Job Description
Responsibilities
- Designing, planning, coordinating, and conducting clinical research studies
- Acting as the primary contact for assigned study site personnel
- Performing site assessments and qualification visits
- Developing and managing key study site documentation
- Overseeing CROs for site management activities
- Executing site management activities for studies across all phases
Requirements
- Bachelor’s degree in Science, preferably in Health Sciences or engineering
- Working experience in the Medical Device or Diagnostics industry
- Experience in clinical study of IVD/Medical Device/Drug
- Experience in cardiovascular/metabolic indications and Near Patient Care or Point of Care
- Knowledge of ICH GCP guidelines
- Ability to analyze and solve problems
- Flexibility to work in a fast-paced environment
ATS Optimization Keywords
Below are skills and terms extracted directly from this job posting to improve Applicant Tracking System (ATS) visibility. This content is included as a reference for candidates to tailor their applications.
Hard Skills
- clinical research
- site assessments
- study site documentation
- site management activities
- clinical study
- IVD
- medical device
- drug development
- cardiovascular indications
- metabolic indications
Soft Skills
- problem analysis
- flexibility
- coordination
- communication
Certifications & Qualifications
- Bachelor’s degree in Science
- Bachelor’s degree in Health Sciences
- Bachelor’s degree in engineering