IQVIA

Associate Clinical Project Management Director, Cross TA

IQVIA • $93K — $285K *
Durham, NC 27713In-Person
Pharmaceuticals & Biotech
8 - 10 years of experience
Reposted Today
Be an Early Applicant
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Life Sciences or equivalent.
  • Minimum 8 years of experience in clinical trial management at a large pharmaceutical company.
  • Strong knowledge of ICH-GCP and local regulatory compliance.
  • Proven ability to lead cross-functional teams in global settings.
  • Excellent communication, decision-making, and analytical skills.
  • Experience with clinical systems like CTMS and TMF.
  • Ability to manage ambiguity and proactively find solutions.

Responsibilities

  • Lead the Study Management Team and track trial deliverables.
  • Ensure real-time progress documentation throughout the trial.
  • Maintain inspection readiness across all trial phases.
  • Serve as the primary contact for country and regional staff.
  • Collaborate with Global Trial Leads on central activities from start-up to close-out.
  • Address and resolve trial issues, contributing to corrective action plans.
  • Support site selection and feasibility assessments.

Benefits

  • Remote work opportunity with some travel required.
  • Supports career growth with opportunities for mentorship.
  • Offers a chance to work on complex, impactful clinical trials.
  • Access to a leading global company's resources and expertise.
Full Job Description
Position Overview:

IQVIA is seeking an experienced Associate Clinical Project Management Director/Trial Delivery Manager (TDM) to lead and coordinate global and regional clinical trial management activities. This role ensures the successful planning, execution, and closure of clinical trials, whether internally managed or outsourced. The TDM will serve as a key member of the Study Management Team (SMT), supporting trial leaders and interfacing with internal and external stakeholders to ensure compliance, quality, and timely delivery of trial milestones.

Key Responsibilities:

Trial Oversight & Management
  • Lead the Study Management Team and provide regular updates on trial deliverables.
  • Ensure real-time tracking and documentation of trial progress.
  • Maintain inspection-readiness throughout the trial lifecycle.
  • Act as the primary contact for country and regional staff and internal teams.
  • Partner with Global Trial Leads to oversee central trial activities from start-up to close-out.
  • Escalate and resolve trial issues and contribute to CAPA processes.

Site & Vendor Coordination
  • Support site selection and feasibility assessments.
  • Monitor enrollment commitments and ensure recruitment plans are in place.
  • Oversee selected vendors and review related deliverables and invoices.
  • Coordinate with vendors such as IVRS, Central Labs, ePRO, Imaging, Translation, and Ancillary Supplies.

Documentation & Compliance
  • Create and maintain trial-specific documents (e.g., Monitoring Guidelines, ICFs, Blinding Plans).
  • Ensure timely filing, archiving, and retention of trial documents.
  • Provide central documents for regulatory submissions.
  • Support Health Authority inspections and internal audits.

Training & Meetings
  • Develop and deliver trial-specific training materials.
  • Coordinate and participate in Investigator Meetings.

Budget & Financial Oversight
  • Establish country budgets and monitor actuals vs. forecast.
  • Understand Out-of-Pocket (OOP) and FTE cost drivers.


Qualifications:

Education:
  • Bachelor's degree in Life Sciences (Biology, Chemistry, Biochemistry, Nursing, Pharmacy) or equivalent.

Experience:
  • Level 2 (Advanced): Minimum 8 years of experience, with proven leadership in complex trials at a large pharmaceutical company.

Skills & Competencies:
  • Strong knowledge of ICH-GCP and local regulatory requirements.
  • Proven ability to lead cross-functional teams and manage global trials.
  • Excellent communication, decision-making, and analytical skills.
  • Proficiency in Microsoft Office, CTMS, TMF, and other clinical systems.
  • Experience in virtual team coordination and stakeholder engagement.
  • Ability to manage ambiguity and drive solutions proactively.


Preferred Attributes:
  • Monitoring or data management experience.
  • Experience in budget planning and financial oversight.
  • Ability to mentor junior CTMs and lead special initiatives or task forces.
  • Therapeutic area expertise and ability to act as protocol expert.


Metrics & KPIs:

Performance will be measured according to the Quality Oversight Plan (QOP) and trial-specific deliverables.

*This is a remote home-based role that may require some travel

The potential base pay range for this role, when annualized, is $93,100.00 - $285,500.00. 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.

Keep Up to Date

Stay ahead with career tips, insider perspectives, and industry-leading insights you can put to use today—all from the people who work here.

Job Alert Emails

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

Similar Jobs

Ad banner background

Get Ready For Your
Next Interview

More Jobs at IQVIA

More Pharmaceuticals & Biotech Jobs

Find similar Associate Clinical Project Management Director, Cross TA jobs:

NationwideDurham, NC