Clinical Research Associate Ii
5 months ago
Clinical Research Associate II
Remote - Canada
Phase IV Registries - Rare Disease
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
Why settle for one thing when you can have everything? Fortrea gives you the best two for one opportunity for career growth. Who doesn’t want twice the perks - working at one of the largest FSP CROs—and partnering with one sponsor with a dedicated therapeutic focus.
We are seeking a Clinical Research Associate II to be responsible for all aspects of study site monitoring and management including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned.
- Additional responsibilities include:
- Organize and make presentations at Investigator Meetings-
- Participate in the development of protocols and Case Report Forms and Clinical Trial Reports as assigned-
- Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks as instructed by supervisor as assigned-
- Negotiate study budgets with potential investigators and assist the Covance legal department with statements of agreements as assigned-
- Independently perform CRF review; query generation and resolution against established data review guidelines on Covance or client data management systems as assigned by management-
- Travel, including air travel, may be required and is an essential function of the job-
- Prepare accurate and timely trip reports-
- Review progress of projects and initiate appropriate actions to achieve target objectives**Requirements**:
- University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure). An equivalent amount of experience can be substituted as appropriate.-
- Minimum of at least 1 year of Onsite Clinical Monitoring experience along with at least 1 year total in clinical research experience is required.-
- Phase IV Registry and/or Rare Disease experience preferred but not required.-
- French Language proficiency preferred, but not required.-
- Valid Driver's License-
- Thorough knowledge of ICH Guidelines and understanding of local regulatory requirements-
- Thorough knowledge of monitoring procedures; Basic understanding of the drug accountability process-
- Have a full understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs-
- Good planning, organization and problem-solving abilities; Ability to work with mínimal supervision-
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- .- Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit- .- Fortrea is proud to be an Equal Opportunity Employer:
- As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply. For more information about how we collect and store your personal data, please see our Privacy Statement._
- #LI-RemoteFortrea is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, mar
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