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The Clinical Trial Manager (CTM) provides operational expertise and leadership to multiple clinical trial teams to ensure the effective and efficient delivery of all aspects of clinical studies across all phases. This is done in accordance with Veristat Policies, Standard Operating Procedures (SOPs), conventions, instructions, current Good Clinical Practice (GCP), International Conference on Harmonization (ICH), and local regulations.
Job Description
The CTM supports multiple clinical trial teams, overseeing study management to ensure compliance and quality throughout the study lifecycle.
What We Do
For over 30 years, Veristat has been a global leader in clinical development, supporting over 760 rare disease clinical trials and 160+ marketing applications, with 8 approvals in 2022. Learn more about our core values!
What We Offer
* Estimated salary range : £50,000 - 60,000 plus bonus, varies by region and experience.
* Benefits include remote work, flexible time off, holidays, medical insurance, tuition reimbursement, and retirement plans.
What We Look For
* Bachelor’s Degree, preferably in health sciences.
* At least 5 years' experience as a CRA in CRO or pharmaceutical settings, with project leadership skills.
* Strong knowledge of clinical operations, development processes, ICH / GCP, and regulations.
* Mentoring, coaching, and training abilities for CRAs.
* Excellent communication skills in English; additional languages a plus.
* Knowledge of therapeutic areas and clinical systems (EDC, IVRS, CTMS, eTMF).
* Proficiency in Microsoft Office and ability to learn new clinical software.
* Self-motivated, team player, capable of managing workload and priorities.
Travel up to 30% required; valid driver’s license necessary.
Veristat is an equal opportunity employer committed to diversity and inclusion.
* Seniority level : Mid-Senior level
* Employment type : Full-time
* Job function : Research, Analysis, IT
* Industry : Research Services
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