A leading global CRO, PRA is transforming clinical trials through our people, innovation and transparency. We serve clients across all phases of pharmaceutical and biotech drug development by combining therapeutic and operational expertise with local knowledge
PRA’s commitment to excellent in research begins with our people. Our workforce has grown by over 25% since 2010 and now comprises over 4,700 employees spanning more than 13 time zones and speaking more than 15 languages.
It is our philosophy that the way in which we grow our business is to focus on our employees and as such, we recognize that successful careers are found within organisations that provide the support that employees need at work, as well as the benefits they require outside the office.
Post : Senior Clinical Scientist - Oncology Women's Cancer - Home Based
Responsibilities
You will be accountable for the clinical/scientific execution of the clinical protocol as well as the scientific aspects of the implementation and conduct of a clinical trial (e.g., investigator meeting presentations, safety and medical monitoring). You may serve as the CSSM scientific representative on the clinical trial team (CTT) as well as collaborate with the Medical Writer on clinical/scientific and regulatory documents and Study manager on study deliverables. You may also be asked to provide tactical/scientific mentorship to other clinical scientists.
Candidate Profile
• Advanced degree (M.S., Ph.D., Pharm.D.) from an accredited institution in a science or health related field, or equivalent work experience required
• Bachelor’s degree in the Life Sciences highly preferred
• Clinical Scientist level = BS with 4+ years’; or MS with 3+ years’; or PhD with <2 years’ relevant career experience
• Senior Clinical Scientist level = BS with 7+ years’; or MS with 5+ years’; or PhD with <2 years’ relevant career experience
• Oncology experience required
• medical monitoring experience highly preferred
• Protocol deviation reconciliation highly preferred
• Authoring of Safety Updates (PSUR, IB, DSUR)
• Global experience highly preferred
• Pharmaceutical and/or clinical drug development experience.
• Excellent oral (including presentation) and written communication, computer/database management and project management skills
Additional Information:
Experience: 2+ years
Qualification: M.S., Ph.D., Pharm.D
Location: US - Remote
Functional Area: Oncology
Industry Type: Pharma
End Date: 30th April, 2018
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