- 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 sites; responsible for feasibility.
- Select, coordinate and monitor activities of vendors Review of monitoring reports and conduct co-monitoring visits, as needed.
- Develop and manage trials timelines, budget and priorities.
- Participate in data review and discrepancy resolution.
- Ensure set up and maintain all systems in order to plan and implement trials and track progress.
- Generate reports to update management on conduct of trial.
- Ensure appropriate clinical trial supply plans are implemented and managed.
- Develop recruitment plans, risk-mitigation plan, monitor, and implement contingencies as required.
- Participate in monitoring study safety.
- Review key study quality metrics (e.g., eligibility, primary endpoint data, etc) and determine appropriate action in conjunction with study team.
- Assist with CRA and third party vendor training on protocols and practices.
- Lead the multi-disciplinary trials teams; include the study team meetings.
- 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.
- Working knowledge of ICH Good Clinical Practices and other relevant regulatory experience.
- Experience in executing a wide range of clinical trial activities from initiation to clinical study report.
- Strong communication skills with internal teams, sites, and vendors.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
Skills Required
- Minimum 3 years of experience in the biopharmaceutical industry or relevant clinical research
- Minimum 1 year of experience in clinical project management
- Work experience and knowledge in the oncology therapeutic area
- Bachelor's degree or relevant degree with strong emphasis on science
- Experience assisting with the conduct and management of multinational or global clinical trials
- Strong vendor management experience
- Working knowledge of ICH Good Clinical Practices and relevant regulatory requirements
- Ability to manage multiple priorities across several protocols and therapeutic areas
- Strong communication skills with internal teams, sites, and vendors
- English CV
IQVIA Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about IQVIA and has not been reviewed or approved by IQVIA.
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Healthcare Strength — Healthcare coverage is positioned as comprehensive, spanning medical/dental/vision plus programs like telemedicine, EAP resources, and additional insurance options. Feedback suggests the health offering is a meaningful part of the overall rewards package, though details can vary by location and plan design.
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Retirement Support — Retirement benefits include an employer match structure that supports employee contributions through a defined formula. This adds steady long-term value to total rewards beyond base salary.
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Leave & Time Off Breadth — Time off offerings include vacation/paid time off, holidays, and flexibility themes, with some roles described as having discretionary or unlimited time-off models. This can make the package feel more attractive even when cash compensation is viewed as only mid-range.
IQVIA Insights
What We Do
IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. IQVIA Connected Intelligence™ delivers powerful insights with speed and agility — enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. With approximately 70,000 employees, IQVIA conducts operations in more than 100 countries. To learn more, visit www.iqvia.com.
