Clinical Project Manager

Working Nomads; United States; Remote; USD 80,000 - 120,000; Full time

Job summary

A biopharmaceutical company in the United States is seeking a Clinical Project Manager for home-based work, ensuring compliance in multi-center studies. Candidates should hold a bachelor's degree in a relevant field and have clinical research experience. The role involves planning, coordinating study activities, and communication with sponsors. Travel up to 30% is expected.

Qualifications

• Bachelor's degree required, preferably in science or nursing.
• Clinical research experience as a CRA or Research Coordinator preferred.
• Experience in business development processes is advantageous.

Responsibilities

• Lead multi-center studies ensuring compliance with regulations.
• Plan and procure team resources to complete study activities.
• Coordinate activities with laboratories and service providers.
• Review and negotiate site budgets and contracts.

Skills

Clinical research experience

Excellent problem-solving skills

Ability to work across multiple projects

Experience with renal and hepatic impairment studies

Experience with infectious disease studies

Education

Bachelor's degree in science or biomedical discipline

Job description

Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.

Position Summary:

Celerion is looking for a Clinical Project Manager who will be responsible for the independent management of multi-center site activities ensuring compliance to protocol, ICH Good Clinical Practices, Standard Operating Procedures and regulatory and local requirements.

This role will be home based anywhere in the United States. Due to our international footprint, schedule flexibility is important. This position will travel roughly 30% primarily in the US, but could include Europe on an as needed basis.

Key responsibilities include:

• Lead the initiation, maintenance and close out activities of multi-center studies in accordance with the protocol, relevant SOPs, Good Clinical Practice, international standards, and regulatory requirements
• Plan and procure team resources as needed to complete study activities according to scope, budget, and timeline
• Develop and/or oversee development of study plans such as project management (including communication), monitoring, risk management, data management and safety plans
• Coordinate activities with central laboratories and other external service providers/vendors
• Review and negotiate site budgets and contracts
• Initiate and participate in the development of change orders to sponsor and/or site contracts and budgets
• Maintain appropriate and effective communication with sponsor, external service providers, and other internal departments to ensure successful project completion

Requirements:

• Bachelor's degree required, preferably in science, nursing, other biomedical discipline, or equivalent
• Clinical research experience as a CRA or Research Coordinator is preferred
• Experience in support of business development processes; including budgets, proposals and bid defense planning and execution
• Ability to work across multiple projects
• Experience with renal and hepatic impairment, infectious disease and tobacco studies is an asset
• Flexible and willing to travel up to 30% (regional)
• Excellent problem-solving and decision making skills

Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.