Clinical Trial Administrator

4 weeks ago

Bengaluru Karnataka, 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.

Join our international team and be the key support to clinical research projects, streamlining communication within a clinical project team, supporting monitors and site management associates, maintaining systems, managing documents & information.

Office Based in Bangalore

You will:

- Assist clinical project teams with selective aspects of trial management from start-up to close-out on a country level.
- Ensure that the clinical project team is timely supplied with study information and documents.
- Work closely with site monitors and interface with site representatives, and vendors.
- Coordinate information flow on clinical supplies inventory, storage, and reconciliation within the project team.
- Be responsible for document management and maintenance of the Trial Master File for sites and projects.
- Update and maintain (automated) tracking systems and schedules.
- Ensure completeness and consistency of information in study-specific and corporate tracking systems.
- Coordinate various activities within clinical research projects (support with regulatory and ethics committee submissions and notifications, assistance with financial tasks, preparations to audits and inspections, translations and review of non-medical documents).
- Support organization of internal team meetings, including preparation of agenda and minutes.
- Tracks initial and ongoing project team training, ensure appropriate access is provided to new project team members.

**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
- 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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