Salary: $190,000-$215,000
Associate Director Clinical Operations
Boston, MA (Hybrid)
Job Description
EPM is partnered with a cutting-edge biotech firm at the forefront of revolutionizing autoimmune disease treatment. Leveraging groundbreaking advancements in immunology, their proprietary therapies target the root causes of autoimmune disorders, providing unprecedented precision and efficacy. They are dedicated to transforming lives by developing innovative solutions that not only alleviate symptoms but also halt disease progression. With a commitment to scientific excellence, the team is poised to redefine the landscape of autoimmune healthcare, offering hope and relief to millions worldwide. Join the team in shaping the future of autoimmune disease management and ushering in a new era of well-being.
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 autoimmune 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
