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Clinical Research Support/Data Coordinator
2 weeks ago
Long-Term Opportunity
Competitive Pay
Requirements:
- Experience using Epic EMR
- Clinical Research experience HIGHLY preferred
- Experience with medical terminology REQUIRED
Responsibilities:
- Reads, comprehends, and follows complex study protocols for a variety of clinical research studies (early and late phase).
- Adheres to GCP and SOP guidelines of organization.
- Assists with developing and writing department workflows.
- Act as point of contact for monitors to schedule visits.
- Screen patients for initial eligibility and exclusion criteria for the clinical trials.
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 & InclusionAt 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.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email for other accommodation options.
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