Sr. Clinical Project Manager, IQVIA Biotech

Posted 10 Days Ago
Be an Early Applicant
3 Locations
In-Office
93K-233K Annually
Senior level
Healthtech
The Role
Lead end-to-end planning and delivery of medium-to-large global clinical trials in cardiovascular, renal, and metabolic therapeutics. Provide strategic oversight, manage budgets, timelines, risks, and change control, liaise with sponsors, drive cross-functional teams, support business development, and mentor junior staff to ensure quality, compliance, and on-time study execution.
Summary Generated by Built In

IQVIA Biotech is seeking a Sr. Clinical Project Manager with experience in the following therapeutics: Cardiovascular, Renal, and Metabolic.

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.

Overview
The Senior Clinical Project Manager is a key leader in the delivery of clinical trials, partnering with cross-functional teams and clients to accelerate the development of life-changing therapies. This role is responsible for end-to-end clinical study execution, ensuring projects are delivered on time, within scope, and on budget, while maintaining the highest standards of quality and compliance. The Senior Clinical Project Manager provides strategic oversight, operational leadership, and serves as the primary point of contact for sponsors.

Key Responsibilities

  • Lead the planning, execution, and delivery of medium to large, multi-regional clinical studies in alignment with contractual requirements, SOPs, and regulatory standards.
  • Develop and implement integrated study management plans, ensuring consistency in processes, tools, and training.
  • Serve as the primary liaison with sponsors, building strong client relationships and ensuring transparent communication on project status, risks, and deliverables.
  • Set direction and objectives for cross-functional project teams; monitor performance and drive accountability to meet milestones.
  • Partner with Business Development on bid defenses and contribute to winning new business, including leading presentations when applicable.
  • Proactively identify, assess, and mitigate risks; lead issue resolution and implement corrective and preventative action plans.
  • Collaborate with internal functional groups to support study execution and overcome operational challenges.
  • Monitor project progress against timelines, budget, and quality metrics; provide regular updates to internal and external stakeholders.
  • Ensure financial performance by managing budgets, forecasting revenue, and identifying opportunities to accelerate delivery.
  • Manage scope changes and oversee change control processes in collaboration with stakeholders.
  • Promote continuous improvement by sharing lessons learned and best practices.
  • Mentor and support the development of junior team members and contribute feedback on team performance.

Qualifications

  • Bachelor’s Degree in Life Sciences or a related field required; advanced degree preferred.
  • Requires greater than 7 years of clinical research experience, including at least 4 years of project management experience, or an equivalent combination of education, training, and experience.
  • Proven ability to manage complex, global clinical trials and cross-functional teams.
  • Strong leadership, communication, and stakeholder management skills.
  • Demonstrated ability to manage budgets, timelines, and risk proactively.
  • Experience leading bid defenses and client engagements is preferred.

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 proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

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.

The potential base pay range for this role, when annualized, is $93,100.00 - $232,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Skills Required

  • Experience in Cardiovascular, Renal, and Metabolic therapeutics
  • Bachelor's degree in Life Sciences or related field
  • Advanced degree (MS/PhD)
  • Greater than 7 years clinical research experience
  • At least 4 years project management experience (or equivalent combination)
  • Proven ability to manage complex, global clinical trials and cross-functional teams
  • Strong leadership, communication, and stakeholder management skills
  • Demonstrated ability to manage budgets, timelines, and risk proactively
  • Experience leading bid defenses and client engagements

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.

  • 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.
  • 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.
  • 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

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The Company
Bangalore, Karnataka
61,500 Employees
Year Founded: 2016

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.

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