IQVIA

Sr. Clinical Project Manager

IQVIA • $93K — $232K *
Washington, DC 20011In-Person
Pharmaceuticals & Biotech
5 - 7 years of experience
Today
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Job Overview by Ladders

Qualifications

  • Bachelor's degree in Life Sciences, Nursing, Biomedical Engineering, Public Health, or related field.
  • Minimum of 7 years in clinical research, with 4 years in clinical project management.
  • Experience in MedTech, medical devices, CROs, biotechnology, or pharmaceutical industries.
  • Proven track record in managing global and multi-country clinical studies.
  • Strong knowledge of ICH-GCP, ISO 14155, and FDA regulations.

Responsibilities

  • Lead planning and execution of global MedTech clinical studies.
  • Maintain strong client relationships as the primary project contact.
  • Develop and manage study timelines, budgets, and risk management plans.
  • Ensure project milestones and study objectives are met through team leadership.
  • Monitor and resolve project risks and issues throughout the study.
  • Ensure compliance with regulatory and quality standards.
  • Collaborate with various functional teams for study execution excellence.

Benefits

  • Comprehensive health and welfare benefits.
  • Opportunities for professional development and mentoring.
  • Involvement in bid defenses and new business opportunities.
  • Encouragement of continuous process improvement and operational excellence.
Full Job Description
Job Summary

The Senior Clinical Project Manager is responsible for leading the planning, execution, and delivery of global MedTech clinical studies supporting the development and commercialization of medical devices. This individual serves as the primary point of contact for sponsors and cross-functional teams, ensuring studies are delivered on time, within budget, and in compliance with applicable regulatory and quality requirements.

The Senior Clinical Project Manager provides strategic leadership across multi-country clinical programs, driving operational excellence, customer satisfaction, and successful study outcomes.

Job Responsibilities
  • Lead the planning, execution, and delivery of global and multi-country MedTech clinical studies.
  • Serve as the primary project contact for sponsors and maintain strong client relationships throughout the study lifecycle.
  • Develop and manage study timelines, budgets, forecasts, risk management plans, and project deliverables.
  • Lead cross-functional project teams to ensure milestones are achieved and study objectives are met.
  • Monitor study progress and proactively identify, escalate, and resolve project risks and issues.
  • Ensure compliance with ICH-GCP, ISO 14155, applicable regulatory requirements, SOPs, and quality standards.
  • Collaborate with Clinical Operations, Data Management, Biostatistics, Regulatory Affairs, Safety, and other functional groups to support successful study execution.
  • Manage study finances, including forecasting, scope management, change orders, and overall project profitability.
  • Support bid defenses and business development activities for new opportunities.
  • Drive continuous process improvement and share lessons learned and best practices across project teams.
  • Mentor and support the development of junior project management and clinical operations staff.
  • Provide regular project updates and strategic recommendations to sponsors and internal stakeholders.


Job Qualifications

Education
  • Bachelor's degree in Life Sciences, Nursing, Biomedical Engineering, Public Health, Healthcare, or a related scientific discipline required.

Experience
  • Minimum of 7 years of clinical research experience, including at least 4 years of clinical project management experience.
  • Experience managing clinical studies within the MedTech, medical device, diagnostics, CRO, biotechnology, pharmaceutical, or healthcare industries.
  • Demonstrated experience leading global and multi-country clinical studies across North America, Europe, Asia-Pacific, and other regions.
  • Experience managing cross-functional project teams and complex stakeholder relationships.
  • Experience supporting studies intended for regulatory submissions, product development, and post-market evidence generation preferred.

Knowledge, Skills & Abilities
  • Strong knowledge of clinical trial management and applicable regulations, including ICH-GCP, ISO 14155, FDA, and global regulatory requirements.
  • Proven ability to lead global, cross-functional teams in a matrix environment.
  • Excellent client relationship management, communication, presentation, and negotiation skills.
  • Strong project planning, organizational, and problem-solving abilities.
  • Demonstrated experience managing project budgets, contracts, forecasting, and financial performance.
  • Ability to manage multiple priorities and deliver results in a fast-paced environment.
  • Strong attention to detail and commitment to quality.
  • Advanced proficiency with Microsoft Office and clinical trial management systems.
  • Ability to effectively collaborate across global teams and cultures.
  • Demonstrated commitment to customer service, operational excellence, and continuous improvement.


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.

About IQVIA

Innovex offers superior and creative advice to corporations. In addition, they raised venture capital for our own affiliate companies, in addition to having assisted clients in fund-raising efforts, new venture outreaches, and financing. Their engineers and technical staff offer varied backgrounds in manufacturing, high tech, product design, quality control, safety, biomechanics, and robotics.

IQVIA Careers

Join the vibrant team at IQVIA, a leading global provider of advanced analytics, technology solutions, and clinical research services to the healthcare industry. IQVIA is recognized for its commitment to innovation, leadership in healthcare, and a culture that celebrates diversity and inclusion.

Work You’ll Do

At IQVIA, we offer job opportunities that empower you to leverage your skills and drive healthcare forward. Become part of a team that thrives on innovation and the pursuit of operational excellence, helping to improve patient outcomes across the globe.

Transform Your Career

IQVIA is the place where you can transform the world of healthcare while advancing your career. With a variety of positions available, from research and development to business analytics, IQVIA is at the forefront of the industry. Our leadership is committed to fostering a culture of growth and professional development, making IQVIA a prime environment for both seasoned professionals and those seeking an internship to kickstart their career.

Innovative Work Environment

Join over 50,000 dedicated professionals in a dynamic environment where technology meets healthcare. At IQVIA, innovation isn’t just a buzzword; it's the backbone of how we solve complex challenges. With cutting-edge resources and a collaborative global team, your work at IQVIA directly contributes to advancements in life sciences.

Career Development and Benefits

IQVIA believes in nurturing its team members not just as employees but as individuals seeking to grow their careers. We support this with unmatched benefits, diversity training, and opportunities for leadership development. Our commitment to your career growth is matched by our dedication to providing a supportive and inclusive workplace.

Explore Job Opportunities

Whether you’re looking for a full-time position, part-time work, or a graduate internship, IQVIA offers a range of employment options to match your career ambitions. Our hiring process is designed to be transparent and engaging, helping you to understand where your skills can best be utilized within the company.

Networking and Professional Development

At IQVIA, networking and professional development are part of our DNA. Engage with industry leaders, participate in global conferences, and take advantage of our in-house training programs designed to enhance your skills and advance your career.

Stay Connected

Join Our Team Search open positions that match your skills and interests. We look for passionate, curious, creative, and solution-driven team players. Explore the diverse job opportunities at IQVIA and find where you can make an impact.

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Personalize your subscription to receive job alerts, latest news, and insider tips tailored to your preferences. Discover the exciting and rewarding career opportunities that await at IQVIA. Embark on a journey of growth, innovation, and leadership at IQVIA. Shape your future in an environment that values diversity and fosters professional development. Join IQVIA today and transform healthcare through the power of information and technology.
Learn more about IQVIA
Size
82,000 employees
Market Cap
$37.5 billion
Industry
Pharmaceuticals & Biotech
Net Income
$279 million
Founded
2016
5 Year Trend
+15.3%
Revenue
$11.3 billion
NASDAQ
IQV
* Ladders Estimates

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