Clinical Research Coordinator

3 weeks ago


Orlando, Florida, United States Actalent Full time

Job Title:
Clinical Research Coordinator


The Clinical Research Coordinator, under limited supervision, plans, coordinates, evaluates, and performs the care of participants and collects data for assigned research projects.


The CRC-II (Non-RN) follows study-specific protocol guidelines, communicates with Principal Investigators (PI), Sub-Investigators (Sub-I), Clinical Research Lead, and clinical research support staff.


The CRC advocates for the patient while adhering to industry-sponsored and investigator-initiated clinical trials in accordance with trial protocols, FDA regulations, and ICH/GCP guidelines.


Requirements:

  • 1+ years oncology experience
  • Bachelors Degree (required)
  • 2+ years of clinical research experience


Soft Skills:

  • Positive interpersonal communication skills
  • Effective communication with healthcare team
  • Patient advocacy
  • Independent work
  • Timely documentation


Environment:

This is a fully on-site position in Orlando, Florida.


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.


Diversity, Equity & Inclusion:

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people.


DE&I are embedded into our culture through:

  • Hiring diverse talent
  • Maintaining an inclusive environment through persistent self-reflection
  • Building a culture of care, engagement, and recognition with clear outcomes
  • Ensuring growth opportunities for our people


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.



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