Clinical Research Scientist responsible for assisting Clinical Research Physician with project team members, preparing documents, and overseeing study implementation. Must have degree in Life Sciences, minimum 2 yrs experience in medical or technical writing, and excellent communication skills.
Requirements
- Degree in Life Sciences
- Minimum 2 yrs experience in medical or technical writing
- Clinical monitoring experience preferred
- Excellent written and verbal communication skills and interpersonal skills
- Extensive medical/scientific and clinical research knowledge
- Knowledge of Medical Terminology
- Knowledge of clinical trial design, basic statistics, pharmacodynamics and pharmacokinetics
- Proficient at data interpretation
- Experience in protocol development, study report preparation, Investigator Brochure preparation, regulatory submissions
- Experience in all aspects of the drug development process
- Knowledge of GCP and ICH Guidelines
- Experience in presenting at Investigator Meetings
- Detail-oriented, well-organized
- Ability to assimilate technical and scientific information quickly
- Clinical project management skills
- Proficient in Microsoft Word, Excel, PowerPoint; Microsoft project a plus
- Demonstrated ability to work as part of a team
- High level of interpersonal and communication skills (written and verbal)