Project Data Manager - Europe at Allucent

, , Ireland -

Full Time

Start Date

Immediate

Expiry Date

07 May, 26

Salary

0.0

Posted On

06 Feb, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Project Leadership, Clinical Data Management, End-to-End Data Management, Database Design & Set-up, Data Cleaning, Regulatory Requirements, Biometrics Projects, Risk Management, Vendor Management, Budget Management, Mentoring, ICH-GCP Knowledge, 21CFR11 Knowledge, EDC Systems, CDISC Conventions, Sponsor Communication

Industry

Pharmaceutical Manufacturing

Description

Lead clinical data. Partner with sponsors. Deliver quality trials. We are looking for a Project Data Manager (PDM) to join our Data Management A-team at Allucent. As a Project Data Manager, you are responsible for leading and coordinating end-to-end data management activities across clinical trials and biometrics stand-alone projects, ensuring high-quality, compliant, and timely delivery of clinical data. At Allucent™, we are dedicated to helping small and mid-sized biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. The role You will lead and oversee data management activities, timelines and finances of the Allucent Data Management (DM) department. Manage and coordinate DM deliverables from database design & set-up, through cleaning and reporting to database locking, ensuring that the completeness, accuracy and consistency of clinical data meet the quality standards and regulatory requirements for analysis and reporting. You are responsible for the overall coordination and management of Data Management/Biostats standalone projects, large and complex trials and/or multiple projects belonging to one client. You work closely with sponsors, vendors, and internal teams to ensure data is collected, cleaned, reviewed, and delivered to the highest standards. You combine hands-on clinical data management expertise with strong project leadership, keeping timelines, scope, quality, and budgets on track. Your main responsibilities will be: Lead and oversee Data Management activities from database design through to database lock Act as the primary point of contact for Data Management for sponsors, vendors, and internal stakeholders Plan, coordinate, and deliver biometrics and clinical data projects according to scope, timelines, and contract Establish and maintain clear communication, escalation, and risk management plans Lead internal and external meetings, including Kick-Off Meetings and sponsor discussions Manage vendors and support vendor selection and oversight where required Oversee project budgets, financial health, and monthly status reporting Supervise and support junior Data Management team members, ensuring quality and development You are an experienced clinical data management professional who enjoys taking ownership, working closely with clients, and bringing structure to complex studies. You will bring the following skills and experience: Life science, healthcare degree and/or combination of education and experience Minimum 8 years of relevant work experience in Clinical Data Management or related experience within Biometrics Minimum 8 years of relevant experience in related clinical trials environment Thorough knowledge and understanding of ICH-GCP, 21CFR11 data privacy (GDPR/HIPPA) guidelines and awareness of local/regional requirements Experience as DM Lead on several studies and experience in covering all phases of a clinical study (start up, conduct and database lock). Worked on multiple indications and clinical phases (I-IV) Thorough understanding of EDC (Medidata or Veeva) database components and experience in technical data management practices (validation plans, testing, and documentation Experienced in CDISC conventions, i.e., CDASH, TAUG models and hands on experience implementing these models Confidence working directly with sponsors and external vendors A collaborative mindset and the ability to mentor and guide others Strong communication skills in English and comfort working in a global environment Comprehensive benefits package per location Competitive salaries per location Departmental Study/Training Budget for furthering professional development Flexible Working hours (within reason) Leadership and mentoring opportunities Participation in our enriching Buddy Program as a new or existing employee Internal growth opportunities and career progression Financially rewarding internal employee referral program Access to online soft-skills and technical training via GoodHabitz and internal platforms Eligibility for our Spot Bonus Award Program in recognition of going above and beyond on projects Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees About Allucent Our mission is to help bring new therapies to light. When you work at Allucent, that means applying your unique skill set, expertise, and knowledge to build partnerships with our clients in their pursuit to develop new, life-improving treatments. If you're passionate about helping customers develop new pharmaceuticals and biologics; have an entrepreneurial spirit; and ready to join other science, business, and operations leaders, we would love to get to learn more about how we can help each other grow. Apply now! Ready to grow your data management career while contributing to meaningful research to Allucent, apply today or reach out to Yael Kokernoot, Sr. Manager Talent Acquisition (yael.kokernoot@allucent.com) for more information. Disclaimers: *Our in-office work policy encourages a dynamic work environment, prescribing 2 days in office per week for employees within reasonable distance from one of our global offices. “The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively “Allucent”). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources.” #LI-YK1 #LI-remote

Responsibilities

The Project Data Manager is responsible for leading and coordinating end-to-end data management activities across clinical trials and biometrics stand-alone projects, ensuring high-quality, compliant, and timely delivery of clinical data. This includes overseeing data management activities, timelines, and finances, from database design through to lock, while managing deliverables from internal teams and vendors.