Clinical Program Manager
2 weeks ago
Key collaborators are the Clinical Lead for site management, the Project Vendor Manager, the Project Management Analyst for project coordination, tracking and financial analysis, and the Site Activation Manager an expert in start-up.
IQVIA's global footprint presents opportunities to develop your career.
Responsibilities include:
- Manage Clinical Team (CT) agendas, information, documentation, and team communications to ensure timely and accurate dissemination of the CT strategy and operational status.
- Partner with cross-functional leads for the program within Global Development and outside of Global Development such as regulatory, finance, clinical supplies, Biomarker depts and Global Medical safety to ensure appropriate communication and escalations and resolutions around risks and issues.
- Manage the governance infrastructure and reporting with co-development partners and or other external partners as directed by the GPL.
- Lead global cross-functional project team delivery, accountable for achievement of milestones and quality of contracted scope.
- Serve as the primary contact with the customer for progress and governance.
- Develop study management plans and ensure consistent use of study tools, training materials and compliance with standard processes, policies and procedures.
- Anticipate risk and implement mitigation strategies.
- Manage study team assignments, accountability and resource requirements.
- Ensure the study budget is managed proactively including scope changes and financial systems are accurate.
Profile Required:
- A minimum of a bachelor's Degree or equivalent work experience is required.
- Post-Graduate degree in Project Management or business is preferred.
- Professional Project Management certification is preferred.
- A minimum of 5 years industry/CRO/business experience is required in clinical drug development and/or clinical operations, clinical R&D experience preferred.
- A minimum of 3 or more years' experience in Project Management is preferred.
- Prior experience leading a cross-functional global teams is required.
- Demonstrated ability to resolve conflict and influence teams without direct authority.
- Successful experience in planning and management of governance bodies is preferred.
- Proficient in MS Project is required.
- Global project management experience within the drug development industry, with previous CRO experience; familiarity with highly complex projects.
- In-depth therapeutic knowledge in one of our key therapeutic areas including Internal Medicine, Central Nervous System, Gastroenterology, Immunology & Women's Health, Cardiovascular Renal Metabolic, Early Clinical Development or Oncology; Oncology preferred.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
We are a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare – and human health – forward.
No matter your role, everyone at IQVIA contributes to our shared goal of improving human health.
We are an equal opportunity employer and a world leader in using diversity to drive innovation and growth.
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