Clinical Project Associate

3 weeks ago

West London, United Kingdom ISR Recruitment Full time

**Hybrid-working (2 days onsite, 3 days WFH)**:

- **Stockley Park, Uxbridge**:

- **12 month contract**:

- **c£18 to £22 per hour (via PAYE/Umbrella)**

**The Opportunity**:
To join a global pharma leader working as a Clinical Project Administrator on an initial 12 month contract providing administrative and coordination support for a number of high-profile Virology projects.

Full training will be provided on internal systems that will allow you to build knowledge and become an integral team-player, allowing you the time to learn the required skills to manage multiple stakeholders with ongoing operational support.

**Skills and Experience**:
To be considered for this position you will require a minimum of 12 months on-site clinical trial monitoring experience in a commercial CRO or sponsor environment, or with applicable clinical research regulatory requirements, i.e. GCP and ICH guidelines.
- BSc in a relevant scientific discipline preferred
- Prior experience at CPA level would be useful but not a must
- Knowledge of MHRA and or EU Regulations, ICH Guidelines, GCP, and/or familiarity with standard clinical operating procedures is a plus
- Must be familiar with Word, PowerPoint and Excel
- Excellent verbal and written communication skills and interpersonal skills are required.
- Must be able to work both independently and as part of a team

**Role and Responsibilities**:

- Provides administrative assistance in study implementation and the ongoing coordination, either directly or via CROs
- Tracking and preparing study-specific information utilizing databases, spreadsheets, and other tools
- Working with the different members of the study management team as necessary to resolve study related administrative tasks
- Printing and coding of study documentation for the Trial Mater File system (TMF), and/or upload of documents to the Veeva eTMF system
- Completion of transmittal forms when necessary and filing of documentation into the TMF according to the client’s SOPs
- Performing detailed TMF reviews according to the client’s SOPs and processes
- Under close supervision reviews and participates in the quality assurance of data or documents
- Any other tasks as delegated by the study team.

**Applications**:
**Please call Edward Liang here at ISR Recruitment on 07436 071 872 to learn more?

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