Salary: $175,000-$200,000
Associate Director Clinical Operations
Boston (Hybrid)
Job Description
Join an innovative biotech company at the forefront of cutting-edge research dedicated to tackling rare diseases. Their unwavering commitment to innovation drives them to the frontlines of scientific discovery, where they focus their energies on an extraordinary mission: combating rare diseases that have long been neglected by traditional pharmaceutical approaches. What sets them apart is their audacious spirit, tireless dedication, and the belief that no challenge is insurmountable. They stand at the intersection of cutting-edge science and compassionate care, working tirelessly to provide hope where it has been scarce and solutions where they have been elusive. As an Associate Director of Clinical Operations, you will be an integral part of our mission-driven team.
Responsibilities
- Identify and proactively address potential risks and issues in clinical trials, implementing mitigation plans to ensure trial success
- Provide leadership and mentorship to clinical operations teams, fostering a collaborative and high-performance work environment while managing and developing talent within the department
- Collaborate with cross-functional teams to develop and execute clinical trial strategies aligned with the company's goals and objectives
- Ensure that all clinical operations comply with regulatory requirements and industry standards, maintaining the highest quality standards in study conduct and documentation
- Oversee relationships with CRO's, vendors, and external partners, ensuring their performance aligns with project objectives and budgets
Qualifications
- 8+ years of hands-on experience in clinical operations within the biotech or pharmaceutical industry, including direct involvement in planning and managing clinical trials
- A deep understanding of rare disease clinical trials, including knowledge of the unique challenges and considerations associated with these trials, is highly desirable
- At least a bachelor's degree in a relevant life sciences field
- Excellent verbal and written communication skills, including the ability to convey complex scientific and clinical information to both technical and non-technical stakeholders
- Proficiency in regulatory compliance and an in-depth understanding of international regulations and guidelines related to clinical trial conduct
Benefits
- Medical, dental, vision insurance
- 401(k)
- PTO and Holidays
