| Clinical Trials Assistant |
| Please Quote Reference Number 15295 |
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Bachelor’s degree in health sciences or a health-related discipline required
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Permanent Full Time role 32-40 hours per week
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Gain hands-on experience with clinical trial operations
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Position Summary:
Silverdale Medical is seeking a motivated and detail-oriented postgraduate student to work full-time, supporting the implementation and management of clinical trials as part of the PCRN network. The successful candidate will assist in the safe and effective execution of clinical trial protocols, ensuring compliance with all regulatory requirements, including the protocol, standard operating procedures (SOPs), and ICH-GCP guidelines. This is an excellent opportunity to gain hands-on experience with clinical trial operations and contribute to meaningful health research.
Key Responsibilities:- Assist with the safe and effective implementation of clinical trial protocols.
- Ensure trial procedures are conducted, documented, and reported in accordance with ICH-GCP, SOPs, and regulatory requirements.
- Participate in the recruitment and coordination of trial participants.
- Perform accurate data entry of trial data into designated systems.
- Assist with the review and verification of trial documentation for completeness and compliance.
- Support invoicing for completed elements of the trial protocol.
- Attend and contribute to team meetings and discussions regarding the trial progress.
Qualifications and Experience:- Bachelor's degree in health sciences or a health-related discipline required.
- Enrolled in or pursuing a Master's or PhD in a relevant field (advantageous).
- Understanding of clinical research processes and regulatory guidelines (advantageous but not required).
- Strong organisational skills and attention to detail.
- Ability to work collaboratively as part of a research team.
- Career aspiration to pursue scientific research preferred.
- Strong communication skills, both written and verbal.
- Familiarity with data entry, invoicing, and administrative tasks is an asset.
Benefits:- Gain valuable experience in clinical trial management and operations.
- Opportunity to develop skills and knowledge in regulatory compliance and research protocols.
Hours and Location:- Full-time during business hours 32-40 hours per week ,
- In person attendance at workplace required.
- Silverdale Medical 7 Polarity Rise Silverdale
APPLY NOW with an up to date CV and Cover Letter.
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| Please Quote Reference Number 15295 |
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