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Baptist Health South Florida

Clinical Research Data Project Manager, Research Administration, FT, 8:00A 4:30P

Posted 2 hours ago
$71242.35 - $92615.06 per year
5-10 years experience
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AI Summary

The Clinical Research Data Project Manager is responsible for designing, maintaining, and administering clinical research databases while ensuring data quality standards. They will also develop data management documentation, provide operational leadership, and support end users with troubleshooting and complex reporting.



Baptist Health is the region's largest not-for-profit healthcare organization, with 12 hospitals, over 29,000 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 26 years, we've been named one of Fortune's 100 Best Companies to Work For, and in the 2025-2026 U.S. News & World Report Best Hospital Rankings, Baptist Health was the most awarded healthcare system in South Florida, earning 63 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.

At Baptist Health, we’re committed to supporting our employees at every stage of their journey, both personally and professionally. Our approach is rooted in a “grow our own” philosophy, designed to help our team members build meaningful, long-term careers with us, supported by benefits that make a real difference, including:

  • Career growth and development opportunities, with clear pathways and ongoing support
  • Comprehensive health and wellness resources that go beyond traditional benefits
  • A wellness program that can help employees eliminate their medical plan deductible, reducing out-of-pocket healthcare costs
  • Tuition reimbursement to support continued learning and advancement
  • And so much more
     

Together, these benefits and others reflect our commitment to caring for our people, so they can build fulfilling careers with us while making a meaningful impact every day.

Description:


The Clinical Research Data Project Manager will be responsible for database design, administration, and maintenance, including gathering requirements from the principal investigator, biostatistician, and study management staff to structure and design recruitment and study tracking databases. Identify and develop appropriate data management documents required for each project or clinical trial (e.g., eCRF Completion Guidelines, Data Monitoring Plan, Data Validation Plan). Current systems in use include, but are not limited to, Advarra EDC, REDCap, and MS Excel. In addition, they will manage support requests and administrative needs of database end users, including day-to-day trouble shooting of databases, and requested data reports using complex queries. They will develop standard operating procedures for data collection, entry, validation, and cleansing. The clinical research data manager provides operational leadership to the direction, planning, execution, collection and handling of all clinical data to the highest quality standards while ensuring established standards. Estimated salary range for this position is $71242.35 - $92615.06 / year depending on experience.

Qualifications:


Degrees:
  • Bachelors.
Licenses & Certifications:
  • Collab Inst Training Init.
Additional Qualifications:
  • Bachelor‘s degree in Biostatistics, Computer Science, or related field.
  • Master‘s degree preferred.
  • CITI Certification within 30 days, Certified Clinical Research Coordinator preferred.
  • 3+ years of prior data management & analysis, including previous experience in SAS (or similar coding language or statistical programming tool), is required.
  • Must have ability to interact with statisticians regarding sophisticated data analysis approaches to be implemented.
  • Excellent computer skills, including proficiency with Microsoft toolset (Excel, Word, PowerPoint, Access), Sharepoint, & Microsoft SQL Server is highly preferred.
  • Demonstrated knowledge of clinical research & FDA reporting st&ards, fundamental database design, including relational constructs, query design, database normalization, indexes & constraints.
  • Capability of managing multiple projects simultaneously which includes excellent planning, time management, communication, decision making, organization, & interpersonal skills.
  • Excellent interpersonal skills/maturity required for telephone, email, & direct contact with customers, physicians, & hospital personnel.
  • Must be able to work independently (including a remote setting), efficiently complete tasks, & contribute to department goals as needed.
  • Active membership in professional organizations.
Minimum Required Experience: 5 Years



EOE, including disability/vets

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