What are the responsibilities and job description for the Senior Clinical Research Associate position at PSI CRO?
As a Senior CRA you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects rights safety and wellbeing and quality of data compliance.
OfficeBased or Homebased
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
- Supervise study activities timelines and schedules on the country level
- Be a point of contact for inhouse support services and vendors
- Be involved in quality control such as compliance monitoring and reports review
- Participate in feasibility research
- Support regulatory team in preparing documents for study submissions
Qualifications :
Additional Information :
Advance your career in clinical research and lead challenging fullservice projects on the country / regional level while growing with a rapid company that puts its people first! You will get handson involvement in every aspect of the study.
Remote Work : Employment Type :
Fulltime
Key Skills
CSS,Cloud Computing,Health Education,Actuary,Building Electrician
Vacancy : 1
About Company : PSI CRO
We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,000 driven, dedicated and passionate individuals. We work on the front-line of medical science, changing lives, and bringing new medicines to those who need them.
If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you.
