Oncology Clinical Trial Operations Lead

IQVIA LLC; Reading; On-site; GBP 70,000 - 100,000; Full time

Job summary

IQVIA is recruiting for a Clinical Operations Lead to support sponsor-dedicated Clinical FSP activities and manage trial timelines, vendor relationships, and site coordination.

Minimum 3 years in biopharmaceutical/clinical research, 1+ year in clinical project management, and strong oncology experience are required. A science-focused degree and excellent communication are essential for success at IQVIA.

Qualifications

• Minimum of 3 years’ experience in the biopharmaceutical industry or other relevant clinical research experience.
• Minimum 1 year or experience in Clinical Project Management.
• Proven work experience and knowledge of Oncology therapeutic area.
• Bachelor’s Degree or relevant degree with strong emphasis on Science.
• Prior experience in assisting the conduct and management of multinational/ global clinical trials.
• Strong experience in vendor management.
• Working knowledge of ICH Good Clinical Practices and other relevant regulatory experience.
• Ability to effectively manage multiple priorities across several protocols and therapeutic areas simultaneously.
• Strong communication skills with internal teams, sites, and vendors.

Responsibilities

• Assist in the review, development and writing of clinical trial documents and manuals, including but not limited to study manuals, laboratory or biomarker plans.
• Create Master ICF template and review site changes.
• Update template for new risks and new amendments information.
• Participate in the feasibility and evaluation of investigative sites.
• Assist in the development and management of study timelines and priorities, including recruitment tools/ strategy and patient retentions plan.
• Plan and organize meetings with team support (eg. investigator/ coordinator meetings).
• Assist in the development of the IP and co-medication strategy.
• Monitor study specific timelines and key deliverables; focus on management of vendors (eg. Monitoring, Sample management, IVRS, Laboratory).
• Develop relationships with investigational sites and institutions to enhance conduct of the trial.
• Acts as preliminary liaison for study sites to convey trial information, answer questions and in accordance with the escalation pathway.

Skills

Clinical project management

Oncology

Vendor management

ICH-GCP knowledge

Multinational trials

Science degree

Strong communication

Biopharmaceutical industry experience

Education

Bachelor’s Degree in Science

Job description

IQVIA is recruiting for a Clinical Operations Lead to support sponsor-dedicated Clinical FSP activities and manage trial timelines, vendor relationships, and site coordination.

Minimum 3 years in biopharmaceutical/clinical research, 1+ year in clinical project management, and strong oncology experience are required. A science-focused degree and excellent communication are essential for success at IQVIA.