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RESPONSIBILITIES In order of importance, indicate the primary responsibilities critical to the performance of the role. It is recommended not to list actual tasks but focus on 5-8 essential responsibilities
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at the center of our operations and you'll find that everything we do, every day, is in line with an unwavering commitment to quality. The primary purpose of this job role is to function as a member of the
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-budget execution of protocols Interact with regulatory authorities, key opinion leaders, and principal investigators. Leads Clinical Regulatory Authority interactions, accountable for providing responses
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Maintain rigorous records of experimental progress using electronic laboratory notebooks Qualifications Must-Have Bachelor's Degree and 6+ years of experience or Master's degree and 4+ years of experience
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recommendations Demonstrated ability to manage vendors to ensure effective project delivery Nice-to-Have Master's degree Experience in quality control and/or quality assurance within the pharmaceutical industry
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ROLE SUMMARY The Clinical Research Physician will act as an Investigator and/or Principal Investigator for clinical trials conducted in the PCRU and has responsibilities and accountabilities
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to achieve new milestones and help patients across the globe. How You Will Achieve It Indicate the primary responsibilities critical to the job. Executes clinical research studies in accordance with
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operational expertise to ensure creativity, excellence, and integrity in clinical development. The CL also serves as principal contact on medical and safety issues for all study execution lines, study managers
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. Qualifications Must-Have Bachelor's Degree (Science/Chemistry-Biology) with 3 to 5 years of experience or master's degree (Science/Chemistry-Biology) with 0 to 3 years of experience Experience with laboratory data
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to achieve new milestones and help patients across the globe. How You Will Achieve It Indicate the primary responsibilities critical to the job. Executes clinical research studies in accordance with