Clinical Project Manager

Everest Clinical Research; Bridgewater (MA); Remote; USD 90,000 - 120,000; Full time

Job summary

Everest Clinical Research is seeking a Clinical Project Manager to oversee project delivery, ensuring compliance and quality. This role involves managing clinical operations, coordinating teams, and developing client relationships. The position can be remote within the USA or Canada.

Qualifications

• Minimum of 8 years of clinical research experience.
• Oncology experience preferred.

Responsibilities

• Managing projects across Everest service areas, ensuring milestones and deliverables are met.
• Facilitating project kick-offs, tracking progress, and managing budgets.
• Leading clinical trial phases in compliance with regulations.

Skills

Leadership

Communication

Problem-Solving

Fluency in Mandarin Chinese

Education

Bachelor’s or Master’s in life sciences

Job description

Join to apply for the Clinical Project Manager role at Everest Clinical Research.

Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of clinical research services to pharmaceutical, biotechnology, and medical device industries worldwide. Established in 2004 with headquarters in Markham, Ontario, Canada, and additional offices internationally, Everest is known for quality, customer service, and flexibility.

We are seeking a Project Manager for our Bridgewater, New Jersey, USA on-site location, or remotely from anywhere in the USA or Canada, to oversee project and portfolio delivery from start to finish, ensuring all aspects meet client and company expectations. Responsibilities include managing clinical operations, data management, statistics, medical writing, clinical trial technologies, and regulatory submissions, among others.

The role involves establishing project foundations, defining scope and budgets, planning and directing activities, managing resources, and reporting progress. The Project Manager will coordinate cross-functional teams, ensure compliance with regulatory standards, and maintain communication with sponsors and stakeholders.

Key responsibilities include:

1. Managing projects across Everest service areas, ensuring milestones and deliverables are met.
2. Facilitating project kick-offs, tracking progress, and managing budgets and resources.
3. Leading clinical trial phases in compliance with ICH, FDA, EMA, and other regulations.
4. Organizing meetings, communicating with teams and sponsors, and ensuring quality and timeliness of deliverables.
5. Managing project finances, tracking expenses, and reporting on performance.
6. Developing client relationships to foster repeat and new business opportunities.
7. Supporting operational and capability development activities, including SOPs, training, and technology tools.

Qualifications include a Bachelor’s or Master’s in life sciences or related field, a minimum of 8 years of clinical research experience, fluency in Mandarin Chinese, oncology experience preferred, and strong knowledge of regulatory guidelines. Leadership, communication, and problem-solving skills are essential.

For more information about Everest and other opportunities, visit our website. We are committed to diversity and providing accommodations for applicants with disabilities.