Project Manager

Project Manager

Join Us at Centricity Research!

Centricity Research is one of the largest clinical research networks in North America. We are a fully centralized Integrated Research Organization (IRO) specializing in conducting Phase I-IV clinical trials in over 35 therapeutic areas: inpatient and outpatient; pharmaceutical, biotechnology, and medical device trials.

About the Role

As a Project Manager, you’ll be at the center of our clinical trial operations – making sure assigned studies launch on time, run smoothly, and meet enrollment goals. You’ll be the go-to connector between our research sites, internal teams, CROs, and sponsors, ensuring communication flows, challenges are tackled early, and every milestone is achieved. This is a fast-paced, problem-solving role where you’ll use your organizational skills and industry know-how to keep complex studies moving forward without missing a beat.

What You’ll Do

• Oversee assigned clinical trials from activation through close-out, keeping timelines, quality standards, and contractual deliverables on track.
• Act as the operational bridge between site teams, internal departments, and sponsors – making sure everyone stays aligned and informed.
• Spot and address potential risks before they impact study progress or quality.
• Monitor recruitment performance and implement targeted action plans to hit or exceed enrollment goals.
• Present concise, data-driven study updates to internal leadership and sponsor stakeholders.
• Represent the organization in sponsor meetings, advocating for resources, timeline adjustments, or protocol clarifications.
• Capture lessons learned and contribute to continuous process improvements across the network.
• Align all work with the organization’s mission, values, and OKR framework.

You Might Be a Great Fit If You:

• Bring at least 2–3 years of hands-on project management experience — this is essential for success in this role.
• Have experience in clinical research, preferably with exposure to site-level operations.
• Hold a bachelor’s degree in life sciences, healthcare, or a related field (or equivalent experience).
• Have a track record of meeting study start-up and enrollment targets.
• Know your way around GCP, ICH guidelines, and regulatory requirements.
• Communicate clearly and confidently — whether you’re presenting to leadership, negotiating with sponsors, or collaborating with site staff.
• Can juggle multiple priorities while keeping a calm, solutions-focused approach.
• Are comfortable using Microsoft Office and project management tools to keep everyone aligned.

Why Centricity Research?

Our Mission

We connect people to scientific advancements through groundbreaking research within a deeply human experience.

Our Core Values

• Quality : We aim for excellence and integrity in everything we do - because lives depend on it.
• Care : We show up for each other, our customers, and our mission - always going the extra mile.
• Be the Change You Seek : We're adaptable, forward-thinking, and constantly improving - for the betterment of all.
• One Team : We collaborate, support one another, and succeed together.
• Grow for Good : We grow with purpose - to expand access to research and improve global health.
• Own It : We take initiative, deliver results, and follow through - with passion and accountability.

Benefits

• Comprehensive health, dental, and vision insurance
• Enhanced EAP – mental health support
• Flexible PTO + paid holidays
• Continuing education reimbursement
• 401(k) / RRSP with company match and immediate vesting

The starting salary range for this position is $65,000 - $80,000 depending on experience.

EDUCATION/EXPERIENCE

• Minimum: o Education: Bachelors Degree
  • Experience: 1-2 Years of related Project Management experience (Analyst, Coordinator, Project Manager)
• Preferred: o Education: Masters Degree
  • Experience: 2-5 Years of direct Project Management experience o Licenses/Certifications from respected programs (ASQ, ACRP, PMI, etc.)

CORE COMPETENCIES/SKILLS

Prerequisite (Essential):

• Excellent communication skills (verbal and written)
• Excellent computer skills (MS Word, Excel and Outlook)
• Attention to detail
• Ability to manage time efficiently
• Self-directed
• Teamwork & Collaboration
• Proficient level of clinical, interpretive, and analytical skills with organizational skills for project planning Flexible & Adaptable
• Strong knowledge of ICH GCP, FDA & HC Division 5 guidelines Foundation:
• Conflict resolution
• Receptive to feedback
• Empowering & Developing others
• Empathy Skills
• Planning and organizing skills
• Excellent problem-solving skills
• Achievement oriented
• Analytical ability
• Initiative
• Decision making Leadership:
• Forward thinking
• Innovative
• Creative
• Strategic thinking
• Self confidence
• Strong interpersonal skills

PHYSICAL DEMANDS

• Physical demands include but not limited to prolonged sitting, light lifting, standing, reaching, walking, and bending.
• Frequently required to complete work on the computer in a seated position

May be required to lift light boxes (10 - 20lbs)

WORKING CONDITIONS

• Modern medical office environment or home office environment
• Required to follow OSHA and CCOHS guidelines, in addition to other local healthcare regulations
• Required to perform duties in relation to HIPAA, PIDEDA, and other local privacy regulations
• Some positions may require overnight/weekend hours

BENEFITS

• Opportunities to work with internationally renowned physicians
• Comprehensive health benefits, competitive salary
• RRSP or 401(k) contribution matching
• Continued opportunities for growth & development; yearly education allowance
• Paid holiday closures and employee appreciation days off