Senior Clinical Trial Management Associate

3 weeks ago

Uxbridge, United Kingdom Hobson Prior Full time

Hobson Prior are currently looking for a Senior Clinical Trial Management Associate to join a brilliant biotech establishment on a contract basis. Our client is focused on producing a healthier world.

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 internal clinical operations and medical affairs databases and clinical study data and document repositories.
- Support in planning safety, interim and final study documents, which involves solving data inconsistencies.
- You will execute working procedures to promote high quality, effective, and compliant systems for late phase research management.
- Assist the CO LP study lead as a crucial operational contact with external investigators, internal shareholders and designated CROs.
- Offer administrative support in site selection, study execution and current arrangement of study sites, either directly or through CROs.
- Any other assigned duties.

**Key Skills**:

- Able to prioritise various tasks simultaneously and complete objectives.
- Capable of learning with a flexibility to uphold a fast pace.
- Interpersonal, presentation and communication skills both verbally and in writing.
- A tenacious individual who demonstrates perseverance.
- Customer focused.
- An organised individual who is able to plan and manage time efficiently.
- Administrative capabilities.

**Requirements**:

- Educated to a degree level in a pertinent scientific field with pertinent clinical experience within a pharmaceutical or healthcare organisation.
- Exhibits the company's core values of teamwork and the ability to prioritise workload and deliver brilliant outcomes.
- Able to uphold both internal/external networking and cross-functional collaboration.
- Exhibits a high sense of urgency and commitment to brilliance in the successful implementation of deliverables.
- Expertise and comprehension of ICH GCP, FDA and EMEA guidelines and regulations suitable for post-authorisation studies.
- Acquaintance with regular medical/scientific vocabulary.
- Capable of contributing to either divisional or interdivisional tactical initiative under supervision.
- Ability to participate in SOP development when needed.

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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