Clinical Research Data Supervisor
Job Description
The Clinical Research Data Operations Supervisor is pivotal in ensuring a safe, secure, and healthy work environment. This role involves leading the hiring process, developing the team through one-on-one discussions, and managing the performance of research team members. You will collaborate with Clinical Research Supervisors to oversee the daily activities of the clinical research team, ensuring productivity and effective personnel scheduling. As an expert resource, you will address any barriers during operations and monitor the quality of data operations.
Responsibilities
Ensure a safe, secure, and healthy work environment.
Lead the hiring process, including applicant review and selection.
Facilitate team development through one-on-one discussions.
Manage performance of research team members, providing feedback and conducting Talent Care discussions.
Collaborate with Clinical Research Supervisors to oversee daily activities of the research team.
Supervise team workflow productivity and maintain staffing schedules.
Serve as an expert resource for the research team.
Monitor and evaluate data operations quality, reviewing monitor follow-up visit letters and sponsor reports.
Essential Skills
Data management
Oncology
Clinical research
Clinical research data
Supervision
EDC (Electronic Data Capture)
Data collection
Data review
Bachelor's Degree in Healthcare Administration, Research, or related field with at least 2 years of clinical research experience
Associate's Degree in Healthcare Administration, Research, or related field with at least 3 years of clinical research experience
Preferred: Master's degree in Healthcare Administration, Research, or related field
Preferred: 5 years of clinical research experience with increasing management responsibilities
Advanced training/experience in data-related items, databases, and various EDC systems
Work Environment
The role primarily involves working onsite, with occasional travel to other locations as necessary.
Pay and Benefits
The pay range for this position is $90000.00 - $105000.00/yr.
together. Across every office, exam and patient room, we're committed to providing individualized, holistic care. This is our Christian mission, and it inspires us to help make communities healthier and happier.
Regulatory Specialist I - AdventHealth Orlando
All the benefits and perks you need for you and your family:
Benefits from Day One
Paid Days Off from Day One
Student Loan Repayment Program
Career Development
Whole Person Wellbeing Resources
Mental Health Resources and Support
Pet Insurance*
Workplace Type
This is a fully onsite position in Orlando,FL.
Application Deadline
This position is anticipated to close on Jun 20, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.