
Senior Life Sciences Professional
5 days ago
We are seeking a seasoned professional to join our team as a Senior Clinical Research Associate.
This role will involve overseeing all aspects of clinical trials, ensuring they are conducted in accordance with applicable SOPs, regulations and ICH guidelines.
The successful candidate will be responsible for monitoring clinical trials, conducting site qualification visits, supporting feasibility and site selection activities, negotiating site contracts and managing study site data.
Key qualifications for this role include an undergraduate degree in Life Sciences, at least 3-4 years' experience in monitoring clinical trials and experience in EDC & CTMS systems.
A strong understanding of ICH-GCP requirements and willingness to travel are also essential.
As a member of our team, you will contribute towards efficient trial management and collaborate with project teams to achieve shared goals.
- Key Responsibilities:
- Monitor clinical trials and ensure compliance with relevant SOPs, regulations and ICH guidelines
- Conduct site qualification visits and support feasibility and site selection activities
- Negotiate site contracts and manage study site data
- Collaborate with project teams to achieve shared goals and contribute to efficient trial management
Requirements:
- Undergraduate degree in Life Sciences (e.g. Biology, Chemistry, Pharmaceuticals)
- At least 3-4 years' experience in monitoring clinical trials in CRO, Pharmaceutical and/or Biotechnology industries
- Experience in EDC & CTMS systems
- Strong understanding of ICH-GCP requirements
- Willingness to travel
About the Role:
This is an exciting opportunity to join a dynamic team and contribute to the delivery of high-quality clinical trials.
If you are a motivated and experienced professional looking for a new challenge, we encourage you to apply.
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