Sr. Clinical Research Associate

Allucent; Canada; Remote; CAD 80,000 - 110,000; Full time

Job summary

A leading company in the biopharmaceutical sector is seeking a Senior Clinical Research Associate based in Canada. This remote position involves monitoring clinical trials across various phases, ensuring compliance with regulations, and mentoring junior staff. Ideal candidates will have extensive experience in oncology or complex trials and be strong communicators who thrive in collaborative settings.

Benefits

Comprehensive benefits package

Competitive salaries

Flexible working hours

Leadership and mentoring opportunities

Professional development budget

Qualifications

• Minimum of 5 years’ experience in clinical research monitoring.
• Strong understanding of ICH-GCP and regulatory guidelines.
• Comfortable in an agile, collaborative environment.

Responsibilities

• Manage all aspects of monitoring for assigned clinical trials.
• Ensure compliance with protocols and regulatory requirements.
• Mentor and support junior CRAs in their professional growth.

Skills

Leadership

Clinical Monitoring

Communication

Education

Bachelor’s Degree in Life Sciences or related field

Job description

Bring your monitoring expertise to the forefront of innovation. We are looking for a Sr. Clinical Research Associate (Sr. CRA) to join our Canada-based A-team (remote; with travel). As a Sr. CRA at Allucent, you will independently control and monitor investigational sites, pro-actively detect issues, provide solutions to ensure clinical studies are performed according to the trial protocol and in compliance with SOPs, applicable regulations, and the principles of Good Clinical Practice.

At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. At Allucent we are big enough to deliver and small enough to care. We know all our colleagues by name and work together as a team to make everyone SHINE.

**This is a posting for multiple positions across Canada.**

The role

As a Sr. CRA, you will take the lead on monitoring activities, owning your sites and relationships with investigators. You’ll be the bridge between sponsor and site, ensuring trial integrity while being supported by a collaborative, experienced team. You will be a mentor for junior team members and contribute to grow our success. You will travel throughout the United States.

Main responsibilities:

• Independently manage all aspects of monitoring for assigned clinical trials across study phases, including site initiation, routine monitoring, and close-out visits.
• Ensure compliance with protocols, GCP, ICH, SOPs, and applicable regulatory requirements.
• Build strong site relationships, acting as a primary point of contact and ensuring high-quality data collection.
• Identify and resolve site issues, escalating as needed to maintain trial integrity and patient safety.
• Mentor and support junior CRAs, sharing knowledge and best practices.

Who are we looking for:

You’re an experienced CRA / monitor ready to take the next step with a company that truly values your expertise and independence. You thrive in an agile, collaborative environment and want to be part of a team making a real impact.

• Experience leading monitoring activities in complex trials in oncology, vaccines, and/or cell & gene therapy (CGT) and/or radiopharmaceuticals with a minimum of at least 5 years’ experience
• Strong understanding of ICH-GCP and regulatory guidelines.
• Clear and confident communicator in English.
• Comfortable working independently and managing priorities.
• Willingness to travel throughout the USA, as required.
• Effective clinical monitoring skills (all kind of visits mastered)

Benefits of working at Allucent include:

• Comprehensive benefits package per location
• Competitive salaries per location
• Departmental Study/Training Budget for furthering professional development
• Flexible Working hours (within reason)
• Opportunity for remote/hybrid* working depending on location
• Leadership and mentoring opportunities
• Participation in our enriching Buddy Program as a new or existing employee
• Internal growth opportunities and career progression
• Financially rewarding internal employee referral program
• Access to online soft-skills and technical training via internal platforms
• Eligibility for our Spot Bonus Award Program in recognition of going above and beyond on projects
• Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees

Apply now!

If you are interested in this role please apply through the button or for more information reach out to Tiffany Wasti at [e-mail]

Disclaimers:

*Our policy encourages a dynamic work environment, prescribing a minimum of 2 days in office per week for employees within reasonable distance from one of our global offices.

“The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively “Allucent”). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources.”

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