Research Coordinator Non-Licensed - Critical Care

Nova Scotia Health Authority; Halifax; On-site; CAD 60,000 - 80,000; Full time

Job summary

An established industry player in health services is seeking a Research Coordinator to lead and manage critical care research projects. This role involves coordinating clinical trials, overseeing participant recruitment, and ensuring compliance with research protocols. The ideal candidate will possess a strong background in health sciences, excellent analytical skills, and the ability to work collaboratively within a multidisciplinary team. Join a passionate and diverse team dedicated to improving health outcomes while enjoying a balanced lifestyle in the beautiful province of Nova Scotia.

Benefits

Health Insurance

Dental Insurance

Travel Insurance

Long-term Disability Insurance

Life Insurance

Defined Benefit Pension Plan

Qualifications

• Bachelor's degree in health sciences and significant research experience required.
• Master's degree preferred with GCP and TCPS-2 Certification.

Responsibilities

• Coordinate research projects and manage participant recruitment.
• Oversee daily operations of clinical research and maintain documentation.

Skills

Research Coordination

Analytical Thinking

Interpersonal Skills

Time Management

Communication Skills

Medical Terminology

Database Management

Education

Bachelor's Degree in Health Sciences

Master's Degree

Tools

MS Office

Email

Job description

Click here to apply as an internal applicant.

Req ID: 202286
Location: Central Zone,Halifax Infirmary Robie Street Entrance - QEII
Department: RSH Critical Care 891489
Type of Employment: Casual Hourly FT long-assignment (100% ) x 1
Management/Non Union P osition
Posting Closing Date: 19-May-25

Nova Scotia Health is the largest provider of health services in Nova Scotia, with some specialized services also offered to clients throughout Atlantic Canada. We’re on a mission to achieve excellence in health, healing, and learning through working together, which is reflected in the hospitals, health centres, and community-based programs we operate across the province. Our passionate team of professionals provides a variety of high-quality inpatient and outpatient services including academic, tertiary, and quaternary care, as well as continuing care, primary health care, public health, and mental health and addictions. Join a diverse team of innovators, collaborators, and creative thinkers today.

Nova Scotia Health employs professionals in all corners of our beautiful province. We believe there's a place here for everyone to call home, from vibrant cities with exuberant nightlife to quaint towns with picturesque trails. The work-life balance that comes with a Nova Scotia Health role means you'll have the time to explore, discover, and participate in that coveted Atlantic lifestyle. Visit us today and check out www.novascotia.com to see why more people from across the globe are moving here.

About the Opportunity

Reporting to the Critical Care Research Director and Manager of the Dalhousie Critical Care Department, the Research Coordinator is responsible for the coordination of research projects conducted within the Department of Critical Care. This coordination includes the administration of the study/clinical trials,document management, participant recruitment, data collection, chart reviews, laboratory testing, and follow up visits. They oversee the daily operation of clinical or non-clinical research within the Department of Critical Care. This includes acting as a resource and support for staff and learners (i.e., medical students, residents, and fellows) involved in research, in order to facilitate consistency within the research program.The Research Coordinator is responsible to provide clinical leadership, guidance, and support to determine the overall direction of research study activities and participant involvement in respect to the study under the direction of the Primary Investigator (PI).

SPECIFIC ACCOUNTABILITIES

(Incumbent may perform any combination of the following duties).

• Orient and supervise research nurses and research assistants in the conduct of the study protocol
• Coordinate and perform study screening, recruitment, bookings, enrollments, and follow-up
• Ensure study documentation and study files are appropriately maintained
• Educates and updates hospital staff on study protocols
• Obtains informed consent
• Acts as the initial point of contact for study subjects to answer questions or address problems and follows up as appropriate
• Participates in various hospital rounds and meetings with either the PI or the division/department
• Obtains medical and family history as it relates to the study
• Administers questionnaires as per the protocol
• Responds to study subject inquiries by phone and in person
• Manages database forms/questionnaires and ensures their accuracy and completion
• Creates source documents
• Reviews health records
• Maintains documentation related to research ethics approval and monitoring
• Monitors budgets and provides reports as required
• Facilitates the collection of payments from the sponsor
• Monitors study timelines
• Confers with the PI and sponsor representatives on study progress, compliance and interpretation
• Performs literature reviews
• Writes reports as needed

About You

We would love to hear from you if you have the following:

• Completion of a Bachelor’s degree in health sciences with significant research work experience required
• Master’s degree preferred
• GCP and TCPS-2 Certification
• Familiarity with patient screening and informed consent required
• Familiarity with reading and interpreting health records an asset
• Effective research and analytical thinking skills
• Experience with trials, chart reviews/literature reviews an asset
• Medical Terminology course preferred
• Relevant clinical experience considered an asset
• Proficiency in MS Office (Word. Access, Excel, PowerPoint), email and internet
• Effective interpersonal and communication skills
• Demonstrated time management and organizational skills
• Ability to work well independently as well as within a multidisciplinary team environment
• Demonstrated research and analytical thinking skills
• Strong negotiation, conflict resolution and rapport-building skills
• Competencies in other languages an asset, French preferred

Please ensure your resume and cover letter is up to date and includes all relevant education, experience, training, and certifications.

Hours

• Long Assignment, Full-Time / 75Hours Bi-weekly
• June 2025 to June 2026, 12 months

Compensation and Benefits

$27.45 - $34.32 Hourly

Successful candidates may be eligible for our benefits package which includes health, dental, travel, long-term disability, and life insurance coverage as well as a defined benefit pension plan.

Once You've Applied

Thank you for your interest in this position. Only those applicants selected for an interview will be contacted.

Nova Scotia Health is committed to being a workforce that is free of discrimination, values diversity, and is representative, at all job levels, of the people we serve. We encourage all qualified applicants who self-identify as Indigenous, Black/African Nova Scotian, Persons of Colour, Foreign Nationals/Newcomers, Persons with Disabilities, 2SLGBTQIA+ to apply and self-identify.