IQVIA

RWE Clinical Project Manager - Oncology (FSP)

IQVIA$93K — $232K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in life sciences or related field
  • 4-6 years of experience in project management or clinical operations
  • Demonstrated experience leading observational or real-world evidence studies
  • Strong understanding of RWE study designs and regulations
  • Experience with primary and secondary data study designs
  • Desired expertise in oncology therapeutic area

Responsibilities

  • Lead global observational study teams and ensure delivery of contracted scope and quality
  • Develop and maintain project management plans and study documentation
  • Ensure compliance with SOPs, policies, and effective study tools
  • Monitor study progress, including financial performance and forecasting
  • Manage vendor communications and related project activities
  • Anticipate and mitigate operational and quality risks
  • Generate project metrics and reports for senior management
  • Capture lessons learned for continuous improvement

Benefits

  • Health and welfare benefits
  • Potential incentive plans and bonuses
  • Opportunities for continuous professional development
  • Collaborative work environment with cross-functional teams
Full Job Description
Job Overview

In this role, the clinical project manager will be responsible for end-to-end project delivery of real-world observational studies within the oncology therapeutic area. It is important for this individual to have experience working in observational research across primary and secondary data collection study designs as well as leading clinical studies independently.

Who do you work with?
  • Epidemiologists, data science, and clinical leads to deliver project specific goals and timelines
  • Vendors to communicate status of deliverables and workflow
  • Program and business leads to manage full portfolio of projects


What are you great at?
  • Independently executing observational and real-world studies while balancing speed, quality, and cost
  • Leading cross-functional teams to achieve milestones and resolve study issues
  • Proactively identifying risks and implementing mitigation plans
  • Communicating clearly with stakeholders, including preparing and presenting project updates to leadership
  • Good understanding of project financials including experience managing, contractual obligations and implications
  • Driving operational excellence and strategic partnership with clients
  • Managing vendors effectively across different sourcing models (in-house, hybrid, outsourced)
  • Bringing clarity to complex or ambiguous situations and making informed decisions
  • Results-oriented approach to work towards delivery and output
  • Strong organizational, prioritization, and time management skills
  • Ability to operate effectively in a matrixed, fast-paced, and evolving environment


Your responsibilities may include:
  • Leading global, cross-functional observational study teams and owning delivery of contracted scope, timelines, and quality
  • Developing study documentation, including project management plans
  • Ensuring consistent use of study tools, training materials, and compliance with SOPs, policies, and procedures
  • Monitoring study progress and financial performance; supporting forecasting and change control as needed
  • Lead project vendor management related activities and communications per project requirements
  • Anticipating operational and quality risks, responding to issues raised by the project team and planning/implementing appropriate corrective or preventative actions
  • Generating project- or program-level metrics and reports for senior management
  • Capturing lessons learned and contributing to continuous improvement and best practices


Required knowledge, skills, and abilities
  • Bachelor's degree in life sciences or related field
  • Minimum 4-6 years of experience in project management and/or clinical operations within pharma, CRO, or RWE environment (or equivalent combination of education, training, and experience)
  • Demonstrated experience leading observational or real-world evidence studies
  • Strong understanding of RWE study designs and clinical research conduct and skill in applying applicable clinical research regulatory requirements
  • Experience with primary and secondary data study designs
  • Therapeutic area expertise desired (oncology)


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.

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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.

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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.

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Learn more about IQVIA
Size
82,000 employees
Market Cap
$37.5 billion
Industry
Net Income
$279 million
Founded
2016
5 Year Trend
+15.3%
Revenue
$11.3 billion
NASDAQ

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