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Clinical Trials Operations Manager
2 months ago
DOCS Dermatology is a leading provider in the field of dermatology, recognized for its extensive network of specialists and commitment to patient care. With over 186 providers across multiple locations, we have been dedicated to delivering high-quality dermatologic services for decades.
Position Summary
The Clinical Research Manager plays a crucial role in guiding a talented team through the complexities of clinical trials, contributing to significant innovations in dermatology and skin care research.
This position presents a unique opportunity to utilize your expertise and leadership capabilities to enhance our research initiatives and uphold our dedication to outstanding patient care and clinical proficiency.
Key Responsibilities
- Lead and manage the research team throughout all stages of clinical trials, ensuring adherence to compliance, effectiveness, and excellence.
- Work closely with the Clinical Research Director to oversee the operations of the research center.
- Ensure protocol compliance, patient recruitment, and successful trial execution.
- Devise and implement strategies for effective participant recruitment and retention.
- Collaborate with sponsors to prepare and finalize study contracts and budgets.
- Manage research budgets and contracts with precision.
- Guarantee compliance with federal regulations and ethical standards in all research activities.
- Facilitate communication among sponsors, investigators, and participants to enhance research efficiency.
- Maintain accurate records and documentation in line with GCP and IRB standards.
- Prepare accrual and revenue reports for corporate financial reconciliation.
- Oversee invoicing to sponsors for associated expenses.
- Conduct staff training and evaluations to promote a cohesive and productive team environment.
Minimum Qualifications
- High School diploma or equivalent; certification as a Clinical Research Coordinator or Clinical Research Associate is highly preferred.
- 5+ years of experience in a clinical research environment.
- Exceptional attention to detail and a strong commitment to research integrity.
- Demonstrated organizational and communication skills, with the ability to lead and collaborate effectively.
- Ability to adapt priorities based on evolving business needs while maintaining confidentiality.
- Proficiency in Microsoft Office and familiarity with Electronic Medical Record (EMA) systems.
Physical Demands
While performing the duties of this role, the employee may be required to sit or stand for extended periods. Frequent movements of the wrists, hands, and fingers are necessary due to computer work.
Equal Opportunity Employer:
We are committed to creating a diverse environment and are proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, genetic information, disability, protected veteran status, or any other legally protected group status.