Logo for Clario

Assistant Clinical Project Manager

Role overview

Qualifications

  • Bachelor’s degree required
  • 1 plus years of experience in pharmaceutical drug development, clinical trials, and/or clinical research preferred
  • Healthcare, medical experience, and/or clinical research preferred
  • Proficiency in Microsoft Office tools

Responsibilities

  • Support Clinical Project Managers in drafting project documentation and reviewing presentations
  • Participate in project meetings, training sessions, and client calls
  • Read and interpret clinical protocol documents
  • Liaise with cross-functional teams to ensure timely delivery of study milestones

Key facts

Other skills

  • Microsoft Office
  • Communication
  • Mentorship
  • Detail Oriented
  • Organizational Skills
  • Teamwork
  • Problem Solving

About the company

Clario logo

Clario

Contract Research Organizations (CRO)

Clario is a leading healthcare research and technology company that generates high quality clinical evidence for our pharmaceutical, biotech, and medical device partners. We offer comprehensive evidence generation solutions that combine eCOA, cardiac safety, medical imaging, precision motion, and respiratory endpoints. Since our founding more than 50 years ago, Clario has delivered deep scientific expertise and broad endpoint technologies to help transform lives around the world. Our endpoint data solutions have supported clinical trials over 26,000 times in more than 100 countries. Our global team of science, technology, and operational experts have supported over 60% of all FDA drug approvals since 2019. For more information, visit Clario.com

Company details

Company typeXLarge
IndustryContract Research Organizations (CRO)
Company size1001 - 5000

Your match analysis

See how your profile stacks up against this role.

We compared the job requirements to your profile to show where you're strong and where you fall short.

Job description

Clario, part of Thermo Fisher Scientific, is seeking a detail‑oriented Assistant Clinical Project Manager to support the successful execution of global clinical studies. In this role, you will work closely with Clinical Project Managers and cross‑functional teams to ensure high‑quality, timely delivery of clinical projects in a regulated environment. This position offers an excellent opportunity to build hands‑on experience in clinical research while contributing to our mission of transforming lives through better evidence.


What We Offer

  • Competitive compensation

  • Private health insurance

  • Engaging employee programs

  • Flexible work schedules

  • Attractive PTO plan

  • Flex workspace

What You’ll Be Doing

  • Support Clinical Project Managers in drafting project documentation and reviewing presentations

  • Participate in project meetings, training sessions, and client calls

  • Read and interpret clinical protocol documents

  • Liaise with cross-functional teams to ensure timely delivery of study milestones

  • Monitor internal data flow and task completion within agreed timelines

  • Respond to inquiries professionally and promptly

  • Communicate project status updates to clients

  • Verify imaging protocol compliance and manage related queries

  • Act as Project Manager when assigned PM is unavailable

  • Mentor and support Operations team members; provide feedback to Operations Manager

  • Follow up on outstanding items such as missing data or incomplete documentation

  • Assist in resolving client issues and serve as an additional point of contact

  • Adhere to Standard Operating Procedures (SOPs) and regulatory guidelines (GCP, ICH, FDA)

  • Contribute to SOP and process document updates and operational improvements


What We Look For

Education:

  • Bachelor’s degree required

Experience:

  • 1 plus years of experience working in pharmaceutical drug development, clinical trials, and/or clinical research preferred

  • Healthcare, medical experience, and/or clinical research, preferred

  • Proficiency in Microsoft Office tools

  • Ability to work independently and collaboratively in a fast-paced environment

  • Strong attention to detail and organizational skills

  • Excellent verbal and written communication skills

  • Professional and positive attitude

  • Availability to work in a hybrid model from San Jose

  • Travel requirement: 0–5%

At Clario, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.

Clario is an equal opportunity employer. Clario evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

Apply once. Then go straight to the hiring manager.

After you apply, unlock the direct contact details of the people who actually make the call. A quick follow-up makes you 5x more likely to land an interview.

MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
Unlocked after you apply
·

Project Manager Related jobs

Other jobs at Clario

Premium

Reach out to the hiring manager directly.

Gain access to the contact details of the hiring managers who actually decide, and reach out to network with them directly. That, plus more when you upgrade:

  • Full match report with fit score and gaps
  • Career diagnostics on how recruiters read you
  • Curated company matches and warm intros
  • 48h early access to new roles

Cancel anytime.