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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 May 28, 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 [email protected] (%[email protected]) for other accommodation options.