Skip to content

Open nowFirst seen 3 days ago

Sr. Clinical Project Manager

Lifelancer3,724 open roles

Pay
$93,100 – $232,800 a year
Where
Remote
Work mode
Remote
Get the CV for this job

From $25 per CV, paid once. No subscription.

Your applicationOpen nowSr. Clinical Project ManagerLifelancer · Remote
  1. YouYes, apply to this one.

  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on Lifelancer's own form.

The reply lands in your private mailbox

3×more interviews than doing it yourself with ChatGPT.

The clock on this job

Early applications get read.

12.1% of postings close within 7 days. Measured by our own scanner across the market.

Share of postings closed within
  1. 2.1%1 day
  2. 4.5%3 days
  3. 12.1%7 days
  4. 19.1%14 days
  5. 35.6%30 days
  6. 52.7%60 days
This job: first seen 3 days ago

The posting

Job Title: Sr. Clinical Project Manager

Job Location: Washington, District Of Columbia, United States of America

Job Location Type: Remote

Job Contract Type: Full-time

Job Seniority Level:

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.

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.

This job is curated by Lifelancer.

Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains.

Please apply via Lifelancer platform to get connected to the application page and to find similar roles.

From $25, paid onceGet the CV for this job

What happens when you press

One press. We do the rest.

  1. A CV for this posting

    Written against Lifelancer's own wording, from every piece of relevant proof in your profile.

  2. 25 readers review it

    Recruiter, hiring manager, skeptic and more read every draft, round after round. You get the best round.

    The review screen in CV Rocket: how each CV was read, round by round.
  3. We apply on Lifelancer's form

    Our application engine gets through the hardest forms there are. Where a question needs you, AI suggests the best answer. Don't want us applying from our IP addresses? Use our Chrome extension: we apply straight from your own browser.

    An application in CV Rocket: every answer filled in on the employer's form.
  4. Every reply, sorted

    Lifelancer's answer lands in your private mailbox, and we classify it on arrival: interview, question, rejection.

    The CV Rocket inbox: each employer reply classified as an interview, an action or a rejection.
  5. Reply with AI

    AI helps you write the email, checks it and sends it. We show you whether the recruiter read it.

  6. The interview in your calendar

    Full integration with your calendar. The invitation goes straight in.

    An interview invitation in the CV Rocket inbox, added to the candidate's calendar.
Get the CV for this job

From $25 per CV, paid once. No subscription.

Why it works

3×

more interviews than doing it yourself with ChatGPT.

ChatGPT writes a CV and never learns what happened to it. We see every reply. For each CV we know:

  • How it was written, and how the review scored it
  • When we applied, and how long after the posting went up
  • Which posting, which company, which city
  • Who got the interview, and who heard nothing

That is how we know which CVs get called.

Get the CV for this job

From $25 per CV, paid once. No subscription.

The numbers game

More applications. More interviews.

Every application goes out with its own CV, written for that posting and paid once. Send enough of them and the law of large numbers finds you the job.

By hand5–10
With CV Rocket100
applications a day

Before you press

Straight answers

Get the CV for this job

From $25 per CV, paid once. No subscription.

What if my background isn't good enough?

We make the most of the background you have. The CV uses every piece of relevant proof your profile holds, and one of the 25 readers reads your whole profile and flags what the CV left out.

Do you really apply for me?

Yes, on the employer's own form, the hardest ones included. Where a question needs you, you answer it right there and AI suggests the best answer. Don't want us applying from our IP addresses? Use our Chrome extension: we apply straight from your own browser.

Is it a subscription?

No. You pay once per CV, from $25. Every application goes out with its own CV, written for that posting.

One job. One CV.
Paid once.

Pick the posting you want. We write for it, apply for you and catch the reply.

Get the CV for this job

From $25 per CV, paid once. No subscription.