Description
Responsibilities:- Closely interact with the Translational Research and Biomarker groups to design and implement biomarker strategies for science-driven clinical programs
- Create and implement clinical development plans with a focus on early clinical development
- Design, execute and complete Phase 1a, Phase 1b and/or Phase 2 trials
- Select, qualify and maintain excellent relationships with clinical investigators
- Contribute to the selection and oversight of CROs
- Contribute to the authoring and review of regulatory documents (Annual Report, Investigator Brochure, responses to information requests, etc.)
- Develop and maintain relationships with outside experts as needed to achieve clinical development goals
Requirements:
- MD (or non-US equivalent)
- Board eligible/certified (or non-US equivalent)
- Minimum of 4 years of related clinical experience, minimum of 2 years of biotech/pharmaceutical industry experience
- Oncology training strongly preferred
- Ability to design and implement clinical development plan
- Excellent verbal and written communication skills
- Strong organizational skills
To find out more about Real please visit www.realstaffing.com