Clinical Research Associate
2 days ago
**Job Title:** Preproduction Coordinator
**Location:** eTeam
**Contract Type:** Full-time contract
**Job Summary:**
We are seeking a highly detail-oriented and organized individual to join our Operations team as a Preproduction Coordinator. The successful candidate will be responsible for ensuring the integrity of clinical trial supplies packaged at our site.
The Role
Key Responsibilities:
- Generate clinical trial packaging documentation to meet client, study, and regulatory requirements.
- Complete documentation in accordance with relevant SOPs and to comply with GMP.
- Maintain high-quality standards, ensuring all deviations are documented as required.
- Report any issues that may impact the quality or timelines specified for the packaging of supplies to your Line Manager.
- Competently perform tasks as detailed by the Preproduction skills matrix.
- Participate in the implementation of any new systems or upgrades to systems pertaining to the Preproduction department.
- Maintain a personal training record and attend training sessions as required.
- Participate in process improvement initiatives to support the Preproduction department, site, or wider organization, as appropriate.
- Stay up-to-date with industry best practices.
The Ideal Candidate
Requirements:
- English pass at Higher level or equivalent.
- Attention to detail.
- Pharma experience or education highly advantageous.
- Experience in GMP or GDP highly advantageous.
- Good IT skills.
- Proactive.
- Adaptable.
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