Assistant Clinical Project Manager

Clario; Philippines; Hybrid; PHP 600,000 - 900,000; Full time

Benefits offered by this job

Private health insurance

Flexible work schedules

PTO plan

Flexible workspace

Competitive compensation

Engaging employee programs

Job summary

Clario is seeking an Assistant Clinical Project Manager to support global clinical studies within a regulated environment. You will work with Clinical Project Managers and cross‑functional teams to ensure high‑quality, timely delivery of study milestones, while expanding hands‑on experience in clinical research and maintaining SOP adherence.

The role emphasizes collaboration, data integrity, and effective communication with clients, with hybrid work options and a focus on regulatory compliance

Qualifications

• Bachelor’s degree required.
• 1+ 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.
• Availability to work in a hybrid model from San Jose.

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.
• 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.

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.

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.

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%

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.

Clario Privacy Policy

Clario is a leading provider of endpoint data solutions to the clinical trials industry, generating high-quality clinical evidence for life sciences companies. We offer comprehensive evidence generation solutions that combine medical imaging, eCOA, precision motion, cardiac solutions and respiratory endpoints. For more than 50 years, Clario has delivered deep scientific expertise and broad endpoint technologies to help transform lives around the world. Our endpoint data solutions have supported over 30,000 clinical trials in more than 100 countries. Our global team of science, technology, and operational experts have supported over 70% of all FDA drug approvals since 2015.