Site Activation Partner I - FSP (Fixed-Term 7 months)

Résumé du poste

The Site Activation Partner is responsible for managing operational activities from study start-up to close-out, ensuring compliance with regulatory standards and study timelines. They coordinate essential document management, facilitate ethics committee submissions, and provide ongoing support to investigator sites throughout the clinical trial lifecycle.

Détails du poste

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Parexel FSP is looking for Site Activation Partners to join our team. Candidates must have at least 2 years of start-up experience and experience with US/CAN. This is a 7-month temporary assignment with the potential to transition into a full-time role. Job Overview: The Site Activation Partner I (SAP I) is responsible for leading or supporting operational activities from start up to close out, for assigned studies and investigator sites to ensure compliance with study timelines and in accordance with prevailing laws, Good Clinical Practices, and client standards. Responsibility within a country and may span over more than 1 country depending on the geographical region and business needs. Key Accountabilities: Clinical Trial Site Activation: Initiate and coordinate activities and essential documents management during start up towards the compilation of a high quality Investigator Initiation Package (IIP) leading to approval for site initiation Provide support to resolve issues or concerns and timely escalation of site issues where applicable Prepare, validate and submit regulatory documents such as completed IIP, Institutional Review Board (IRB) approval forms, FDA 1572/Attestation Form, for internal regulatory approval within required timelines Manage and coordinate with other supporting roles to ensure timely site activation and operational activities Support the compilation of the Central Investigator Review Board package and submissions to approval of the study (where applicable) and other committees as per country requirements Coordinate the timely communication, documentation and responses between client and central ethics committee to bring clinical study to approval (country dependent) Support investigators sites with local IRB workflow from preparation, submission through approval Assist with the preparation, handling, and distribution of clinical documentation and reports according to the scope of work and standard operating procedures Support and implement activities in Shared Investigator Platform (SIP) to align with the client’s strategy as it relates to the role Clinical Trials Conduct: Post site activation, initiate and coordinate activities and essential documents management with the investigator’s sites towards the compilation of a high quality documents and updates through the life cycle of a study such as the documents management for protocol amendments, FDA 1572/Attestation revisions, ethics committee annual approvals and other activities required during study conduct Ensure maintenance of IRB/Ethics and other committees’ activities as applicable Responsible for timely filing of documents to Trial Master File (TMF) and assisting with periodic quality review of study files for accuracy and completeness Accurately update and maintain clinical trial systems that track site compliance and performance within project timelines Supports investigator sites, and study teams in preparation for and providing responses to site audits / inspections Communication: Maintain ongoing contact and communication with the study team and respond promptly to study team and investigator site requests Provide functional updates on a country and site level as required Establish tools for efficient updates to study team as needed regarding site status, issues, delays, approvals Disseminate central or local ethics approval to study team and Investigator sites where applicable Communicate local sites approvals to study team members and stakeholders Clinical Trial Site Support: As needed, perform, awareness session with site personnel on client requirements and to ensure ongoing compliance with study documentation in accordance with prevailing laws, Good Clinical Practices, and client standards Identify and resolve investigator site issues within required timeframes; align with study team and local country colleagues on corrective and preventative actions to close open issues and to prevent recurrence / persistence of issues Subject Matter Expert (SME): A good understanding of the site activation requirements and processes within the country/region and be able to learn and potentially implement in more than one country May be assigned as Site Activation Partner Point of Contact (PoC) on a study conducted in multiple countries May be assigned as an SME on a system and/or process, and represent the SAP function as applicable May represent the SAP role on global initiatives Able to act as an SME on projects and initiatives, as requested Support the mentoring of new hires on processes/ systems Compliance with Parexel standards: Complies with required training curriculum Completes timesheets accurately as required Submits expense reports as required Updates CV as required Maintains a working knowledge of and complies with Parexel processes, ICH-GCPs and other applicable requirements Skills: Knowledge of clinical research and development processes, key operational elements of a clinical trial, and ability to gain command of process details Understand the quality expectations and emphasis on right first time Compliance with all applicable company, regulatory and country requirements Attention to detail evident in a disciplined approach Ability to work independently and also as a team member Ability to organize tasks, time and priorities, ability to multi-task Understand basic medical terminology, GCP requirements and proficient in computer operations Ability to use and learn systems, and to use independently Microsoft Suite o Clinical Trial Management Systems (CTMS) Electronic Trial Master File o Electronic Investigator Site File (e.g. Florence) Document exchange portals o Shared Investigator Platform o Ethics, National Networks and Governing Bodies Portals and platforms (as needed) Flexible and adapt to off working hours in a global environment (when applicable) Able to travel as needed, including some international travel possible Knowledge and Experience: Experience working in the pharmaceutical industry/or CRO in study site activation preferred Knowledge of clinical trial methodologies, ICH/GCP, FDA and Global and local country regulations Must be fluent in local language and in English. Multilanguage capability is preferred Individuals based in Canada: Bilingualism (French, English) is preferred Effective verbal and written communication skills in relating to colleagues and associates both inside and outside of the organization Good technical skills and ability to learn and use multiple systems Education: School diploma or certificate with equivalent combination of education, training and experience or Bachelor of Science or Bachelor of Arts or equivalent Education in life sciences discipline is preferred Minimum 2 years relevant experience in clinical site management

Ce que vous ferez

The Site Activation Partner is responsible for managing operational activities from study start-up to close-out, ensuring compliance with regulatory standards and study timelines. They coordinate essential document management, facilitate ethics committee submissions, and provide ongoing support to investigator sites throughout the clinical trial lifecycle.

Exigences

Candidates must have at least 2 years of relevant experience in clinical site management and a strong understanding of ICH-GCP and regulatory requirements. Proficiency in English is required, with bilingualism in French preferred for candidates based in Canada.

Compétences indiquées

• Gestion du temps · Souhaitée
• Résolution de problèmes · Souhaitée
• Regulatory Compliance · Souhaitée
• Communication · Souhaitée

Autres compétences pertinentes

Relevées dans la description du poste. Confirmez les exigences importantes ci-dessus.

• Clinical research
• Site activation
• Regulatory compliance
• ICH-GCP
• FDA regulations
• Investigator site management
• Document management
• Clinical trial management systems
• Trial master file
• Ethics committee submissions
• Communication
• Problem solving
• Time management
• Medical terminology
• Microsoft suite
• Mentoring
• Standard Operating Procedure
• Mentorship
• Management
• English Language
• Workflow Management
• Detail Oriented
• Ethical Standards And Conduct
• Pharmaceuticals
• Consulting
• SAP Applications
• Pre-Clinical Development
• Auditing
• Multitasking
• Empathy
• Life Sciences
• Clinical Documentation
• Filing
• Institutional Review Board (IRB)
• Bilingual (French/English)
• Clinical Research
• Clinical Trials
• Corrective And Preventive Action (CAPA)
• Regulatory Documents
• Computer Operations
• Good Clinical Practices (GCP)
• Expense Reports
• Session Initiation Protocols
• Persistence
• Clinical Trial Management Systems
• Medical Terminology
• Trial Master File
• Electronic Trial Master File

Domaines d’emploi

• Healthcare
• Science & Research
• Consulting
• Site Activation Lead
• Clinical Trial Manager
• Research and Development Managers
• Clinical Research Coordinators
• Natural Sciences Managers