• Clinical Research Supervisor (Oncology)

    Actalent (Orlando, FL)


    Job Title: Clinical Research Coordinator (Oncology)Job Description

     

    The Clinical Research Coordinator plays a crucial role in overseeing the conduct of industry-sponsored and investigator-initiated clinical trials. This position ensures compliance with trial protocols, FDA regulations, and ICH/GCP guidelines. The Coordinator may function as a clinical study coordinator when needed and is responsible for training, mentoring, and developing the clinical study coordinators and research staff across various locations. The role involves close collaboration with managers and leaders to facilitate the initiation and completion of clinical research studies.

    Responsibilities

    + Supervise day-to-day activities of the clinical research team, ensuring productivity and maintaining staffing schedules.

    + Ensure safe care delivery while respecting the dignity and rights of all patients and participants.

    + Act as a service line expert and resource for the research team, addressing operational barriers.

    + Monitor and evaluate the quality and safety of clinical operations in the assigned area.

    + Build and maintain supportive relationships with team members through regular interactions.

    + Collaborate with operations managers, study intake, and external partners for a smooth transition of study coordination.

    + Develop and maintain Standard Operating Procedures and Work Instructions as directed by the Clinical Research Operations Manager.

    + Provide guidance, education, specialized training, and mentorship to promote team member growth.

    + Coordinate clinical research studies, including planning, organizing, and managing all related activities.

    + Support the preceptorship of new team members, monitoring their progress and maintaining open communication with the Operational Manager.

    Essential Skills

    + Experience in clinical research, particularly in oncology.

    + Proficiency in project management and clinical study coordination.

    + Knowledge of clinical trials and CRC (Clinical Research Coordinator) responsibilities.

    Additional Skills & Qualifications

    + Bachelor’s Degree in Healthcare Administration, Research, or related field with 2 years of experience in clinical research or an Associate's degree with 4 years of experience.

    + Basic Life Support (BLS) Certification.

    Work Environment

    The work environment includes a hospital setting where coordinators work closely with various clinical settings to optimize workflow and scheduling. The role offers benefits from Day One, including paid days off, a student loan repayment program, career development opportunities, and a range of wellbeing resources. Additional perks include pet insurance, debt-free education, and a nursing clinical ladder program.

    Pay and Benefits

    The pay range for this position is $90000.00 - $109000.00/yr.

     

    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*

     

    Debt-free Education* (Certifications and Degrees without out-of-pocket tuition expense)

     

    Nursing Clinical Ladder Program*

     

    Sign-on Bonus*

     

    Workplace Type

     

    This is a fully onsite position in Orlando,FL.

     

    Application Deadline

     

    This position is anticipated to close on May 23, 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.