Clinical Project Manager II (CTM role) - 3 days a week in Uxbridge

Syneos Health; Uxbridge; On-site; GBP 80,000 - 100,000; Full time

Job summary

A healthcare consulting firm in Uxbridge is seeking an experienced project manager to oversee clinical research studies. The role requires managing timelines, budgets, and compliance with regulations. The ideal candidate has a Bachelor's degree in a relevant field and strong organizational skills. This position presents an opportunity to work in a collaborative environment, ensuring quality in project deliverables.

Qualifications

• Requires a Bachelor's degree or equivalent in a relevant field.
• Preferred experience in clinical research organization (CRO) and therapeutic areas.
• Strong organizational and time management skills.

Responsibilities

• Manage projects overseeing clinical research studies compliant with GCP.
• Liaison between Company and Customer for study launch and conduct.
• Ensure quality, timelines, and budget management.

Skills

Project Management

Communication

Organizational skills

Time management

Education

Bachelor's Degree in life sciences, Medicine, Pharmacy, Nursing or equivalent

Job description

Responsibilities

• Project Leadership and Delivery. Manages a project as a project manager overseeing interdisciplinary clinical research studies and ensures compliance with GCP, relevant SOPs, and regulatory requirements.
• Acts as a primary liaison between the Company and the Customer to ensure timely study launch, conduct, and closeout according to the Customer's and the Company's contractual agreement.
• Lead project team to ensure quality, timelines and budget management.
• Accountable for the financial performance of each project. Coordinate activities and deliverables of all study conduct partners and proactively identify and manage issues.
• Ensure studies are conducted in compliance with GCP, relevant SOPs and regulatory requirements. Accountable for all project deliverables for each project assigned.
• Responsible for quality and completeness of TMF for assigned projects.
• Accountable for maintenance of study information on a variety of databases and systems.
• Responsible for study management components of inspection readiness for all aspects of the study conduct. Oversight for development and implementation of project plans.
• Plan, coordinate and present at internal and external meetings. Prepare project management reports for clients and management.
• Develop contingency planning and risk mitigation strategies to ensure successful delivery of study goals.
• Develops strong relationships with current clients to generate new and/or add-on business for the future.
• May participate in bid defense meetings where presented as potential project manager.
• May be required to line manage other project management team members and clinical monitoring staff.

Qualifications

• Bachelor's Degree (or equivalent) in life sciences, Medicine, Pharmacy, Nursing or equivalent combination of education and experience.
• Clinical research organization (CRO) and relevant therapeutic experience preferred. Strong knowledge of Good Clinical Practice/ICH guidelines and other applicable regulatory requirements.
• Strong organizational skills.
• Strong ability to manage time and work independently.
• Direct therapeutic area expertise.
• Ability to embrace new technologies.
• Excellent communication, presentation, interpersonal skills, both written and spoken.
• Ability to travel as necessary (approximately 25%).

Syneos Health is an equal opportunity employer and complies with applicable laws ensuring non-discrimination in employment. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.