Current jobs related to Clinical Research Coordinator Ii - Toronto - Centricity Research

  • Clinical Research Coordinator

    1 week ago

    Toronto, Canada Clinical Research Full time

    Responsibilities: - Coordinate and oversee clinical research studies from start to finish - Collect and record data accurately and efficiently - Analyze research data and prepare reports for review - Ensure compliance with study protocols, regulations, and ethical guidelines - Collaborate with healthcare professionals, researchers, and study participants -...

  • Clinical Research Coordinator Ii

    1 week ago

    Toronto, Canada Syneos - Clinical and Corporate - Prod Full time

    **Description** Clinical Research Coordinator II Illingworth Research Group provides a range of patient focused clinical services to the pharmaceutical, healthcare, biotechnology and medical device industries. These include mobile research nursing, patient concierge, medical photography and clinical research services. Illingworth are experts with...

  • Senior Clinical Research Associate

    2 weeks ago

    Toronto, Canada Everest Clinical Research Services Inc Full time

    Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical...

  • Clinical Research Coordinator

    1 week ago

    Toronto, Canada Psychedelic Research Consultants Inc. Full time

    Clinical Research Coordinator Psychedelic Research Consultants is a Canadian based consulting firm dedicated to the advancement of psychedelic science and therapeutics. We are looking for an experienced full-time Toronto based Clinical Research Coordinator (CRC) to work directly with the Principle Investigator (PI) and Research Director on assigned...

  • Clinical Research Coordinator

    1 week ago

    Toronto, Canada Headlands Research Full time

    **Overview**: **The Role** Toronto Memory Program is looking for a Clinical Research Coordinator to manage clinical research protocols. This individual will work directly with the investigators, and other research staff to ensure protocol visits are being conducted according to ICH GCP guidelines. **This Clinical Research Coordinator role will be based in...

  • Clinical Research Coordinator

    1 week ago

    Toronto, Canada Headlands Research Full time

    Overview: **The Role** Toronto Memory Program is looking for a Clinical Research Coordinator to manage clinical research protocols. This individual will work directly with the investigators, and other research staff to ensure protocol visits are being conducted according to ICH GCP guidelines. **This Clinical Research Coordinator role will be based in...

  • Clinical Research Coordinator

    5 days ago

    Toronto, Canada Centricity Research Full time

    Position Title: Clinical Research Coordinator I (CRCI) Department: Clinical Operations Reports To: Operations Manager, Assistant Operations Manager Direct Reports: N/A POSITION FUNCTION The Clinical Research Coordinator I (CRC I) perform a variety of administrative and clinical activities to assist the Investigators in conducting clinical studies. The...

  • Clinical Research Coordinator

    3 days ago

    Toronto, Canada Centricity Research Full time

    LMC Manna Research, IACT Health, and True North Clinical Research have united to become the largest network of fully-owned and integrated clinical research sites in North America, Centricity Research. The sites that were formerly known as LMC Manna bring phase I-IV clinical trial services with specialized focuses on endocrine disorders, real world evidence...

  • Clinical Research Safety Associate

    2 weeks ago

    Toronto, Canada Everest Clinical Research Services Inc Full time

    Everest Clinical Research ("Everest") is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in...

  • Clinical Research Safety Associate

    2 weeks ago

    Toronto, Canada Everest Clinical Research Services Inc Full time

    Everest Clinical Research ("Everest") is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in...

Clinical Research Coordinator Ii

2 weeks ago

Toronto, Canada Centricity Research Full time

**Clinical Research Coordinator II (CRC II)**

**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**

We’re looking for a Clinical Research Coordinator II (CRC II) to support the successful execution of clinical studies through advanced administrative and clinical responsibilities. Building on at least two years of experience as a Clinical Research Coordinator, you’ll play a key role in ensuring study activities are carried out accurately, efficiently, and in full compliance with protocol and regulatory standards. In addition to managing your own workload, you may assist with training and mentoring Research Assistants (RAs) and CRC Is.

**What You’ll Do**

**Study Coordination & Participant Safety**
- Conduct study visits in accordance with protocol, GCP, SOPs, and regulatory requirements
- Ensure the safety and well-being of all study participants, reporting and documenting adverse events appropriately
- Perform clinical tasks such as phlebotomy, ECGs, vitals, sample collection, and investigational product handling
- Maintain accurate source documentation, CRFs, CTMS entries, and query resolution

**Recruitment, Screening & Enrollment**
- Support recruitment initiatives to identify and enroll eligible study participants
- Screen participants against inclusion/exclusion criteria
- Guide participants through the informed consent process and ensure documentation accuracy
- Coordinate study visits across the full participant lifecycle

**Study Execution & Data Integrity**
- Accurately complete study documentation, reports, and regulatory files
- Assist with preparation for monitoring visits, audits, and inspections
- Perform regular quality control checks on study data and records
- Collaborate with investigators, management, and sponsors to ensure smooth study conduct
- Participate in site feasibility questionnaires (FQs) and pre-study visits (PSVs) to support site readiness and study start-up activities

**Team Support & Mentorship**
- Share knowledge and assist with training Research Assistants (RAs) and CRC Is
- Provide day-to-day guidance to junior team members on protocol compliance and study procedures
- Support site operations by helping maintain lab supplies, equipment, and administrative needs
- Participate in site meetings, sponsor trainings, and community engagement events as needed

**You Might Be a Great Fit If You**:

- Have a bachelor’s degree in a health, science, or research-related field (or equivalent combination of education and experience)
- Have 2+ years of experience as a Clinical Research Coordinator (CRC)
- Are confident performing standard clinical research procedures (phlebotomy, vitals, ECGs, sample processing, investigational product handling)
- Enjoy collaborating with investigators, participants, and colleagues in a team-driven environment
- Are detail-oriented, organized, and proactive in balancing multiple studies
- Take pride in supporting and mentoring junior team members

**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

**Ready to Apply?**

We’re an equal opportunity employer committed to building a diverse and inclusive workplace. We welcome applicants from all backgrounds and will provide accommodations during the hiring process upon request.

EDUCATION/EXPERIENCE

**Minimum**:

- CAN: College/University degree in a relevant field of science
- US: HS/GED
- CAN/US: Depending on role requirements, specific degree and licensure from designated provincial/state body the location of the clinical site (ex. RN, MLT, etc.)
- Active BLS certification (for CPU setting)
- Proficient IV and phlebotomy skills (as applicable to the site requirements)
- CAN/US: ACRP Clinical Research Certification with at least 18 mont