Clinical Project Manager/Clinical Project Manager at Precision for Medicine

, , Singapore -

Full Time

Start Date

Immediate

Expiry Date

20 Apr, 26

Salary

0.0

Posted On

20 Jan, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research, Project Management, Budget Management, Risk Management, Quality Management, Communication, Interpersonal Skills, Organizational Skills, Attention to Detail, Microsoft Office, eTMF, EDC, CTMS, Cross-Functional Management, Analytical Skills, Presentation Skills

Industry

Pharmaceutical Manufacturing

Description

Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing life-changing therapies to patients. What sets us apart is the way we integrate clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences. We have a strong focus on Oncology and Rare Disease. Position Summary: The Senior/Project Manager plans, directs, coordinates, and delivers activities for designated clinical-study projects to ensure that project objectives of quality, scope, cost, and time are accomplished. PM will either manage regional trials (moderate complexity) and/or supportive role in managing complex global trials. The essential functions below will describe the PM acting in a primary / lead PM role on a study. When in a supportive role on a global study, the essential functions will be delegated by the Global Lead. Essential functions of the job include but are not limited to: • Serve as primary point-of-contact and primary escalation point to the client • Coordinate and oversees all functional services including external vendors to the established timeline and budget • Manage the study budget, ensuring project remains within scope and that any out of scope activities are identified early and handled as appropriate. • Ensure functional areas are fully aware of the study scope and are managing the scope for their functional areas accordingly. • Manage the financial health of assigned studies, including oversight of the project profitability, billable project hours, and compliance with on time, accurate billing and forecasting to support business objectives. • Develop robust and comprehensive project plans, including timelines and proactive risk management and mitigation, to guide all parameters of trial execution with consistency and quality • Ensure Quality management for assigned projects, including eTMF Inspection readiness, implementation of quality notification incident forms and / or corrective and preventative action plans to address any quality findings. • Maintain integrated collaboration with all functional operations in the delivery of the program and review as necessary of other study documentation • Establish tracking metrics to monitor trial and team progress towards project goals • Prepare project status updates and report on progress to clients and senior management, including reporting on key performance indicators, offering solutions and opportunities as they arise • Lead both internal and client meetings and set expectations for the project team • Communicate effectively with client and Precision management to relay protocol/study issues including any deviations and implements necessary actions in response to those issues • Ensure study specific training is implemented in collaboration with functional areas and ensure study specific training compliance for the duration of the project • Support business development and marketing activities as appropriate, including travel to Bid Defence meetings as required • Perform other duties as assigned by management • Remain compliant with organisational training, time-reporting and any other administrative duties as required • Provides on-going feedback for functional team members including annual performance reviews • Ability to travel domestically and internationally including overnight stays Qualifications: Minimum Required: • Degree or equivalent combination of education/experience in science or health-related field. Advanced degree preferred • Minimum of 3-7 years of clinical research experience or proven competencies for this position and a minimum of 2-4 years of leading a project • Experience managing regional trials (moderate complexity) and/or supportive role in managing complex global trials Other Required: • Experience with Microsoft Office Products (Outlook, Word, Excel, PowerPoint), Microsoft Project,eTMF, EDC and CTMS • Good communication and interpersonal skills to effectively interface with others in a team setting • Good organizational skills, attention to detail, and a customer service demeanor Competencies: • Demonstrates knowledge of ICH-GCP, relevant Precision SOPs, as well as the ability to implement such items • Working knowledge of project management techniques and tools • Experience working in a cross-functional project management environment • Fundamental understanding of cross-functional management • Fundamental understanding of project planning, risk management and change management with an awareness of appropriate escalation • High level of integrity and must inspire and demand the highest standards from a professional and ethical perspective • Ability to lead and inspire excellence within a study team • Ability to create an environment where study team members have a sense of ownership that will lead to increases in productivity and efficiency • Results oriented, accountable, motivated and flexible • Good time management, negotiation, critical thinking, decision making, analytical and interpersonal skills • Good presentation, verbal and written communications skills • Fundamental understanding of project management software • Experience in pharmaceutical and/or device research required We invite you to learn more about our growing organization serving our clients that are researching ground breaking cancer therapies. We strive to ensure employees feel appreciated for the contributions they make every single day. You will provide input and have your ideas valued and nurtured, impacting positive change for the company. Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice. Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com. It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.

Responsibilities

The Clinical Project Manager plans, directs, coordinates, and delivers activities for designated clinical-study projects to ensure project objectives are met. They serve as the primary point of contact for clients and manage study budgets, timelines, and quality management.