework for the electrical/electronic sector and electrical safety in consumer products. A minimum of 2 years of experience, native Spanish, and medium-high level English are required.
Experience Required
Minimum 2 year(s)
Government Affairs and Community Relations Manager at Brightspeed
Columbus, Ohio, United States - Full Time
Skills Needed
Government Affairs, Community Relations, Stakeholder Engagement, Permitting, Regulatory Compliance, Public Policy, Advocacy, Cross Functional Coordination, Relationship Building, Communication, Problem Solving, Organizational Skills, Analytical Skills, Microsoft Office Proficiency, Telecommunications Knowledge, Broadband Deployment
Specialization
Candidates must have a Bachelor's degree in a related field or equivalent experience, along with a minimum of three years in government affairs, public policy, or community relations. Essential qualifications include being based in the Columbus, OH area and possessing strong knowledge of state/local government processes and excellent relationship-building skills.
Experience Required
Minimum 2 year(s)
Director of Regulatory Affairs & Quality Control at SINTX
Salt Lake City, Utah, United States - Full Time
Skills Needed
Regulatory Affairs, Quality Control, Fda Submissions, Risk Management, Quality Management System, Additive Manufacturing, Biomaterials, Lean Six Sigma, Clinical Collaboration, Product Launch, Lifecycle Management, Cross Functional Leadership, Strategic Planning, Supplier Audits, Post Market Surveillance, Compliance
Specialization
Candidates must have a bachelor's degree in a relevant field and at least 10 years of experience in regulatory affairs and quality within medical devices or biomaterials. Direct experience with FDA submissions and strong knowledge of quality standards is essential.
Experience Required
Minimum 10 year(s)
H&M Department Manager- Dayton Mall at H&M Group
Dayton, Ohio, United States - Full Time
Skills Needed
Leadership, Team Management, Sales Analysis, Profit Optimization, Customer Experience, Visual Merchandising, Recruitment, Performance Management, Fashion Awareness, Trend Analysis, Cost Efficiency, Scheduling, Operational Routines, Stock Management, Team Collaboration, Communication
Specialization
Successful candidates must be strong, ambitious leaders who enjoy taking responsibility, possess effective communication skills, and are analytical solution finders capable of managing statistics and numbers. The role requires being achievement-oriented, motivated by performance, and truly customer-centric.
Experience Required
Minimum 2 year(s)
Packing Clipping Department Worker 3 at KCARC
Vincennes, Indiana, United States - Full Time
Skills Needed
Attention To Detail, Quality Control, Teamwork, Multitasking, Time Management, Safety Compliance, Communication, Problem Solving
Specialization
Candidates should have the ability to maintain a flexible schedule and establish working relationships. Prior manufacturing experience and knowledge of a sewing facility are helpful but not required.
Bakery Department Clerk - Full Time at Ridley’s Family Markets
Rupert, Idaho, United States - Full Time
Skills Needed
Customer Relations, Communication, Product Knowledge, Pricing, Merchandising, Quality Control, Teamwork, Training, Sales, Display Management, Order Management, Suggestive Selling, Cost Control, Behavioral Skills, Bakery Products, Attention To Detail
Specialization
Candidates should possess knowledge of bakery items and be capable of pricing and merchandising products. Strong communication skills and the ability to work collaboratively are essential.
Executive Director, Medical Affairs, Genitourinary at Merck Sharp & Dohme Corp. /Netherlands
North Wales, Pennsylvania, United States -
Full Time

Start Date

Immediate

Expiry Date

24 Apr, 26

Salary

402700.0

Posted On

24 Jan, 26

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Yes

Skills

Budget Management, Clinical Development, Executive Leadership, Genitourinary, Global Experience, Medical Affairs, Medical Oncology, Oncology, People Leadership, Professional Integrity, Professional Networking, Scientific Exchange, Scientific Leadership, Strategy Development

Industry

Pharmaceutical Manufacturing

Description
Job Description The Executive Director, Value & Implementation Global Medical & Scientific Affairs (V&I GMSA), Global Therapeutic Area (TA), position resides in the V&I organization, which includes GMSA as well as Outcomes Research. This position, referred to as TA EDMA, is accountable for the alignment and execution of the GMSA portion of the Global V&I Plans for their assigned TAs that is disease specific and can at times involve asset components. The TA EDMA will allocate 50% of their strategic focus to support the United States (U.S.) and the remaining 50% supporting the rest of world. The TA EDMA may also be appointed as a V&I Lead for their disease/asset area(s), which includes additional organizationally aligned responsibilities. The TA EDMA fosters relationships and engages with global scientific leaders and key decision-makers to inform the V&I priorities. The TA EDMA brings subject-matter expertise along with a global view to the role that affords them to strategically partner with internal stakeholders around Global V&I priorities. This position is also a team leader who effectively manages and inspires a diverse team to achieve high performance and deliver exceptional results. The TA EDMA exemplifies our company’s leadership skills—namely, acting as a change catalyst, taking ownership and accountability, and displaying emotional intelligence—and sets these standards for their team. Primary Responsibilities: Accountable for the generation of the global strategic V&I plan, its global and regional execution, and facilitating the rollout to the countries. The V&I strategy guides the bidirectional, tactical execution of the V&I GMSA portion in partnership with Outcomes Research to guide real-world data generation. Aligns with Big Country Markets. Ensures robust two-way communication with U.S., China, and Japan Executive Directors (Eds) or equivalents. Captures market-specific needs and insights to inform global strategy, while also guiding local execution in alignment with global V&I plans. Integrates into the EDMA Tandem model to foster strategic clarity and executional excellence. Demonstrates enterprise leadership across geographies. Dedicates 50% of their strategic focus to the U.S., acting as a change catalyst—leading global planning while ensuring seamless integration with U.S. execution. Partners with U.S. EDMA and Health Systems EDs to align payor strategies, precision-medicine initiatives, and congress deliverables. Partners with the appropriate Product Development Team (PDT) and/or Asset Development Team (ADT), Global Brand, and V&I Outcomes Research leads to define clinical-development plans and brand strategies for assigned TAs. Ensures team contributes as relevant members to the PDT and/or ADT sub-teams (V&I, Value Evidence, Clinical, Commercial, Publications, and Label teams). Integrates end-to-end knowledge gaps across countries and regions to better inform the GMSA portion of our Global V&I plans, enabling the countries and regions to successfully implement their country or regional priorities. Applies expertise in country’s medical systems and clinical practice standards to guide Global Directors Medical Affairs (GDMAs) and/or Regional Directors Medical Affairs (RDMAs) and partners with Regional Strategy Leads (RSLs) to anticipate challenges, identify solutions, and implement actions that support adoption of new innovations. Monitors external clinical trends and scientific developments through systematic insight collection from group input meetings (GIMs), congresses, and other platforms to maintain up-to-date knowledge of emerging science, medicines, and vaccines. Demonstrates business acumen by guiding the team to ask insightful, elevated questions and challenge the status quo. Leverages assessments to integrate actionable medical insights from various countries and regions, informing both current and future needs of the global strategy, ultimately ensuring insights are implemented into actions and goals. Leads the team in engagement with international scientific leaders and other key stakeholders (therapeutic guideline committees, payers, public groups, government officials, medical societies) about our company’s emerging science. Ensures all scientific exchange for their TA(s) is aligned with a single global scientific-communications platform. Collaborates across V&I, including U.S. EDMAs, Regional Leaders, and Outcomes Research, embedding fully within PDT/ADT frameworks to provide subject-matter expertise, drive accountability, and enhance value through effective partnerships. Collaborates with Global Human Health (commercial) leaders to inform of the GMSA portion of V&I plans to ensure alignment, while independently leading the execution of these plans. Organizes regular management reviews to assess team’s activities and progress. Supports key countries with the development of local data-generation study concepts and protocols when requested. Understands and supports the Investigator-Initiated Study program in collaboration with the Executive Director Scientific Affairs (EDSA). Leads and develops a high-performing team focused on executional excellence, fostering a collaborative environment that supports professional growth and continuous improvement. Implements talent-management and development plans, proactively addressing challenges to enhance team. Demonstrates and champions our company’s Ways of Working, emphasizing innovation, medical modernization, defining team priorities, and focusing on the impact to the patient. Manages assigned budget with strong financial stewardship, ensuring delivery within a 3% variance. Responsible and accountable for making informed decisions when budgets change throughout the year. Education: M.D., Ph.D., DDS/DMD or Pharm.D. (M.D. strongly preferred) and recognized medical expertise. TA specialization as required and recognized scientific expertise. Required Experience and Skills: Extensive experience in medical affairs or clinical development. Track record of successful team leadership and global experience. Strong prioritization and decision-making skills with the ability to understand how decisions fit into the broader context of corporate strategies. Demonstrated ability to motivate, mentor, manage and provide clear, unambiguous expectations and priorities for the teams. Ability to effectively collaborate with and influence partners across divisions in a matrix environment. Excellent interpersonal, analytical, and communication skills (written and oral) in addition to results-oriented project-management skills. Preferred Experience and Skills: At least five years of global or U.S. medical affairs or clinical development experience with proven track record of contribution to medical or clinical-development strategies. Five years of leadership in the pharmaceutical industry, with teams having responsibility for scientific exchange and research support, preferably in relevant TA. Demonstrated successful leadership of strategic initiatives as evidenced by a successful track record of design/creation of and accountability for implementation of strategic solutions for critical aspects of medical affairs goals and objectives. Track record of successful team leadership and global experience. Customer expertise, especially of scientific leadership and other key stakeholders (payers, public groups, government officials, medical professional organizations), in the assigned therapeutic area. Proven ability to effectively influence company life-cycle management and data generation. Understanding of resourcing and budgeting. Required Skills: Budget Management, Clinical Development, Executive Leadership, Genitourinary, Global Experience, Medical Affairs, Medical Oncology, Oncology, People Leadership, Professional Integrity, Professional Networking, Scientific Exchange, Scientific Leadership, Strategy Development Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement​ We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts U.S. Hybrid Work Model Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as “remote”. The salary range for this role is $255,800.00 - $402,700.00 This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits. You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting. San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Regular Relocation: Domestic/International VISA Sponsorship: Yes Travel Requirements: 25% Flexible Work Arrangements: Hybrid Shift: Not Indicated Valid Driving License: No Hazardous Material(s): n/a Job Posting End Date: 02/13/2026 *A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID:R382830

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Responsibilities
The Executive Director is accountable for generating and executing the global strategic V&I plan, ensuring alignment with regional needs and facilitating rollout to countries. They lead a diverse team, fostering high performance and collaboration to achieve exceptional results.
Executive Director, Medical Affairs, Genitourinary at Merck Sharp & Dohme Corp. /Netherlands
North Wales, Pennsylvania, United States - Full Time
Skills Needed
Budget Management, Clinical Development, Executive Leadership, Genitourinary, Global Experience, Medical Affairs, Medical Oncology, Oncology, People Leadership, Professional Integrity, Professional Networking, Scientific Exchange, Scientific Leadership, Strategy Development
Specialization
Candidates must have extensive experience in medical affairs or clinical development, with a strong track record of team leadership and global experience. An M.D., Ph.D., DDS/DMD, or Pharm.D. is required, with a preference for an M.D.
Experience Required
Minimum 10 year(s)
Dean of Academic Affairs - Nursing- Irving Campus at Adtalem Global Education
Irving, Texas, United States - Full Time
Skills Needed
Leadership, Nursing Education, Curriculum Development, Student Success, Faculty Engagement, Communication, Organizational Skills, Conflict Resolution, Mentoring, Compliance, Budget Management, Team Collaboration, Program Development, Quality Improvement, Time Management, Professionalism
Specialization
Candidates must have a Master's Degree in nursing, with a Doctorate preferred, and at least 5 years of full-time experience in nursing education, including 3 years in a leadership role. Strong interpersonal, organizational, and communication skills are essential.
Experience Required
Minimum 5 year(s)
Global Medical Affairs Oncology Governance Intern at DAIICHI SANKYO INC
Basking Ridge, New Jersey, United States - Full Time
Skills Needed
Fda Regulations, Ich Regulations, Health Authority Regulations, Compliance, Writing Processes, Clinical Trial Development, Clinical Trial Operations, Investigation, Root Cause Analysis, Document Review, Sop Review, Capa Planning, Action Resolution, Summary Findings, Protocol Review, Gaps Identification
Specialization
Candidates should have a basic understanding of FDA and ICH regulations and an interest in health authority regulations and compliance. Knowledge about writing processes and clinical trial development is also required.
Dean of Academic Affairs - Nursing- Irving Campus at Adtalem Global Education
Irving, Texas, United States - Full Time
Skills Needed
Leadership, Nursing Education, Curriculum Development, Student Success, Faculty Management, Compliance, Conflict Resolution, Communication, Organizational Skills, Mentoring, Budget Management, Program Development, Team Collaboration, Quality Improvement, Time Management, Professionalism
Specialization
A Master's Degree in nursing is required, with a Doctorate preferred, along with 5+ years of nursing education experience and at least 3 years in a leadership role. Strong interpersonal and organizational skills, as well as current RN licensure in Texas, are also necessary.
Experience Required
Minimum 5 year(s)
Senior Director of US Government Affairs (Remote) at Jobgether
, , United States - Full Time
Skills Needed
Federal Government Affairs, Lobbying, Policy Analysis, Stakeholder Engagement, Manufacturing Policy, Trade Regulations, Electronic Materials, Interpersonal Skills, Communication Skills, Judgment, Integrity, Discretion, Collaboration, Strategic Advocacy, Legislative Environment, Regulatory Environment
Specialization
Candidates must have a minimum of 7 years of experience in federal government affairs, ideally with a focus on manufacturing, healthcare, and trade issues. Strong interpersonal and communication skills, along with a proven track record in lobbying, are essential.
Experience Required
Minimum 10 year(s)
Executive Director, Head of Japan Medical Affairs at Revolution Medicines
, , Japan - Full Time
Skills Needed
Oncology, Medical Affairs, Leadership, Collaboration, Clinical Trials, Regulatory Compliance, Stakeholder Engagement, Strategic Planning, Budget Management, Communication, Team Development, Data Interpretation, Market Access, Kol Engagement, Scientific Communication, Pharmacovigilance, Real World Evidence
Specialization
An advanced scientific degree (MD, PhD, or PharmD) with significant experience in oncology is required, along with a minimum of 10 years in Medical Affairs. Proven leadership skills and a strong understanding of the Japan oncology landscape are essential.
Experience Required
Minimum 10 year(s)
Affiliate Head of Quality and Regulatory Affairs at F. Hoffmann-La Roche Ltd - Poland
Hod HaSharon, Center District, Israel - Full Time
Skills Needed
Quality Management, Regulatory Affairs, Iso 9001:2015, Auditing, Gmp, Gdp, Ivdr, Mdr, Capa, Training, Stakeholder Engagement, Process Improvement, Leadership, Communication, Life Sciences, Diagnostics, Healthcare
Specialization
Candidates should have a BA/BS, MS, or PhD in Life Sciences, Medical, or Engineering fields with 5-10 years of experience in a Quality-regulation related role. Expertise in ISO standards and familiarity with healthcare systems in Israel is essential.
Experience Required
Minimum 5 year(s)
Senior Manager, Business & Legal Affairs, Sports at Netflix
Los Angeles, California, United States - Full Time
Skills Needed
Business Affairs, Legal Affairs, Live Sports Production, Negotiation, Contract Drafting, Communication, Leadership, Analytical Skills, Time Management, Strategic Thinking, Problem Solving, Collaboration, Production Counsel, Licensing, Guilds And Unions Knowledge, Music Rights
Specialization
Candidates should have at least eight years of experience in business and legal affairs related to live sports and events. A J.D. and membership in good standing in a state bar are required, along with strong leadership and communication skills.
Experience Required
Minimum 10 year(s)
Director, Government Business & Government Affairs at Boston Scientific Corporation Malaysia
Gurugram, haryana, India - Full Time
Skills Needed
Policy Development, External Relations, Government Affairs, Public Private Partnerships, Pricing Strategies, Stakeholder Engagement, Health Economics, Reimbursement Strategies, Competitor Analysis, Public Affairs, Team Leadership, Collaboration, Functional Excellence, Insights Generation, Project Management, Tender Participation
Specialization
The role requires building relationships with key decision-makers and providing insights into upcoming policies and regulations. It also involves leading teams and ensuring technical readiness for tenders.
Experience Required
Minimum 10 year(s)
Senior Regulatory Affairs Specialist - Endoscopy at Boston Scientific Corporation Malaysia
Georgetown, Massachusetts, United States - Full Time
Skills Needed
Regulatory Affairs, Medical Devices, Fda Regulations, Eu Mdr, International Regulations, Product Development, Design Control, Clinical Trials, Project Management, 510(k), Pma, Ide, Technical Writing, Microsoft Office, Communication Skills, Editing Skills
Specialization
A Bachelor's degree or equivalent work experience is required, preferably in a scientific or technical discipline. Candidates should have a minimum of 4 years' experience in Regulatory Affairs within the medical device industry.
Experience Required
Minimum 5 year(s)
Sr. Director, Regulatory Affairs (Tarrytown, NY) at Global Financial Impact - Edwin Alvarado
Tarrytown, New York, United States - Full Time
Skills Needed
Regulatory Compliance, Product Development, Labeling Compliance, Nda Submissions, Medical Devices, Otc Drugs, Cosmetics Regulations, Dietary Supplements, Team Management, Communication Skills, Quality Assurance, Risk Assessment, Global Regulatory Monitoring, Sop Development, Industry Knowledge, Audits
Specialization
Candidates must have a Bachelor's degree in a scientific or health-related field, with a Master's degree preferred. A minimum of 15 years of experience in pharmaceutical or medical device regulatory affairs is required.
Experience Required
Minimum 10 year(s)
Affiliate Head of Quality and Regulatory Affairs at F. Hoffmann-La Roche Ltd - Poland
Hod HaSharon, Center District, Israel - Full Time
Skills Needed
Quality Management, Regulatory Affairs, Iso 9001:2015, Auditing, Gmp, Gdp, Ivdr, Mdr, Capa, Training, Stakeholder Engagement, Process Improvement, Leadership, Communication, Life Sciences, Diagnostics, Healthcare
Specialization
Candidates should have a BA/BS, MS, or PhD in Life Sciences, Medical, or Engineering fields with 5-10 years of relevant experience. Expertise in ISO standards and a strong understanding of healthcare systems in Israel are essential.
Experience Required
Minimum 5 year(s)
Executive Manager, Government & Industry Affairs at Commonwealth Bank
Sydney, New South Wales, Australia - Full Time
Skills Needed
Policy Campaigning, Advocacy, Public Policy Development, Analytical Skills, Communication Skills, Relationship Management, Interpersonal Skills, Judgement, Discretion, Professionalism, Team Culture, Risk Management, Research, Monitoring, Political Analysis, Regulatory Analysis
Specialization
Candidates should have expertise in policy campaigning and advocacy, with strong analytical and communication skills. Experience in government, banking, finance, or a related field is highly regarded.
Experience Required
Minimum 5 year(s)
Nevada Gold Mines - Community Affairs Specialist at Barrick
, , - Full Time
Skills Needed
Community Engagement, Public Relations, Communication Skills, Team Player, Crisis Management, Stakeholder Engagement, Organizational Skills, Education Programs, Mining Industry Knowledge, Environmental Regulations, Computer Proficiency, Independent Work, Multi Tasking, Matrix Structure Support
Specialization
Candidates must have a bachelor's degree in a relevant field and three years of experience in community relations or six years of applicable experience. Strong communication skills and the ability to work independently and as part of a team are essential.
Experience Required
Minimum 2 year(s)
ELECTRIC/ELECTRONIC REGULATORY AFFAIRS TECHNICIAN at Eurofins
Barcelona, Catalonia, Spain - Full Time
Skills Needed
Regulatory Compliance, Electrical Products, Electronic Products, Bazaar Products, Toy Regulations, Technical Documentation, Regulatory Monitoring, Cen Cenelec Standards, Electrical Safety, Legal Framework Analysis, Consulting, Microsoft Excel, Organization, Methodical Work, Teamwork
Specialization
Candidates must have a higher vocational degree specializing in electrical/electronics, along with knowledge of the European and national regulatory-legal framework for the electrical/electronic sector and electrical safety in consumer products. A minimum of 2 years of experience, native Spanish, and medium-high level English are required.
Experience Required
Minimum 2 year(s)
Government Affairs and Community Relations Manager at Brightspeed
Columbus, Ohio, United States - Full Time
Skills Needed
Government Affairs, Community Relations, Stakeholder Engagement, Permitting, Regulatory Compliance, Public Policy, Advocacy, Cross Functional Coordination, Relationship Building, Communication, Problem Solving, Organizational Skills, Analytical Skills, Microsoft Office Proficiency, Telecommunications Knowledge, Broadband Deployment
Specialization
Candidates must have a Bachelor's degree in a related field or equivalent experience, along with a minimum of three years in government affairs, public policy, or community relations. Essential qualifications include being based in the Columbus, OH area and possessing strong knowledge of state/local government processes and excellent relationship-building skills.
Experience Required
Minimum 2 year(s)
Director of Regulatory Affairs & Quality Control at SINTX
Salt Lake City, Utah, United States - Full Time
Skills Needed
Regulatory Affairs, Quality Control, Fda Submissions, Risk Management, Quality Management System, Additive Manufacturing, Biomaterials, Lean Six Sigma, Clinical Collaboration, Product Launch, Lifecycle Management, Cross Functional Leadership, Strategic Planning, Supplier Audits, Post Market Surveillance, Compliance
Specialization
Candidates must have a bachelor's degree in a relevant field and at least 10 years of experience in regulatory affairs and quality within medical devices or biomaterials. Direct experience with FDA submissions and strong knowledge of quality standards is essential.
Experience Required
Minimum 10 year(s)
H&M Department Manager- Dayton Mall at H&M Group
Dayton, Ohio, United States - Full Time
Skills Needed
Leadership, Team Management, Sales Analysis, Profit Optimization, Customer Experience, Visual Merchandising, Recruitment, Performance Management, Fashion Awareness, Trend Analysis, Cost Efficiency, Scheduling, Operational Routines, Stock Management, Team Collaboration, Communication
Specialization
Successful candidates must be strong, ambitious leaders who enjoy taking responsibility, possess effective communication skills, and are analytical solution finders capable of managing statistics and numbers. The role requires being achievement-oriented, motivated by performance, and truly customer-centric.
Experience Required
Minimum 2 year(s)
Packing Clipping Department Worker 3 at KCARC
Vincennes, Indiana, United States - Full Time
Skills Needed
Attention To Detail, Quality Control, Teamwork, Multitasking, Time Management, Safety Compliance, Communication, Problem Solving
Specialization
Candidates should have the ability to maintain a flexible schedule and establish working relationships. Prior manufacturing experience and knowledge of a sewing facility are helpful but not required.
Bakery Department Clerk - Full Time at Ridley’s Family Markets
Rupert, Idaho, United States - Full Time
Skills Needed
Customer Relations, Communication, Product Knowledge, Pricing, Merchandising, Quality Control, Teamwork, Training, Sales, Display Management, Order Management, Suggestive Selling, Cost Control, Behavioral Skills, Bakery Products, Attention To Detail
Specialization
Candidates should possess knowledge of bakery items and be capable of pricing and merchandising products. Strong communication skills and the ability to work collaboratively are essential.