Clinical data coordinator Jobs

Clinical Research Coordinator
Dermatology Research Institute —Calgary, AB
- $28–$30 an hour
- Weekends as needed
- CPR Certification
- BLS Certification
- Master's degree
- Dental care
17h
Clinical Research Coordinator – Nurse - CIM - Oncology
Centre universitaire de santé McGill - Institut de Recherche —Montréal, QC
- $45,518.20–$105,996.80 a year
- 8 hour shift
- Nursing
- English
- Bachelor's
- Designated paid holidays
- Employee assistance program
Quick apply
Strategic Project Lead, Sciences – Toronto
Mecka —Markham, ON
- $150,000–$200,000 a year
- Full-time
- Hybrid work
- Laboratory experience
- Computer networking
Quick apply
Clinical Research Coordinator (Nurse)
Centre universitaire de santé McGill - Institut de Recherche —Montréal, QC
- Temporary
- Bilingual
- Nursing
- English
- Designated paid holidays
- Employee assistance program
Quick apply
Coordinator, Milk/Formula Handling Room - Royal Columbian Hospital
Fraser Health —New Westminster, BC
- $46.52–$58.07 an hour
- Word processing
- Supervising experience
- Bachelor's
Learning Communities and Evaluation Coordinator
ACCESS Open Minds Indigenous Youth Mental Health and Wellness Network —Verdun, QC
- $30–$48 an hour
- Full-time
- Hybrid work
- Doctoral degree
- Research
- Master's degree
Quick apply
5d
Research Technician
McGill University —Montréal, QC
- $33.05–$40.97 an hour
- Part-time
- Hybrid work
- English
- Bachelor's
- Dental care
- Paid time off
1d
Project Lead
McGill University —Montréal, QC
- $73,470–$110,210 a year
- Full-time
- Hybrid work
- Doctoral degree
- English
- Project management
- Dental care
- Paid time off
11h
Laboratory Coordinator
University of Alberta —Edmonton, AB
- Full-time
- Doctoral degree
- Laboratory experience
- Master's degree
- Dental care
Quick apply
10h
Research Assistant / Assistant(e) de Recherche
Lady Davis Institute - Jewish General Hospital —Montréal, QC
- $24.99–$32.61 an hour
- 8 hour shift
- Microsoft Powerpoint
- Bilingual
- Writing skills
- Disability insurance
- Dental care
Quick apply
Research Assistant
Centricity Research —Toronto, ON
- $45,000–$50,000 a year
- Full-time
- Medicine
Quick apply
1d
Caseworker – Nursing & Clinics - Bilingual - French
Cencora —Quebec City, QC
- Full-time
- Microsoft Powerpoint
- Bilingual
- Microsoft Word
- Dental care
- Paid time off
Licensed Practical Nurse
Alberta Health Services —Edmonton, AB
- $33.16–$43.42 an hour
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
21h

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Strategic Project Lead, Sciences – Toronto
Mecka —Markham, ON
Field experience leading or working with scientific teams: 2+ years running or supporting labs, field studies, or research operations — leading or working…
$150,000–$200,000 a year
Quick apply
Research Assistant
Centricity Research —Toronto, ON
Have a degree or diploma in biological sciences, medicine, healthcare, clinical research, or a related field, or an equivalent combination of relevant education…
$45,000–$50,000 a year
Quick apply
1d

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Clinical Research Coordinator

Dermatology Research Institute -
Calgary, AB

Apply Now

Job details

Permanent | Full-time
$28–$30 an hour
17 hours ago

Qualifications

CPR Certification
Phlebotomy
BLS Certification
Master's degree
Presentation skills
Organizational skills
Communication skills

Full job description

About Us:

Dermatology Research Institute specializes in clinical and epidemiological trials that focus on improving skin health. Founded by dermatologists, our team of accomplished physicians, trusted coordinators, and compassionate nurses are at the forefront of discovering new diagnostics and therapeutics. With a combined 11 years of experience, including over 100 unique studies for over 25 pharmaceutical companies, pediatric and adult patients can be certain they are receiving personalized solutions when it matters the most.

Mission Statement:

Dermatology Research Institutes takes great pride conducting industry-sponsored and investigator-initiated phase II, III, and IV studies for a broad spectrum of skin diseases and treatments in a fully equipped, state-of-the art facility with modern design, cutting-edge technology, efficient flow, and secure storage. We adhere to the most rigorous professional and ethical standards. Our highly-qualified staff pay meticulous attention to detail in terms of protocol compliance and data management, but also recognize the importance of creating a positive, safe, and comfortable environment for patients.

Vision:

Through consistency in meeting and/or exceeding enrolment targets as well as proficiency in presentation and publication of results, Dermatology Research Institute strives to become a respected leader for advancing medical knowledge. Contributing to scientific breakthroughs that will enhance the care of patients suffering from dermatologic conditions is what drives us.

Core Values:

Investigate
Interpret
Inform

The Role

Description:

The Clinical Research Coordinator (CRC) serves as the lead coordinator on multiple concurrent clinical trials (up to 10 studies) and is responsible for the execution of study protocols and the delivery of high-quality clinical research data, while ensuring optimal patient care in accordance with Health Canada and ICH-GCP standards.

This role is highly patient-facing and involves daily coordination of in-clinic patient visits, including screening, enrollment, and follow-up assessments.

The CRC provides comprehensive oversight and coordination of clinical trials conducted at the Dermatology Research Institute, including:

Acting as the primary point of responsibility for assigned studies, ensuring protocol adherence, regulatory compliance, and timely study execution
Coordinating patient recruitment, screening, and enrollment, including conducting detailed eligibility assessments
Leading daily patient visits, including study procedures, education, and ongoing participant support
Obtaining and reviewing informed consent, ensuring patients receive and understand all study-related information
Collecting, documenting, and managing clinical trial data with a high degree of accuracy and integrity
Maintaining study documentation, source records, case report forms, and electronic databases
Managing study timelines, resources, and competing priorities across multiple active trials
Liaising with patients, investigators, nurses, administrative staff, and pharmaceutical sponsors to ensure seamless study conduct

Job Type:

This is a full-time position. Availability on evenings and weekends may be required.

Incentives and Perks:

Consistent work hours and a commitment to work/life balance
Opportunity to work alongside a team of highly-skilled professionals
Extremely competitive wages
Health and dental benefits available
Ongoing paid training and professional development opportunities
Supportive team dynamics
Excellent mentorship and leadership
Safe, supportive and tolerant workplace

Qualifications

Required Education:

Degree in a relevant health-related field with subsequent experience or Master’s degree in health-related field
Equivalent combination of relevant experience and/or education/training

Required Certification:

Cardiopulmonary Resuscitation (CPR) / Basic Cardiac Life Support (BCLS) (preferred)
Phlebotomy/Venipuncture Certificate (preferred)
Society of Clinical Research Associates (SOCRA) Certification (preferred)

Required Experience, Knowledge & Skills:

Minimum 1 year prior experience as CRC leading clinical trials
Experience using clinical trial electronic case report form (eCRF) software (preferred)
Demonstrated clinical research experience and an ability to adhere strictly to research protocols and guidelines whilst remaining up-to-date with clinical trial trends and developments
Ability to perform phlebotomy/venipuncture (preferred)
Highly-developed planning and organizational skills with experience establishing priorities, implementing improvements and meeting deadlines while working effectively under pressure
Thorough understanding of human research ethics principles and familiarity with institutional ethics committee guidelines and Good Clinical Research Practice
Demonstrated ability to work as an effective member of a team, as well as, the ability to exercise high levels of independence, judgement and initiative
Demonstrated understanding of confidentiality, privacy and information handling principles coupled with the ability to work with sensitive information and maintaining discretion at all times
Highly-developed interpersonal and communication skills with the ability to prepare professional documentation for various audiences and provide expert advice in areas of clinical or research knowledge
Demonstrated relationship management skills, including the ability to interact with, negotiate and gain cooperation from internal and external stakeholders

Background Check:

A clear Criminal Background check, inclusive of a vulnerable sector search, is required to start. If you have resided outside of the city of Calgary in the past 12 months, you will need to contact the local police or RCMP detachment in your previous residential municipality to be able to obtain a full report.

Job Types: Full-time, Permanent

Pay: $28.00-$30.00 per hour

Education:

Master's Degree (required)

Experience:

Phlebotomy: 1 year (required)
medical writing: 1 year (required)

Location:

Calgary, AB T2H 1M5 (required)

Work Location: In person

Apply Now

Refine Your Search

Clinical Research Coordinator

Clinical Research Coordinator – Nurse - CIM - Oncology

Strategic Project Lead, Sciences – Toronto

Clinical Research Coordinator (Nurse)

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Research Technician

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Laboratory Coordinator

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Research Assistant

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Licensed Practical Nurse

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