At a Glance
- Tasks: Manage site activation for clinical studies and ensure compliance with regulations.
- Company: Join a leading Pharma Client in a collaborative remote environment.
- Benefits: Work remotely, gain valuable experience, and enhance your career in clinical research.
- Other info: Fast-paced role with opportunities for professional growth and development.
- Why this job: Make a real impact in clinical trials while working with a dynamic team.
- Qualifications: Bachelor's in Life Sciences and 3 years of clinical research experience required.
The predicted salary is between 45000 - 55000 £ per year.
Join a leading Pharma Client as a
Senior Site Activation Specialist!
Job Overview
We are seeking an experienced Senior Site Activation Specialist to support clinical studies from site selection through site activation and startup activities.
You will play a key role in managing regulatory, ethics, and contractual submissions while ensuring compliance with ICH-GCP guidelines, local regulations, study requirements, and project timelines.
This is an excellent opportunity to work remotely within a fast-paced and collaborative clinical research environment.
- Location: Remote
- Contract Length: Until 21 December 2026
- Start Date: ASAP
Key Responsibilities
- Act as the primary point of contact (SPOC) for investigative sites, Site Activation Managers, project teams, and key stakeholders.
- Coordinate and execute site startup and activation activities in line with study timelines, SOPs, and regulatory requirements.
- Prepare, review, and manage site regulatory documentation, ensuring compliance, accuracy, and completeness.
- Support regulatory and ethics submissions, including informed consent form (ICF) adaptations and responses to authority queries.
- Conduct quality control reviews of regulatory documents, investigator documentation, and submission packages.
- Track approvals, submissions, document execution, and site activation milestones to ensure timely study startup.
- Maintain accurate records within CTMS, TMF, e TMF, and clinical study startup tracking systems.
- Key Requirements
- Bachelor's Degree in Life Sciences or a related discipline.
- Minimum 3 years' clinical research experience with a focus on study startup, site activation, or clinical operations.
- Strong knowledge of clinical trial startup processes, regulatory requirements, ethics submissions, and ICH-GCP guidelines.
- Experience working within CRO and/or Sponsor environments.
- Hands-on experience with CTMS, TMF/e TMF, and study startup tracking systems.
- Excellent organisational, communication, stakeholder management, and problem-solving skills.
- Additional Information
- Interview Process: 1-Stage
How to Apply If you're interested in this role, click
'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.
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Senior Site Activation Specialist in London employer: Hays Specialist Recruitment Limited Careers
Hays Education is an exceptional employer, offering a supportive and collaborative work environment for SEN SLD/PMLD teachers in the Hounslow/Hillingdon area. With access to exclusive vacancies, ongoing professional development, and a dedicated consultant to guide your career, you will find ample opportunities for growth while making a meaningful impact on the lives of pupils with special educational needs. Join us to be part of a community that values inclusivity and fosters both personal and professional development.
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