Clinical Project Manager

Alimentiv; Rowley; Remote; GBP 72,000 - 119,000; Full time

Benefits offered by this job

Education reimbursement

Remote work allowance

Office setup allowance

4 weeks visiting program

Flexible Summer Hours

Referral incentive

Alimentiv Trust after 1 year

Mentorship program

Job summary

Alimentiv is seeking a motivated Clinical Project Manager to oversee planning, delivery, and regulatory compliance of clinical research projects. This home-based role involves coordinating cross-functional teams, managing timelines and budgets, and maintaining sponsor relationships.

Travel is occasional, and strong communication and organizational skills are essential. The ideal candidate has 1–3 years in clinical study management, a solid understanding of study documentation, and fluency in

Qualifications

• Bachelor's degree in Health Sciences, Clinical Research, or related field.
• 1–3 years of clinical study management experience.
• Strong knowledge of clinical research processes and regulatory requirements.
• Excellent project management and organizational skills.
• Effective written and verbal communication with sponsors and teams.
• Ability to collaborate across cross-functional teams.
• Detail-oriented with commitment to compliance and quality.
• Fluent English and ability to work remotely with travel.

Responsibilities

• Lead planning, execution, monitoring, and completion of assigned clinical research projects.
• Coordinate cross-functional project teams to ensure compliance with regulations, guidelines, policies, and quality standards.
• Oversee project operations, budgets, regulatory requirements, and patient safety.
• Manage development, maintenance, and disposal of essential clinical study documents and data.
• Assign, track, and oversee site monitoring, data collection, adverse event management, statistics, and reporting.
• Serve as primary contact for sponsors and clients, proactively managing expectations and issues.
• Organize and facilitate project meetings, provide investigator updates, and progress reports.
• Support site and patient recruitment strategies and training initiatives.
• Participate in regulatory submissions, audits, vendor selection, and related activities.

Skills

Clinical project management

Regulatory compliance

Budgeting

Communication

Cross-functional coordination

Attention to detail

Remote work

Education

Bachelor's degree in Health Sciences/Clinical Research

Job description

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!

Job Overview

We are seeking a motivated and detail-oriented Clinical Project Manager to oversee the planning, execution, and successful delivery of clinical research projects. In this role, you will coordinate cross-functional teams, manage project timelines and deliverables, ensure regulatory compliance, and maintain strong relationships with sponsors and clients.

The ideal candidate will possess excellent communication, organizational, and problem-solving skills, with a collaborative approach to achieving project objectives. This is a home-based opportunity with occasional travel.

Key Responsibilities

• Lead the planning, execution, monitoring, and completion of assigned clinical research projects, ensuring project objectives and deliverables are achieved.

• Coordinate cross-functional project teams to ensure activities comply with applicable regulations, industry guidelines, corporate policies, and quality standards.

• Oversee project operations, budgets, regulatory requirements, and patient safety to maintain operational and financial integrity throughout the project life cycle.

• Manage the development, maintenance, and appropriate disposal of essential clinical study documents, data, equipment, and tools, including protocols, SOPs, informed consent forms, and case report forms (CRFs).

• Assign, track, and oversee interdisciplinary activities, including site monitoring, database development, data collection, adverse event management, statistical analysis, and clinical study reporting.

• Serve as the primary point of contact for sponsors and clients, proactively managing expectations, resolving project-related issues, and maintaining effective communication.

• Organize and facilitate project meetings, prepare investigator updates, and provide regular project progress and status reports to relevant stakeholders.

• Support site and patient recruitment strategies, stakeholder training initiatives, and the development of study-related communication materials.

• Participate in regulatory submissions, audits, third-party vendor selection, and other activities required to support successful project delivery.

• Monitor team performance, project milestones, and deliverable quality to ensure alignment with sponsor expectations, project requirements, and regulatory standards.

Skills & Qualifications

• Bachelor's degree in a relevant field, preferably Health Sciences, Clinical Research, or a related discipline.

• 1–3 years of experience in clinical study management, with exposure to clinical research project coordination and execution.

• Strong understanding of clinical research processes, regulatory requirements, quality standards, and study documentation practices.

• Excellent project management and organizational skills, with the ability to coordinate multiple tasks, track deliverables, and meet project deadlines.

• Strong written and verbal communication skills, with the ability to interact effectively with sponsors, clients, investigators, and cross-functional teams.

• Demonstrated ability to build collaborative working relationships, encourage teamwork, and coordinate interdisciplinary project activities.

• Exceptional attention to detail, with a commitment to maintaining accuracy, compliance, and high-quality project outcomes.

• Self-motivated and results-oriented, with strong problem-solving skills and the ability to proactively identify and address project challenges.

• Commitment to continuous learning, professional development, and adapting to evolving project and organizational requirements.

• Fluency in English, including reading, writing, and speaking, with the ability to work effectively in a home-based environment and travel occasionally as required.

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

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 [e-mail].

$95,500 - $159,000 a year

Please note that the salary range may vary depending on the country in which the position is based.

Performance-Based Incentive Program

At Alimentiv, we recognize and reward great performance. In addition to a competitive salary, eligible employees can participate in our Short-Term Incentive Plan (STIP), which offers the opportunity to earn additional compensation based on individual contributions, team achievements, and company performance.