Actalent • Philadelphia, PA 19133
Job #2694387423
Recruit, Screen, Enroll subjects in to clinical trails
Explain Informed Consent process
Document adverse events
Collect study documents, protocols, regulatory documents, informed consents, case report forms and source documents
Prepare the Institutional Review Board, IRB applications
Additional Skills & Qualifications:
BA/BS preferred
Experience with in-hospital clinical research
1- 3 years clinical research experience required
Experience with adverse event reporting
Experience with patient recruitment and consenting
Effective communication and writing skills
Knowledge of IRB and human research protection regulations
PAY RANGE (dependent on relevant experience): $55k - $62k
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.
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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