At a Glance
- Tasks: Support global clinical studies and collaborate with cross-functional teams.
- Company: Leading biotechnology company focused on rare diseases.
- Benefits: Gain valuable experience in clinical operations and vendor management.
- Other info: Join a collaborative environment with opportunities for growth.
- Why this job: Make a real difference in patients' lives through innovative therapies.
- Qualifications: Bachelor's degree in Life Sciences or related field; experience in clinical trials.
The predicted salary is between 35000 - 45000 £ per year.
We're currently supporting an exciting opportunity with a leading rare disease biotechnology company for a Study Specialist II to join their Global Study Operations team. This role will play a key part in supporting the delivery of Phase I-IV and post-approval clinical studies, working closely with Study Managers, CROs, vendors, and cross-functional stakeholders to ensure high-quality study execution.
Key Responsibilities
- Support study planning, execution, and operational delivery activities.
- Contribute to site feasibility, site management, and investigator support.
- Oversee essential study documentation and Trial Master File (TMF) management.
- Support vendor oversight and management, including CROs and specialist vendors.
- Coordinate regulatory document collection and study start-up activities.
- Assist with investigator meetings, site training materials, and study communications.
- Manage study tracking, payments, document workflows, and operational processes.
- Support risk identification and mitigation activities across assigned studies.
- Act as a key operational partner within cross-functional study execution teams.
What We're Looking For
- Bachelor's degree in Life Sciences, Health Sciences, Nursing, or a related field (or equivalent industry experience).
- Experience supporting global clinical trials within a pharmaceutical, biotechnology, or CRO environment.
- Knowledge of clinical study operations, site management, and study execution.
- Experience working with external vendors such as CROs, central labs, or imaging providers.
- Strong understanding of GCP, compliance, and clinical trial processes.
- Excellent organisational, communication, and stakeholder management skills.
Why Apply?
- Join a company dedicated to developing therapies for patients with rare genetic diseases.
- Work within a highly collaborative global clinical operations environment.
- Gain exposure across study management, vendor oversight, and global clinical trial delivery.
- Opportunity to contribute to studies that have a meaningful impact on patients' lives.
Interested? Apply now or message me directly for more information.
Study Specialist II – Global Study Operations in England employer: Skills Alliance
Join a leading biotechnology company that is committed to making a difference in the lives of patients with rare genetic diseases. With a strong focus on collaboration and innovation, this role offers you the chance to work within a dynamic global clinical operations team, providing ample opportunities for professional growth and development. Enjoy a supportive work culture that values your contributions and fosters meaningful engagement in impactful clinical studies.
