Clinical Trials Coordinator
4 weeks ago
Clinical Trials Specialist
Job Summary:
Actalent is seeking a highly skilled Clinical Trials Specialist to join our team. As a Clinical Trials Specialist, you will play a critical role in the initiation, activation, and ongoing management of clinical trials.
Key Responsibilities:
- Collaborate with various departments to prepare and review study tools, verify necessary approvals, and translate finalized protocol treatment plans.
- Ensure timely prescreening of potential subjects, obtain informed consent, and provide backup support for patient registration.
- Manage protocol-specific orders, coordinate patient care, and ensure accurate documentation.
- Grade adverse events, complete Serious Adverse Event forms, and support monitoring visits and audits.
- Maintain high standards of professional responsibility and performance, while staying current with continuing education and regulatory requirements.
Requirements:
- 2-3 years clinical research coordination experience
- 1 year oncology required
- Bachelor's degree
- Experience with Oncore Study-start up task list
- Experience in handling Case Report Forms (CRF) and database queries
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. We are committed to creating an inclusive environment through persistent self-reflection, building a culture of care, engagement, and recognition with clear outcomes, and 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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