Clinical Trial Administrator

1 week ago

London, United Kingdom Hobson Prior Full time

Hobson Prior are looking for a Clinical Trial Administrator to join a brilliant pharmaceutical organisation on a contract basis located in Holborn. Our client is focused on producing novel remedies that meet global needs.

Please note that to be considered for this role you must have the right to work in this location.

**Key Responsibilities**:

- For this role, you will uphold and update any electronic study folders to guarantee eFiles ponder any paper TMF/OSF and contrarywise.
- Conduct/supervise periodic QC of OSFs and/or TMFs at the company to guarantee completeness and precision.
- Support the ethics proposals as well as keep track of proposals and sanctions for the study.
- Mediate with regulatory affairs to warrant connection with regulatory sanctions.
- You will produce and uphold study contact lists and pertinent information databases for study teams.
- Enable and track any study payments adhering to the internal sanction procedure.
- Warrant learning and knowledge transfer throughout and at the accomplishment of the clinical study(s).
- Partake in the development and upkeep of the company's SOPs and guarantee participation to the process development in the clinical operations team and the company in general.
- Any other assigned duties.

**Key Skills**:

- Agile with the ability to manage various tasks simultaneously to meet deadlines while delivering high quality work within an energetic setting.
- Outcomes driven outlook with a sense of urgency.
- Capable of contributing to and acknowledging problems and demands.
- Ability to engage efficiently with all levels in the company, as well as with associates and partners on an external level.
- Able to work independently while under mínimal supervision.
- Willing to get involves with a can-do mindset.
- Familiarity working within a team setting while under pressure.
- A diplomatic and strategic individual with the ability to mediate with personnel and management.
- A meticulous individual with a high attention to detail.
- Communication skills both verbally and in writing with the ability to manage time efficiently.

**Requirements**:

- Educated to a degree level in a health science, nursing, pharmacy or similar discipline.
- Familiarity in a CTA role and/or document manager role within a clinical research or pharmaceutical organisation.
- Know-how of pharmaceutical industry/clinical trial procedure, preferably early phase.
- Acquaintance, knowledge and execution of eTMFs.
- Prior involvement with bringing in new electronic systems.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

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