What are the responsibilities and job description for the Senior Director, Global Clinical Program Lead position at Proclinical Staffing?
Senior Director, Global Clinical Program Lead - Permanent - Boston, MA
Ready to lead clinical programs that bring life-changing treatments to the world? Join our client at the forefront of pharmaceutical innovation and make a difference!
Proclinical is seeking a Clinical Development Lead to oversee the design and execution of clinical strategies supporting the development of medicines.
Primary Responsibilities:
In this role, you will provide strategic leadership to cross-functional teams, ensuring high-quality clinical standards and compliance with regulatory guidelines. This position requires expertise in clinical oversight, document authorship, and stakeholder management.
Skills & Requirements:
- Medical degree (MD) with board certification or equivalent in a relevant field (e.g., Cardiology, Neurology, Internal Medicine).
- Strong understanding of pharmaceutical and regulatory development processes.
- Experience in clinical development, including study data review and evaluation.
- Proficiency in leading cross-functional teams and managing complex projects.
- Excellent communication and documentation skills, with experience in regulatory submissions and scientific publications.
The Senior Director, Global Clinical Program Lead's responsibilities will be:
- Design and execute clinical strategies aligned with project goals and product profiles.
- Lead the Clinical Development Team (CDT), managing day-to-day operations, decision-making, and stakeholder engagement.
- Ensure programs comply with Good Clinical Practice (GCP) and International Council for Harmonisation (ICH) regulations.
- Provide clinical oversight during study development and execution, including serving as a medical monitor or overseeing assigned monitors.
- Represent clinical development in cross-functional teams such as Safety Management, Benefit-Risk Assessment, and Evidence Strategy Teams.
- Author or contribute to key documents, including Clinical Development Plans, Investigator Brochures, Study Protocols, and regulatory submissions.
- Review study data to assess safety and efficacy, contributing to development strategies and regulatory interactions.
- Develop abstracts, presentations, and manuscripts based on study findings.
Compensation:
- $40,000 to $42,500 per annum.
If you are having difficulty in applying or if you have any questions, please contact Bo Forsen at b.forsen@proclinical.com
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
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Salary : $40,000 - $42,500