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2400003805 - Clinical Research Coordinator I

  • Job
    Full-time
    Junior Level
  • Research & Development
    Healthcare
  • Ajax

AI generated summary

  • You need 2 years of clinical trial coordinator experience, GCP certification, knowledge of ethics, medical terminology, and strong organizational and communication skills.
  • You will support research operations, consent participants, manage documentation, ensure compliance, abstract data, communicate with stakeholders, assist ethics applications, and attend project meetings.

Requirements

  • 2 years experience working as a research coordinator in clinical trials
  • Current Good Clinical Practice (GCP), Division 5 and Tri-Council Policy Statement: Ethical Conduct for Research Involving Humans
  • Completion of a recognized clinical trials/research education program and/or recent related experience
  • Knowledge of medical terminology, anatomy, and physiology
  • Demonstrated knowledge of Research Ethics Board requirement for research
  • Demonstrated ability to organize and prioritize workload and function independent with minimum supervision
  • Proven ability to exercises skill and discretion when approached with issues of a sensitive nature
  • Proven excellent interpersonal and communication skills both written and verbal
  • Demonstrated understanding of and commitment to Lakeridge Health's comprehensive safety programs and practices including staff, patient and environmental safety and participation in regular in-service Education in this area

Responsibilities

  • Under nominal supervision, the Research Coordinator I performs a variety of research and clerical tasks and supports the clinical research team in the operations and conduct of clinical research according to defined practices and regulations. These duties include:
  • Participating in the execution and evaluation of multiple research projects;
  • Consenting participants according to protocol, guidelines, SOPs and regulatory requirements;
  • Preparing, handling, distributing, filing and archiving clinical research documentation according to protocol, standard operating procedures and regulatory requirements;
  • Acting as a key communicator between study personnel and sponsors, and liaise with investigators and study staff to ensure the consistency and quality of study procedures;
  • Screening for and identifying eligible study participants;
  • Abstracting data from source documents, performing data entry into electronic case report forms (eCRFs) in an accurate and timely fashion, and ensuring query resolution;
  • Interpretation of applicable regulations to ensure compliance;
  • Preparing research ethics board applications and assisting with maintaining study compliance on all terms;
  • Attending and participating in project-related meetings;
  • Producing written, tabular and visual materials for research reports and presentations;
  • Acting as a contact for the clinical research team for designated project communications, correspondence and associated documentation;
  • Completing additional tasks as needed to support the departmental needs;
  • The candidate will also be responsible for supporting the organization and co-ordination of all functions of the research projects, and other duties as assigned;
  • Travel to regional sites may be required;

FAQs

What is the job title for this position?

The job title is Clinical Research Coordinator I.

What is the duration of this position?

This position is temporary full-time for approximately 22 months.

What are the working hours for this role?

The working hours are 8-hour shifts during the day, although this is subject to change.

Where is the job located?

The job is located at Lakeridge Health Ajax-Pickering.

What is the wage schedule for this role?

The wage schedule ranges from $31.500 to $42.230 per hour.

What are some of the key responsibilities of the Clinical Research Coordinator I?

Key responsibilities include consenting participants, preparing clinical research documentation, screening for eligible study participants, performing data entry, and maintaining compliance with research ethics.

What qualifications are required for this position?

Candidates should have 2 years of experience as a research coordinator in clinical trials, current Good Clinical Practice (GCP) knowledge, completion of a recognized clinical trials/research education program, and knowledge of medical terminology, among others.

Is experience with ethics boards necessary for this job?

Yes, demonstrated knowledge of Research Ethics Board requirements for research is required.

Are there any travel requirements for this position?

Yes, travel to regional sites may be required.

What are the conditions of employment?

Terms and conditions of employment are in accordance with Lakeridge Health's policies and procedures.

Is a background check required for new applicants?

Yes, successful external applicants must provide a satisfactory Criminal Investigation Reference for the vulnerable sector, dated within the past six months.

Does Lakeridge Health accommodate applicants with disabilities?

Yes, accommodations will be provided in all parts of the recruitment and assessment process in accordance with the Accessibility for Ontarians with Disabilities Act (AODA).

Are COVID-19 vaccinations required for new hires?

Yes, new Lakeridge Health team members will be required to provide proof of full vaccination for COVID-19 during their Post-offer/Pre-employment Health Assessment, subject to exemptions recognized under the Ontario Human Rights Code.

Lakeridge Health is a healthcare system serving communities in Durham Region and beyond. #OneSystemBestHealth

Science & Healthcare
Industry
5001-10,000
Employees
1998
Founded Year

Mission & Purpose

Lakeridge Health is a healthcare provider that operates multiple hospitals and medical facilities, offering a wide range of health services, including acute care, rehabilitation, mental health services, and cancer treatment. Their ultimate mission is to provide high-quality, patient-centred healthcare to the communities they serve. Lakeridge Health's purpose is to enhance the health and well-being of their patients by delivering compassionate, innovative, and accessible healthcare services, while continually striving for excellence in clinical practice and patient care.