Clinical Research Project Manager, Men's Health Initiative
hace 2 semanas
Job Summary
The Clinical Trial Project Manager will oversee study recruitment and retention activities for federal and industry-sponsored clinical trials across various therapeutic areas, including men's health studies. This role will work closely with study PIs, research team members, and other stakeholders to develop and implement study-specific recruitment strategies, maximize the utilization of existing methods, and pioneer new innovative approaches to enhance overall recruitment efforts and enrollment efficiency.
Key Responsibilities
- Develop and lead the implementation of clinical trial recruitment strategies and social media postings for single-site and multi-site clinical trials.
- Prepare summary reports for project teams regarding enrollment status and study progress.
- Oversee the preparation of study-specific recruitment materials for IRB submissions.
- Contribute to the development of study-specific documents, such as case report forms, eligibility screening scripts, and questionnaires.
- Identify protocol challenges and opportunities for recruitment and retention.
- Initiate discussions to promote effective use of recruitment and retention tools available to the site or study.
- Prompt site follow-up on pre-identified participants and screen failed patients.
- Construct and maintain study databases, oversee data entry, and assure adherence to intended timelines and achievement of study goals.
- Develop and implement measures to improve efficiency in recruitment operations.
- Direct management responsibility for study personnel, including senior research coordinators, research assistants, and undergraduate/graduate student assistants.
Requirements
- Master's degree
- Minimum 3-5 years of progressively more responsibility clinical research recruitment experience
- Minimum 3 years prior experience in management responsibility of research staff required
- Proven record of successful problem-solving and decision framing skills pertaining to clinical trial recruitment
- Proficiency in Microsoft Office applications (e.g., Outlook, Word, and Excel)
- Familiarity with electronic data capture (EDC) systems preferred (e.g., REDCap)
- Intermediate knowledge of medical terminology preferred
- Certifications in the Protection of Human Subjects and Good Clinical Practice, per institutional and regulatory guidelines
Skills and Abilities
- Excellent organizational skills and ability to effectively manage research personnel, time, and prioritize workload
- Strong oral and written communication skills
- Excellent critical thinking and problem-solving skills
- Analytical skills necessary to accurately interpret and implement complex policy
- Comfortable working both independently and as part of a team
- Excellent interpersonal and relationships skills, ability to build rapport and interact effectively with a broad array of people from diverse cultural and educational backgrounds
- High degree of professionalism, discretion, and confidentiality
- Ability to supervise and train staff effectively
- Strong database management, analytical, and computer skills
BWH is an Affirmative Action Employer.
We are an equal opportunity employer and welcome applications from diverse candidates.
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