Baptist Health is the region's largest not-for-profit healthcare organization, with 12 hospitals, over 28,000 employees, 4,500 physicians and 200 outpatient centers, urgent care facilities and physician practices across Miami-Dade, Monroe, Broward and Palm Beach counties. With internationally renowned centers of excellence in cancer, cardiovascular care, orthopedics and sports medicine, and neurosciences, Baptist Health is supported by philanthropy and driven by its faith-based mission of medical excellence. For 25 years, we've been named one of Fortune's 100 Best Companies to Work For, and in the 2024-2025 U.S. News & World Report Best Hospital Rankings, Baptist Health was the most awarded healthcare system in South Florida, earning 45 high-performing honors.
What truly sets us apart is our people. At Baptist Health, we create personal connections with our colleagues that go beyond the workplace, and we form meaningful relationships with patients and their families that extend beyond delivering care. Many of us have walked in our patients' shoes ourselves and that shared experience fuels out commitment to compassion and quality. Our culture is rooted in purpose, and every team member plays a part in making a positive impact - because when it comes to caring for people, we're all in.
Description:
The MCI Research Data Management Coordinator is responsible for the setup, implementation, and management of clinical trial databases for all applicable clinical trials at MCI. These responsibilities include: Database design and setup, Case Report Form (CRF) design, programming and validation of edit checks and User Acceptance Testing (UAT). Perform data monitoring and query generation. Provide, review, and verify data outputs. Additionally, the development of data management documents required for each clinical trial (e.g. eCRF Completion Guidelines, Data Monitoring Plan, Data Validation Plan, etc.). The MCI Research Data Management Coordinator ensures compliance with BHSF policies, applicable federal, state, and local laws, and applicable regulations and guidelines regarding the collection of clinical and research data. Estimated pay range for this position is $20.94 - $27.22 / hour depending on experience.
Qualifications:
Degrees:
Additional Qualifications:
- Clinical Research Certification (CCRC-Certified Clinical Research Coord or CCRP-Certified Clinical Research Professional) preferred.
- Individual with high level computer skills, legal and or clinical research background to work in intensive high volume regulatory environment.
- College graduate preferred.
- Must be detail oriented, very organized but able to multitask to handle high volume paperwork.
- Essential: Excellent interpersonal skills/maturity required for both telephone and direct contact with customers, physicians and hospital personnel.
- Must be able to work independently and efficiently without constant supervision to complete tasks by deadlines and contribute to the department goals as needed.
Minimum Required Experience: 1 year. BLS and CITI required
EOE, including disability/vets
