Project Manager - Clinical

Alimentiv is a global CRO with a singular focus: advancing therapies for patients with gastrointestinal diseases. GI is our WHY and for more than 30 years that purpose has driven our scientific rigour, operational excellence, and deep therapeutic expertise, including supporting more than 70% of IBD compounds in development.
We operate as a private, profit-with-purpose company, channeling our commercial success back into scientific research, technology, and our people. With approximately 700 people across multiple countries and three service lines, we are growing deliberately, and the capability of our leaders and our organization is central to how we get there.

If you want to do meaningful work, build something real, and invest back in research that changes lives — we want to meet you!

What We Offer

In addition, as an Alimentiv Employee, you’re also eligible for the following programs:

• Education Reimbursement program for full-time employees
• Monthly Cell Phone and Remote Work Allowance (dependent on role eligibility)
• One time office setup allowance (can be used to purchase a scanner/printer, extra monitor, office furniture, etc.)
• Working while visiting program – up to 4 weeks per year!
• Flexible Summer Hours Program from May – September
• Employee referral incentive – we know great people know other great people, and we think that warrants recognition!
• Full-time employees also become beneficiaries of the Alimentiv Trust after one year of employment, and permanent members after 5 years of employment
• Optional formal mentorship program (Alimentorship); country/region annual social events in person; leadership development programs for people leaders in accordance with your seniority; social committee and several other optional initiatives designed to support you in feeling like part of the Alimentiv team!

Additional benefits may be available depending on the country of employment and are subject to local policies and eligibility.

Our Services

End-to-end GI clinical trial services, from protocol design through submission support
Central medical imaging management and endoscopic reading
Precision medicine and biomarker solutions
Real-world evidence and clinical consulting
Histopathology and lab services through AcelaBio

How to Apply

To apply for this position, please submit your resume through the Alimentiv Careers Portal or via LinkedIn’s Easy Apply. Resumes must be submitted in English.

Equal Opportunity and Accessibility

Alimentiv is committed to building a diverse, inclusive and respectful workplace. We are an equal opportunity employer and consider all qualified applicants for employment without regard to race, colour, ethnicity, national origin, religion or belief, sex, gender identity or expression, sexual orientation, age, marital or family status, disability, or any other characteristic protected by applicable law. 
 
Accommodations are available upon request for persons with disabilities throughout the recruitment and selection process. Requests can be directed to [email protected].

About the Role

Lead the planning, execution, monitoring, and successful completion of assigned clinical research projects, ensuring delivery against timelines, budgets, quality standards, and project objectives.

Lead and coordinate cross-functional project teams, ensuring clear accountability, effective collaboration, and timely completion of project deliverables.

Serve as the primary point of contact for sponsors and clients throughout the project lifecycle, managing expectations, providing regular updates, and proactively resolving issues.

Oversee project activities to ensure compliance with applicable regulatory requirements, clinical research guidelines, and corporate policies.

Manage project documentation, tools, and resources, ensuring appropriate development, maintenance, and delivery of essential study materials and records.

Monitor project performance, identifying risks, addressing operational challenges, and implementing solutions to maintain project quality and timelines.

Coordinate key project activities, including site monitoring, data management, patient safety, statistical analysis, and final reporting, in collaboration with functional experts.

Support project planning and execution through effective stakeholder communication, project meetings, training, and vendor coordination as required.

What we're looking for

• Education/Experience: Bachelor's degree in a relevant discipline with 1–3 years of related experience, or a college diploma/degree with 4–6 years of related experience.

Required Language Skills: English and Mandarin required. 
Highly Desirable: Medical Imaging exposure and expertise
 
Other:
Background in Health Sciences, Life Sciences, or Clinical Research is preferred (Equivalent combinations of education and relevant experience, supported by ongoing job-related training, will be considered)
Experience with project or financial resource management, including budget oversight and expenditure management.
Strong communication and interpersonal skills, with the ability to engage diverse internal and external stakeholders, navigate complex discussions, and appropriately escalate issues.
Demonstrated ability to work independently, exercise sound judgment, and prioritize competing responsibilities in a dynamic project environment.