What are the responsibilities and job description for the Clinical Research Site Director position at Arrow Clinical Trials?
Job Title: Clinical Research Site Director
Location: Daytona Beach, FL
Company: AArrow Clinical Trials
Type: Full-Time
About Us:
Arrow Clinical Trials is a leading clinical research organization dedicated to advancing medical science through innovative clinical trials. We partner with pharmaceutical, biotechnology, and medical device companies to bring promising treatments to patients faster. We are seeking an experienced Clinical Research Site Director to lead and manage our clinical research operations at our site. If you have a passion for clinical research and a proven track record of managing clinical trials, we want to hear from you!
Job Summary:
As the Clinical Research Site Director, you will be responsible for the oversight and management of all clinical trial activities at our site. This role requires a blend of strong leadership, clinical expertise, and project management skills. You will work closely with the study teams, clients, and regulatory bodies to ensure that clinical trials are conducted in accordance with GCP, ICH guidelines, and regulatory requirements.
Key Responsibilities:
- Oversee day-to-day operations of the clinical research site, ensuring trials are completed on time, within budget, and in compliance with regulatory requirements.
- Manage site staff, including recruitment, training, performance management, and career development.
- Ensure that clinical trials are conducted according to protocol, Good Clinical Practice (GCP), and ICH guidelines.
- Maintain relationships with sponsors, CROs, and key stakeholders to ensure successful trial execution.
- Monitor site performance, resolve issues, and optimize processes for efficient trial conduct.
- Ensure accurate documentation and timely submission of regulatory documents, patient records, and trial data.
- Develop and implement strategies for patient recruitment and retention.
- Serve as a key point of contact for sponsors, regulatory agencies, and auditors.
Qualifications:
- Bachelor’s degree in Life Sciences, Nursing, or related field (or equivalent experience).
- At least 5 years of experience in clinical research, with 2 years in a leadership role (Clinical Research Coordinator, Clinical Research Manager, or similar).
- Strong understanding of GCP, ICH guidelines, and regulatory requirements.
- Proven experience in managing clinical trials, including budgeting, staffing, and timelines.
- Excellent communication, organizational, and problem-solving skills.
- Ability to lead and motivate a diverse team in a fast-paced environment.
- Clinical research certifications (e.g., CCRA, CCRC) preferred but not required.
Why Join Us:
- Competitive salary and benefits package
- Opportunity to make an impact in advancing healthcare
- Dynamic and collaborative work environment
- Career growth opportunities in a fast-growing company
How to Apply:
Interested candidates should submit a resume and cover letter detailing their relevant experience to drbillmeier@arrowtrials.com
Arrow Clinical Trials is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
Job Type: Full-time
Pay: $35.00 - $55.00 per hour
Expected hours: 40 per week
Benefits:
- 401(k)
- 401(k) matching
- Dental insurance
- Health insurance
- Life insurance
- Paid time off
- Vision insurance
Medical Specialty:
- Cardiology
- Dermatology
- Endocrinology
- Gastroenterology
- Infectious Disease
- Neurology
- Rheumatology
Schedule:
- 8 hour shift
- No weekends
People with a criminal record are encouraged to apply
Ability to Commute:
- Daytona Beach, FL 32117 (Required)
Ability to Relocate:
- Daytona Beach, FL 32117: Relocate before starting work (Required)
Work Location: In person
Salary : $35 - $55