Regional Site Start Up II - FSP

Parexel; Canada; Remote; CAD 70,000 - 90,000; Full time

Job summary

Parexel is seeking a Regional Site Start Up II to lead site activation activities in Canada. You will manage timelines, document collection, and CTMS updates to ensure activation milestones are met and regulatory standards are followed.

You will work with US and Canada teams, translate documents when needed, and drive efficient cross-functional collaboration across clinical trial start-up processes.

Qualifications

• Bachelor’s Degree, minimum.
• 3 - 4 years of experience.
• Must have experience working with US and Canada.

Responsibilities

• Deliver site activation timelines for assigned sites.
• Collect and organize essential documents to meet regulatory requirements.
• Maintain site information in CTMS and ensure inspection readiness.
• Collaborate with internal and external stakeholders to ensure regulatory submissions meet local requirements.
• Translate essential documents as needed for submissions and approvals.

Skills

Interpersonal skills

Leadership

Data driven planning

Communication

Education

Bachelor's Degree

Tools

CTMS

TMF

MS Office

Job description

Parexel FSP is looking for Regional Site Start Up II to join our team in Canada.

Job Summary

The Regional Site Start Up (SSU) role is responsible for leading and delivering site start-up and activation activities across clinical trials. This role will ensure timely site activation, maintain strong relationships with sites, and work cross-functionally with internal and external teams to efficiently achieve study site activation timelines. The role provides regional expertise, ensuring large areas of geographic-specific needs are addressed and adherence to study milestone timelines. This role must possess excellent interpersonal skills, attention to detail, and the ability to collaborate across teams to ensure timelines are achieved.

CORE JOB RESPONSIBILITIES:

Site Start Up and Activation:

• Accountable to delivering individual site activation timelines to plan for assigned sites
• Gather, organize and share, as appropriate, all required essential documents from clinical sites and Sponsor specific documents to ensure compliance with Regulatory and Sponsor requirements as part of the site activation process
• Collect site intelligence to inform site discussions and maintain site information in CTMS
• Ensure site regulatory packages meet country requirements, TMF standards and ICH-GCP compliance
• Assist with reviewing Informed Consent Forms (ICF) as requested
• Facilitate the translation of Essential Documents that may be required in languages other than English for purposes of submission to and approval from Regulatory Health Authorities and/or Independent Review Board/Ethics Committees
• Provide regional expertise, addressing specific geographic challenges to facilitate site activation. Serve as the primary point of contact and escalation point for sites: troubleshoot issues and provide strategic solutions to ensure activation timelines are achieved
• Update trackers with key study information, risks and mitigation strategies
• Ensure all site start-up documents are filed in the TMF and are inspection ready
• Support inspection readiness activities related to site start up documents

Cross-Functional Collaboration:

• Partner with internal, external stakeholders and clinical sites to ensure good communication and coordination through the site start up phase
• Ensure alignment with all global and local regulatory requirements

Process Optimization and Compliance:

• Maintain accurate records of site activation progress, including updates on document collections, submissions statuses, and timelines
• Identify and elevate challenges or delays in document collection, regulatory submissions, or site activation processes for resolution
• Identify opportunities for process improvement in site start-up activities and implement best practices to enhance efficiency and effectiveness

Job Qualifications:

• Demonstrated interpersonal & leadership skills
• A data driven approach to planning, executing, and problem solving
• Effective communication skills via verbal, written and presentation abilities
• Proactive and self-disciplined, ability to meet deadlines, effective use of time, and prioritization Demonstrated vendor management experience
• Technical proficiency in trial management systems (CTMS, TMF) and MS applications including (but not limited to) Project, PowerPoint, Word, Excel Experience in the clinical drug development process, including study start-up
• Knowledge of ICH/GCP and regulatory guidelines/directives
• Ability to understand and implement operational strategic direction and guidance for respective clinical trials, fostering a culture of collaboration and trust across diverse teams and stakeholders.
• Support stakeholders by addressing concerns promptly and professionally, building positive relationships, and ensuring clear communication to maintain alignment with trial objectives
• Contribute to team productivity by maintaining open communication and supporting team members in their tasks
• Education: Bachelor’s Degree, minimum
• Years of Experience: 3 - 4 years
• Must have experience working with US and Canada.

#LI-REMOTE EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.