Medical Director

2 weeks ago

Cambridge, United States Integrated Resources, Inc Full time
Client is seeking an experienced Director, Clinical Development to join our team and embark on a unique journey of advancing our clinical development programs in rare cholestatic liver disease. In this position, you will be an integral part of the clinical development team, supporting the execution of late-stage clinical studies. The ideal candidate will have outstanding communication skills, attention to detail, and the ability to thrive independently in a highly innovative and fast-paced environment. Provide medical expertise and leadership in designing and implementing clinical development strategies aligned with company objectives.

Job Responsibilities
Clinical Trial Strategy and Design:
Collaborate with cross-functional teams (including Clinical Operations, Biostatistics Regulatory Affairs, Patient Safety, and Pharmacology/Pharmacometrics) to design and implement clinical trials
Ensure that clinical trial protocols align with scientific and regulatory requirements
Oversee patient recruitment, data collection, and safety monitoring during trials

Medical Oversight:
Provide medical expertise to study teams, investigators, and site staff
Review and interpret clinical trial data, including safety and efficacy endpoints
Make informed decisions based on medical insights to optimize trial outcomes
Regulatory Interactions:
Engage with regulatory agencies (such as the FDA or EMA) during clinical development
Prepare and submit clinical trial applications, investigator brochures, and other regulatory documents
Address regulatory queries and ensure compliance with guidelines

Clinical Development Strategy:
Contribute to the overall clinical development strategy for the company s pipeline products
Identify opportunities for expansion into new indications or patient populations
Evaluate scientific literature and competitive landscape to inform strategic decisions
KOL Engagement and Scientific Communication:
Build relationships with Key Opinion Leaders (KOLs) in relevant therapeutic areas
Present clinical trial results at scientific conferences and meetings
Collaborate with external experts to enhance product understanding
Team Leadership and Mentorship:
Depending on the candidate's expertise level, the responsibilities may include leading a team of clinical professionals, including Clinical Scientists and Medical Monitors
Effectively fosters productive and collegial working relationships with internal and external stakeholders in a cross-functional, matrix environment

Additional Info
This is a hybrid/remote role for the candidate; however, if the candidate is local to the area, the candidate will be expected to come into the office occasionally
Advanced scientific degree (MD or DO, PhD, PharmD)
Must have experience leading all aspects of clinical trials
Must have pharma clinical trial /R&D experience (3-5 years)
Rare disease experience and or gastroenterology/hepatology experience in clinical development preferred
Solution- and results-oriented, with a sense of urgency
Must have experience and be willing to perform in-depth clinical data review

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