We are looking for a temporary freelancer Clinical Research Associate to work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications.
Only CVs in English will be considered
Home-based position in Peru
You will:
- Conduct and report all types of onsite monitoring visits
- Be involved in study startup (if applicable)
- Perform CRF review, source document verification and query resolution
- Be responsible for site communication and management
- Be a point of contact for in-house support services and vendors
- Communicate with internal project teams regarding study progress
- Participate in feasibility research
- Support regulatory team in preparing documents for study submissions
- College/University degree in Life Sciences or an equivalent combination of education, training & experience
- Independent on-site monitoring experience in Peru
- Experience in all types of monitoring visits in Phase II and/or III
- Availability to travel
- Full working proficiency in English and Spanish
- PC skills to be able to work with MS Word, Excel and PowerPoint
- Ability to plan, deal with different tasks and work in a dynamic team environment
- Communication, collaboration, and problem-solving skills
Become a full-fledged clinical research professional with the support of a knowledgeable and professional team. You will develop a variety of skills while progressing with the company and contributing to our full-scale challenging projects.
