At a Glance
- Tasks: Support clinical trials by managing timelines, documents, and vendor relationships.
- Company: Leading biopharma company focused on innovative clinical research.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Dynamic role with exposure to multinational trials and strong career advancement potential.
- Why this job: Make a global impact in healthcare by influencing trial execution and quality.
- Qualifications: 3+ years in biopharma, 1+ year in Clinical Project Management, and oncology experience.
The predicted salary is between 40500 - 49500 £ per year.
Overview
In this role you will support the Clinical Trial Operational team to execute trials across therapeutic areas.
You will liaise with CROs and vendors to ensure study timelines and deliverables are met.
You’ll help develop trial documents, timelines, feasibility assessments, and site relationships, driving smooth operation and risk management.
The position offers exposure to multinational trials and collaboration with a key client within a sponsor-dedicated Clinical FSP.
This is a chance to influence trial execution and quality in a global context.
Responsibilities
- Review, develop and write clinical trial documents and manuals (e. g., study manuals, biomarker plans)
- Create and update Master ICF templates, track site changes and amendments
- Assess investigative sites feasibility and evaluative input
- Develop and manage study timelines, recruitment strategy, and patient retention plans
- Plan team meetings with investigators and coordinators
- Contribute to IP and co-medication strategy
- Monitor timelines and vendor deliverables (e. g., Monitoring, Sample management, IVRS, Laboratory)
- Foster relationships with investigational sites to improve trial conduct
- Serve as preliminary liaison to sites, communicating trial information and escalation as needed
- Key requirements
- Minimum 3 years in biopharma or related clinical research
- Minimum 1 year in Clinical Project Management
- Proven experience in Oncology
- Bachelor’s Degree or relevant science-focused degree
- Experience conducting multinational/global trials
- Strong vendor management experience
- Working knowledge of ICH GCP and regulatory requirements
- Ability to manage multiple priorities across protocols and therapeutic areas
- Strong communication with internal teams, sites, and vendors
- strong communication skills
- multi-tasking and prioritization
- stakeholder management
- vendor management
- clinical trial project management
- regulatory knowledge (ICH GCP)
Clinical Trial Manager in Reading employer: IQVIA
At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that prioritises innovation and employee well-being. Our South West England location provides flexible working arrangements, comprehensive well-being support, and robust career development opportunities through our AI-powered talent marketplace, ensuring that you can thrive both personally and professionally while contributing to meaningful advancements in healthcare.
