My client is seeking an experienced Clinical Project Assistant who will provide support to the global trial managers within the EMEA region.

Role

Providing support across several studies, including involvement from study start-up through study close-out activities, and will work with the CRO to execute the study to agreed timelines and budget.

Essential Duties and Job Functions:
* Provide administrative assistance in study implementation and the ongoing coordination

* Tracking and preparing study-specific information

* 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 TMF, and/or upload of documents to the Veeva eTMF system.

* Completion of transmittal forms

* Performing detailed reviews according to SOPs and processes.

* Supervision reviews and participates in the quality assurance of data or documents

* Drafts meeting agendas and prepares meeting minutes

Knowledge, Experience & Skills:

* BSc in a relevant scientific discipline preferred but not required.

* Excellent verbal and written communication skills and interpersonal skills are required.

* Knowledge of FDA and or EU Regulations, ICH Guidelines, GCP, and/or familiarity with standard clinical operating procedures is a plus.

* Prior CPA experience preferred.

Parkside Recruitment Ltd is acting as an Employment Business in relation to this vacancy. Parkside Recruitment is an Equal Opportunities Employer.