Clinical Research Associate

3 weeks ago

Québec, Quebec, Canada Parexel Full time

Clinical Monitoring and Compliance Specialist

**Job Summary:**

We are seeking a highly skilled Clinical Monitoring and Compliance Specialist to join our team at Parexel. As a Clinical Monitoring and Compliance Specialist, you will be responsible for ensuring the integrity and quality of clinical data, as well as ensuring compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines.

**Key Responsibilities:**

* Conduct on-site and remote monitoring activities to ensure compliance with study protocols and regulatory requirements
* Verify the accuracy and completeness of clinical data and ensure that it is in compliance with GCP guidelines
* Identify and report any deviations or issues related to clinical data or study conduct
* Collaborate with site staff and other stakeholders to ensure that study protocols are followed and that data is accurate and complete
* Provide guidance and training to site staff on GCP guidelines and regulatory requirements

**Requirements:**

* Bachelor's degree or equivalent in a related field
* Minimum of 1 year of experience in clinical monitoring or a related field
* Strong knowledge of GCP guidelines and regulatory requirements
* Excellent communication and interpersonal skills
* Ability to work independently and as part of a team

**What We Offer:**

* Competitive salary and benefits package
* Opportunities for professional growth and development
* Collaborative and dynamic work environment

**How to Apply:**

If you are a motivated and detail-oriented individual with a passion for clinical research, please submit your application, including your resume and a cover letter, to [insert contact information].

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