Lead Global Clinical Trials Manager (Oncology)

IQVIA LLC; Reading; On-site; GBP 65,000 - 90,000; Full time

Job summary

IQVIA LLC in Reading, Berkshire, United Kingdom, is seeking an experienced Clinical Trial Manager to lead multicenter trials from initiation to study report. You will coordinate cross-functional teams, manage timelines and budgets, and ensure compliance with ICH-GCP and regulatory standards.

The role requires at least 4 years in biopharma and global clinical project management experience, with oncology focus.

Qualifications

• Minimum of 4 years' experience in the biopharmaceutical industry.
• Minimum 3 year or experience in Clinical Project Management at global level.
• Proven work experience and knowledge of Oncology therapeutic area.
• Bachelor's Degree or relevant degree with strong emphasis on Science.
• Ability to effectively manage multiple priorities across several protocols and therapeutic areas simultaneously.
• Strong experience in vendor management.

Responsibilities

• Accountable to deliver trials on time, within budget, and with highest achievable quality.
• Assist in review, development and writing of clinical trial documents and manuals, including but not limited to Protocol, Case Report Forms, informed consent forms, Clinical Study Report and other regulatory documents.
• Lead the evaluation and selection of investigative, clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
• Collaborate with internal stakeholders and vendors to improve trial delivery.

Skills

Vendor management

ICH-GCP knowledge

Communication skills

Clinical trial management

Oncology knowledge

Global PM experience

Regulatory knowledge

Education

Science degree

Job description

IQVIA LLC in Reading, Berkshire, United Kingdom, is seeking an experienced Clinical Trial Manager to lead multicenter trials from initiation to study report. You will coordinate cross-functional teams, manage timelines and budgets, and ensure compliance with ICH-GCP and regulatory standards.

The role requires at least 4 years in biopharma and global clinical project management experience, with oncology focus.