Site Activation Partner - site start up- FSP

Job summary

The Site Activation Partner leads operational activities from study start-up to close-out to ensure compliance with timelines and regulatory standards. They coordinate essential document management, support site initiation, and maintain clinical trial systems to track site performance.

Job details

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. The Site Activation Partner 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 sponsor standards. Other duties to include but not limited to: Initiate and coordinate activities and essential documents management towards the compilation of a high-quality Investigator Initiation Package (IIP) leading to approval for sites initiation Provide support to resolve issues or concerns and timely escalation of Site issues where applicable Manage and coordinate with other supporting roles to ensure timely site activation and operational activities Collaborate with in country regulatory group, and provide related/applicable site documents, as well as in countries where parallel submissions (Regulatory authority and ethics) are required Accurately update and maintain clinical trial systems that track site compliance and performance within project timelines Identify and resolve investigator site issues Experience required for this role: School diploma/certificate with equivalent combination of education, training and experience; BS/BA or bachelor’s degree in life sciences preferred Minimum 2 years relevant experience in Clinical Trials environment and clinical site activation. Experience working in the pharmaceutical industry/or CRO is an asset Knowledge of clinical trial methodologies, ICH/GCP, FDA and Global and local country regulations Must be fluent in Local language and in English. Multi-language capability is an asset #LI-LG4

What you’ll do

The Site Activation Partner leads operational activities from study start-up to close-out to ensure compliance with timelines and regulatory standards. They coordinate essential document management, support site initiation, and maintain clinical trial systems to track site performance.

Requirements

Candidates must have at least 2 years of relevant experience in clinical trials and site activation within the pharmaceutical or CRO industry. A bachelor's degree in life sciences is preferred, along with strong knowledge of ICH/GCP and global regulatory requirements.

Listed skills

• Regulatory Compliance · Preferred
• Project management · Preferred

Other relevant skills

Identified from the job description. Confirm important requirements above.

• Clinical Trials
• Site Activation
• Regulatory Compliance
• Good Clinical Practice
• ICH/GCP
• Investigator Initiation Package
• Clinical Trial Systems
• Project Management
• Stakeholder Coordination
• Regulatory Submissions
• FDA Regulations
• Life Sciences
• Empathy
• Ethical Standards And Conduct
• Management
• Pre-Clinical Development
• Consulting
• English Language
• Good Clinical Practices (GCP)
• Pharmaceuticals

Job areas

• Healthcare
• Science & Research
• Consulting
• Site Start-Up Specialist
• Clinical Trial Manager
• Research and Development Managers
• Clinical Research Coordinators
• Natural Sciences Managers