Clinical Research Coordinator - Vancouver, Canada - Medspa Partners

Medspa Partners

Verified Company

Vancouver, Canada

1 week ago

Posted by:

Sophia Lee

beBee Recruiter

Description

Clinical Research Coordinator

Part Time or Full Time

Responsibilities:

Design and implement study tools to monitor and track administrative and clinical activities including but not limited to the following: spreadsheets, databases, source documentation, educational materials and other duties as determined by the Team Lead.
Perform data abstraction and data entry.
Travel to Investigator Meetings as required.
Liaise with physicians, nursing, and laboratory staff, as well as industry representatives.
Ensures that clinical monitoring activities of their assigned team are performed to the Sponsor's satisfaction and in accordance with applicable standard operating procedures (SOPs), regulations, good clinical practices, and studyspecific requirements.
Strong Standard Operating Procedures (SOPs) execution
CTMS experience is an asset.
Keeps Team Lead and PI apprised and informed of all situations and daily operations.
Escalates problems swiftly to appropriate parties; Team Lead, PI, Sub-I, and Monitor when applicable.
Communicate with sponsors and their representatives as well as monitoring agencies or third parties in a respectful manner to schedule and complete tasks.
Assist in planning and organizing of clinical trial startups including feasibility review, submissions when required.
Strong background in clinical research regulatory requirements
Collaborates and implements methodologies, policies, procedures, and standards in clinical research protocol management to ensure quality data including CAPA & ALCOA
Advises key members on internal Quality Control (QC) findings and ways to continually improve.
Regularly meets deadlines related to individual as well as team performance on projects/assignments.
Support audit preparation for any site inspections
Abide by and advise site on Good Clinical Practice (GCP), standard Operating Procedures (SOPs), company guidelines, and local healthcare and privacy regulations.
Manage protocolspecific recruitment targets and support efforts to achieve site/company KPIs.
Interact with investigators, and delegated team members and thirdparty vendors for successful study execution.

Qualifications:

A Bachelor of Science, and/or a level of education, training, and experience equivalent to a Bachelor's degree in a science discipline or related field such as Health Administration, Nursing, Microbiology, or Business Administration.
Minimum of two years' experience seeing patients.
Minimum of two years' experience in clinical research
Experience in a dermatology clinical setting is preferred and knowledge of medical terminology is required.
A proven professional and tireless work ethic will be an asset in managing multiple projects with hard deadlines.
A demonstrated ability to act as a member of an interdisciplinary team to plan, organize, implement, trouble shoot and coordinate research projects in a timely and efficient manner.
An ability to communicate effectively and work independently is critical, as well as the ability to organize and prioritize workload.
Other qualities that will be considered are attendance record, grooming, and temperament.
CCRC qualified; GCP and Health Canada Division 5 certified; IATA certified.
Phlebotomy Certification is an asset.

This role will be perfect for you if:

You are a Clinical Research Coordinator with at least two years' experience on sponsor directed patient-facing clinical trials.
You are a clinical research professional with a passion for producing the highest quality of research data a
You thrive working in a dynamic clinical research environment.

Job Types:
Full-time, Part-time

Salary:
$25.00-$30.00 per hour

Application question(s):