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Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.
Regional Site Start Up II - FSP
Job ID R0000043254Parexel FSP is looking for Regional Site Start Up II to join our team in US or 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 escalate 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.
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