Job Summary: The Clinical Project Manager (CPM) will oversee and manage all aspects of clinical trials within our Biotech Client's team. This role involves planning, executing, and closing clinical studies, ensuring compliance with regulatory requirements, and maintaining high-quality standards. The CPM will collaborate with cross-functional teams to achieve project goals, meet timelines, and stay within budget.
Key Responsibilities:
Project Planning and Management:
Develop and manage detailed project plans, including timelines, budgets, and resource allocation.
Identify project risks and implement mitigation strategies.
Proactively managing operational aspects of clinical projects;
Ensuring clinical studies are conducted according to the study protocol, SOPs, ICH/GCP regulations, and study-specific manuals and procedures;
Contributing to the preparation of clinical documents such as protocols, informed consent forms, and study plans, guides, and manuals;
Participating in the development of clinical parts of regulatory documents, such as the IND, IB, and briefing documents
Qualifications:
Bachelor’s degree in Life Sciences, Clinical Research, or a related field; Master’s degree or equivalent is a plus.
2-4 years of experience in clinical project management within the pharmaceutical or biotechnology industry.
Strong understanding of clinical trial processes, regulatory requirements, and Good Clinical Practice (GCP).
Proven experience in managing complex clinical trials from initiation through to completion.
Excellent project management skills, including experience with project management software and tools.
Reach out directly if you are looking to take your career to the next level:
cayla@peoplewithchemistry.com
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Project Management, Research, and Science
Industries
Pharmaceutical Manufacturing and Biotechnology Research
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