Create a Job Alert.

Enter your email below to save this search and receive job recommendations for similar positions.
Thank you. We'll send jobs matching these to
You already suscribed to this job alert.
CA
0 suggestions are available, use up and down arrow to navigate them
What job do you want?

Senior Clinical Research Associate job in Ottawa at MaxSys

Create Job Alert.

Get similar jobs sent to your email

Apply to this job.
Think you're the perfect candidate?
Senior Clinical Research Associate at MaxSys

Senior Clinical Research Associate

MaxSys Ottawa, Ontario Contractor


Senior Clinical Research Associate


Responsible for:
Ensures compliance with protocol and all regulatory policies, procedures and/or guidelines during clinical studies by training/guidance of investigators/study coordinators, and follow-up of corrective actions.
Ensures validity of study by identifying/resolving discrepancies and obtaining missing data and may track core lab activities and more complex components of the trial.

Contributes to developing and writing clinical protocols, case report forms, and other study aids for investigational products by addressing issues by interacting with appropriate personnel.

Maintains expertise in regulations for applicable geographies and types of studies (IDE, non¬ significant risk, feasibility, exempt, etc.). Serves as a resource related to clinical trial regulations.

May mentor and train new employees.

Serves as a trainer for contract research organizations (CROs) needed for additional monitoring support.

Ensures timely collection of study documentation by obtaining, maintaining and controlling all necessary records and documentation according to procedures and regulations.

Responsible for compliance with applicable Corporate and Divisional Policies and procedures.

Responsible for implementing the strategic initiatives established by the business and the department.

Responsible for tactical components of creating and driving customer-centric relationships cross-functionally to support product developments throughout the product(s) life cycle.

Subject matter expert (SME) in the technical application of product portfolio.

Execution of all aspects of testing including design, developing test materials, protocols, evaluation of test data, and all around support of analysis. Responsible for the execution of all aspects of clinical studies including but not limited to: site selection, pre-study visits, essential document review, site close-outs.

Other miscellaneous duties as may be required

Education & Experience
Require minimum 7 years relevant work experience or exposure to a technical / clinical environment, laboratory instrumentation and / or medical diagnostic testing.

Knowledge of lab practices or point of care testing environments, regulations and standards affecting medical diagnostics, lab practices, familiarity with statistics and statistical software (desired).

Bachelor’s degree or equivalent experience required; prefer background in the sciences or a medically-related area (such as but not limited to Biology, Chemistry, Nursing, Medical Technology, Respiratory Therapy or related field of study).

Excellent Communications skills, both oral and written.

Ability to initiate, plan and manage projects.

Strong decision-making skills and ability to prioritize.

Understands International Harmonized /Committee Good Clinical Practices, IHC/GCP.

Good Manufacturing Practice 21 CFR Part 820 is an asset.

Knowledge of project management tools and techniques.

Broad knowledge and application of business concepts, procedures and practices.

Advanced English Oral/Written.

Intermediate MS Office, SAS JMP.

Travel up to 30% of the time domestically and / or internationally may be required.

*if obtained outside of Canada/US must be verified by Agency*









#MST



#CB




 

Recommended Skills

Coherent Remote File System (Crfs)
Certified Radiology Administrator
Clinical Research Associate
Certified Retirement Administrator
Clinical Research
Documentation

Recommended Jobs

Senior Clinical Research Associate
MaxSys Ottawa Contractor
Radio Software Developer
Stefanini Ontario - Ottawa Full-Time Employee
$125k - $135k/year
Various General Labour Roles Available!
MaxSys Ontario - Ottawa Full-Time Employee
Apply to this job.
Think you're the perfect candidate?

Help us improve by providing feedback about this job:

Job ID: 26686

TIP

For your privacy and protection, when applying to a job online, never give your social security number to a prospective employer, provide credit card or bank account information, or perform any sort of monetary transaction. Learn more.

By applying to a job using you are agreeing to comply with and be subject to the Terms and Conditions for use of our website. To use our website, you must agree with the Terms and Conditions and both meet and comply with their provisions.