Clinical Trial Administrator

5 days ago

Bengaluru, India PSI CRO Full time

Company Description

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 2700 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.

**Job Description**:
Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information.

Office Based in Bangalore

You will:

- Assist project teams with selective aspects of trial management from start-up to close-out on a country level
- Work closely with site-monitors and interface with site representatives, vendors and PSI project teams
- Be responsible for document management and maintenance of the Trial Master File for your sites and projects
- Update and maintain (automated) tracking systems and schedules
- Coordinate various activities within clinical research projects
- Provide support for administrative tasks, e.g. meeting coordination, agenda and minute preparation on a project level

**Qualifications**:

- College/University degree or an equivalent combination of education, training & experience
- Prior experience in Clinical Research / CRO environment
- Administrative work experience, preferably in an international setting
- Prior experience with site routine monitoring is a plus
- Full working proficiency in English
- Ability to plan, multitask and work in a dynamic team environment
- Communication and collaboration skills

Additional Information

This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.

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