Offer summary

Qualifications:

Experience in study activation and/or site management in a pharmaceutical, biotechnology, or CRO environment., Knowledge of global and local regulatory requirements and EC submissions., Understanding of key operational elements of clinical trials, including study start-up and close-out activities., Fluency in English and the local language is required..

Key responsabilities:

Lead or support operational activities from study start-up to close-out for assigned studies and investigator sites.

Ensure compliance with study timelines and regulatory standards.

Collaborate with clients to meet their needs and expectations throughout the study process.

Maintain adherence to Good Clinical Practices and client standards.

Job description

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 currently hiring for a Site Activation Specialist on a permanent,
full-time and homebased basis.

This role is a match with Study Start Up Associate, Regulatory Affairs Specialist, Regulatory Startup Specialist, Country Approval Specialist, Study Start-up and Site activation Specialist and Clinical Research associate experience.

Single sponsor dedicated to a worldwide biopharmaceutical company that relentlessly seeks breakthroughs to improve patients’ lives. Their daily innovation contributes to a healthier global community. This is the space where today’s

visionaries, solution-seekers, and trailblazers converge to shape tomorrow’s groundbreaking solutions. Together, we have the power to revolutionize patients’ well-being. Every choice we make and every step we take is guided by our unwavering focus on patients, fostering an environment where innovation thrives.

Position Purpose:
The Site Activation Partner (SAP ) 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.

Skills and Education:
•   Experience in study activation and/or site management from a pharmaceutical/biotechnology or CRO environment.
•   EC submissions experience
•   Demonstrated knowledge of global and local regulatory requirements
•   Demonstrated understanding of key operational elements of a clinical trial (e.g., study start-up, conduct, close-out activities, reporting.
•   Fluent in English and local language.

For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is the CRO trusted by life sciences companies to innovate, keeping patients at the center of everything we do, and where an inclusive global community helps you be your best, transforming any career into a life-changing achievement.

APPLY TODAY!

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