A commercializing biotech which is rapidly expanding its early phase studies is seeking an experienced Clinical Scientist who will provide scientific, pharmacologic and/or medical input into publications, trial designs and protocols across all stages of clinical development and support regulatory submissions worldwide. This person will work with cross-functional teams and global collaborations to integrate broad medical and scientific input into assigned development programs. This individual will work with clinical research, translational, program management, regulatory and operational staff (among others) to develop and implement protocols, publications, presentations and submissions that advance clinical development plans for assigned programs and molecules.
This role will work with cross-functional and global collaborations to integrate broad medical and scientific input into development programs and clinical development plans for assigned programs and molecules. Depending on corporate/programmatic needs and individual aptitudes, the role may primarily focus on Safety, Clinical or Scientific Research aspects of assigned programs. It is intended that the Clinical Scientist will develop into a leadership role and will offer excellent prospects for progression.
Required Knowledge, Skills & Abilities:
At least 5-7 years clinical research experience in the pharmaceutical industry or CRO
PhD/PharmD/RN/DO or the equivalent preferred.
Oncology experience required;
Working knowledge of clinical trial design and execution;
Experience in protocol development and regulatory submissions;
Adherence to the highest standards for trial conduct, patient safety and data integrity;
Medical/technical writing and basis statistics expertise preferred;
Working knowledge of GCP, ICH Guidelines and standard medical terminology
For more information on this role, the company and the excellent compensation scheme please CLICK APPLY and forward an up-to-date resume.
Salary: $180,000 - $220,000 Per annum
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