What are the responsibilities and job description for the Clinical Operations Site Director position at Biologic-Scientific Research Institute SMO?
Overview
We are seeking a dedicated and experienced Site Director to oversee the operations of our clinical research site. The ideal candidate will possess a strong background in clinical trials management and scientific research, ensuring compliance with FDA regulations and Good Clinical Practice. This role requires exceptional leadership skills to guide the team in delivering high-quality research outcomes while maintaining a focus on patient safety and regulatory adherence.
Responsibilities
- Lead and manage all aspects of clinical trial operations at the site, ensuring adherence to protocols and regulatory requirements.
- Oversee the planning, execution, and reporting of clinical trials, ensuring timelines and milestones are met.
- Collaborate with cross-functional teams including research development, clinical development, and data management to ensure seamless project execution.
- Ensure compliance with FDA regulations and Good Clinical Practice throughout all phases of clinical trials.
- Provide guidance and mentorship to staff, fostering a collaborative environment that promotes professional growth.
- Monitor site performance metrics and implement strategies for continuous improvement in trial execution.
- Facilitate communication between sponsors, regulatory agencies, and internal teams to ensure alignment on project goals.
- Conduct training sessions for staff on clinical trial protocols, procedures, and best practices.
Experience
- Proven experience in clinical trials management with a strong understanding of FDA regulations and Good Clinical Practice.
- Background in scientific research or related fields is highly desirable.
- Proficiency in SAS or similar statistical software is a plus.
- Demonstrated leadership skills with the ability to motivate and manage diverse teams effectively.
- Experience in research development or clinical development is preferred.
- Strong analytical skills with the ability to interpret complex data sets related to clinical trials.
We invite qualified candidates who are passionate about advancing clinical research to apply for this exciting opportunity as a Site Director.
Job Type: Full-time
Benefits:
- 401(k)
- 401(k) matching
- Dental insurance
- Health insurance
- Health savings account
- Life insurance
- Paid time off
- Parental leave
- Retirement plan
- Tuition reimbursement
- Vision insurance
Schedule:
- 10 hour shift
- 8 hour shift
- Day shift
- Evening shift
- Monday to Friday
- Weekends as needed
Supplemental Pay:
- Bonus opportunities
People with a criminal record are encouraged to apply
Ability to Relocate:
- Philadelphia, PA 19104: Relocate before starting work (Required)
Work Location: Hybrid remote in Philadelphia, PA 19104