Clinical Trial Coordinator

4 days ago

Edmonton, Canada Stratica Dermatology Full time

**PURPOSE**

**CLINICAL TRIAL COORDINATOR RESPONSIBILITIES**
- Assist in the planning, initiation, and execution of clinical trials.
- Coordinate participant recruitment, screening, and enrollment according to study protocols.
- Administer drug to trial patients following trial protocol and physician guidance.
- Schedule and conduct study visits under doctors’ guidance, ensuring compliance with study protocol.
- Coordinate with Probity Medical Research Inc for trial acquisition, patient recruitment efforts, and other ongoing support
- Represent Stratica Dermatology and physicians in a professional manner to pharmaceutical companies and physicians
- Work collectively with physicians, clinical trial staff, Clinic Manager, and nursing staff to have maximum patient enrollments into clinical trial studies
- Collect, record, and manage study data accurately and efficiently.
- Ensure data integrity and confidentiality.
- Assist with data entry and query resolution in clinical trial databases.
- Ensure all clinical trial activities adhere to Good Clinical Practice (GCP) guidelines, institutional policies, and regulatory requirements.
- Maintain regulatory binders and other essential documents
- Provide clear and concise information to participants regarding study procedures, risks, and benefits.
- Obtain informed consent from study participants.
- Monitor participant adherence to study protocols and follow up as needed.
- Address participant questions and concerns throughout the study.
- Organize and maintain clinical trial files and records.
- Coordinate meetings, teleconferences, and site visits.
- Assist in the preparation of study-related materials and presentations.
- Perform other administrative tasks as assigned by the Clinical Trials Manager.
- Perform other duties as requested by management and doctors

**Qualifications**
- Minimum 1 year experience in clinical research coordinator or related role (required)
- BSc or LPN diploma or higher from an accredited institution (required)
- Phlebotomy experience (preferred)
- ICH GCP, Health Canada Division 5 training (preferred)
- Current CPR certification valid within Alberta (preferred)
- Experience in dermatology (preferred)
- Knowledge of clinical trial methodology and regulatory requirements (preferred)
- Excellent organizational and time-management skills.
- Advanced self-initiated problem-solving skills.
- Strong attention to detail and accuracy.
- Proficient in Microsoft Office Suite (Word, Excel, PowerPoint).
- Ability to work independently and as part of a team.
- Effective written and verbal communication and interpersonal skills.
- Ability to handle confidential information with discretion.

**Schedule/Work Arrangement**
- This position is Monday-Thursday, 32/week
- Potential to increase to 40 hrs/week pending workload or to cover vacation.

If you possess the experience we are looking for, please submit your resume and cover lletter. Please note that only those selected for an interview will be contacted. We thank you in advance for considering Stratica Clinical Trials as your potential future employer

Expected hours: 32 per week

**Benefits**:

- Dental care
- Employee assistance program
- Extended health care
- Life insurance
- On-site parking
- Paid time off
- Store discount

Schedule:

- 8 hour shift

Application question(s):

- Do you have a minimum of an LPN License or a Bachelor of Science Degree?

**Experience**:

- Clinical Trials: 1 year (preferred)

**Language**:

- English (required)

Work Location: In person

  • Indigenous Clinical Trial Research Assistant

    2 weeks ago

    Edmonton, Canada University of Alberta Full time

    **Department** MED - Quality Management in Clinical Research **Salary range** $28.47 to $38.67 **Hours per week** 37.5 **Grade** 8 **Posted date** October 10, 2024 **Closing date** October 24, 2024 **Position Type** Full Time - Trust Funded **Description**: **_This position is a part of the Non-Academic Staff Association (NASA)._** This position has...

  • Clinical Research Coordinator

    2 weeks ago

    Edmonton, Canada Alberta Health Services Full time

    Your Opportunity: Description: As a Clinical Research Coordinator, you will provide support for research studies through the identification, collection, and reporting of clinical trial data. You will compile research, reports and regulatory documents as required by the protocol, and study/sponsor. This involves ensuring research information is timely,...

  • Clinical Research Coordinator

    1 day ago

    Edmonton, Canada University of Alberta Full time

    A leading university in Canada seeks a Research Coordinator - Respiratory Therapist to assist in managing clinical trials and research studies in the Division of Pulmonary Medicine. Applicants should be a Registered Respiratory Therapist with at least five years of clinical experience, preferably with patient education. This full-time role based in Edmonton...

  • Pulmonary Clinical Trials Coordinator

    1 day ago

    Edmonton, Canada The University of Alberta Full time

    A leading academic health institution in Edmonton is seeking a Research Coordinator to support clinical trials within the Division of Pulmonary Medicine. You will collaborate with researchers and healthcare professionals, ensuring high-quality study operations. Key responsibilities include patient recruitment, data collection, and maintaining regulatory...

  • Clinical Trial Project Lead

    2 weeks ago

    Edmonton, Canada University of Alberta Full time

    **Department** Faculty of Medicine & Dentistry - Medicine Dept **Salary range** $78,694.13 to $110,457.10 **Hours per week** 40 **Grade** 12 **Posted date** September 12, 2024 **Closing date** September 23, 2024 **Position Type** Full Time - Trust Funded **Description**: **_This position is a part of the Non-Academic Staff Association (NASA)._** This...

  • Administrative Support Ii

    4 days ago

    Edmonton, Canada Alberta Health Services Full time

    Your Opportunity: The Clinical Trials Assistant (CTA) is a multi-skilled position that supports various CTU staff including project managers, research nurses and coordinators within a team, or several teams, and is a key administrative liaison and support for several projects. Responsibilities include helping to organize and complete various regulatory...

  • Manager - Clinical Trials, Cancer Care Alberta

    2 weeks ago

    Edmonton, Canada Alberta Health Services Full time

    Your Opportunity:Are you looking to demonstrate your unique research and leadership experience to make a real difference in the fight against Cancer? Take your career to the next level and join Cancer Care Alberta (CCA) as we are currently searching for a Manager, Clinical Trials (MCT) to join our amazing team at the Cross Cancer Institute (CCI) in Edmonton....

  • Clinical Trials Lead in Emergency Medicine Research

    2 weeks ago

    Edmonton, Canada University of Alberta Full time

    A leading educational institution in Canada seeks a Research Nurse Coordinator to manage clinical trials and coordinate research under the supervision of a medical team. Applicants should hold an active Alberta nursing license and possess strong organizational and interpersonal skills. Responsibilities include managing HREB submissions, developing project...

  • Manager - Clinical Trials, Cancer Care Alberta

    2 weeks ago

    Edmonton, AB TG Z, Canada Alberta Health Services Full time

    Your Opportunity:Are you looking to demonstrate your unique research and leadership experience to make a real difference in the fight against Cancer? Take your career to the next level and join Cancer Care Alberta (CCA) as we are currently searching for a Manager, Clinical Trials (MCT) to join our amazing team at the Cross Cancer Institute (CCI) in Edmonton....

  • Clinical Research Coordinator

    1 week ago

    Edmonton, Canada Alberta Health Services Full time

    Your Opportunity: Description: As a Clinical Research Coordinator, you will provide support for research studies through the identification, collection, and reporting of clinical trial data. You will compile research, reports and regulatory documents as required by the protocol, and study/sponsor. This involves ensuring research information is timely,...