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Site Activation Partner I

Türkiye, Remote Job ID R0000020239 Category Clinical Trials Date Posted 02/17/2024
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As a Clinical Research Associate (CRA) at Parexel, you act as an integral part to get treatments to patients sooner. Our CRAs' priority is the safety and well-being of the patients. As you travel to investigator sites and perform your monitoring duties, we encourage you to be inquisitive, take accountability, build relationships, and act with integrity.

Join a team with a wide variety of experiences and knowledge, and work on global projects within a broad scope of therapeutic areas. We’re looking for people who want to grow personally and professionally and support their colleagues globally and cross-functionally.

Success Profile

Do you have these soft skills and interpersonal traits to succeed at Parexel?

  • Communicator
  • Detail-oriented
  • Flexible
  • Organized
  • Problem-solver
  • Self-starter

About This Role

Parexel FSP is currently hiring for a Site Activation Specialist on a

permanent, full-time basis.

This role is a match with Study Start Up Associate, Regulatory Affairs Specialist,

Regulatory Startup Specialist, Country Approval Specialist, Study Startup,

Site Activation Specialist, and Clinical Research Associate.

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 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 per 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.




Potential Career Path

Parexel offers various career paths and internal development programs for CRAs to advance to the next level. This could include enhancing your technical position, moving into management, or shifting to other areas of the business.

  • CRA I
  • CRA II
  • Senior CRA
  • Project Management
    Subject Matter Expert
    People Management

Employee Insights


Female employee leaning on desk with Parexel logo in background Team photo
Larger team photo
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Team outing at laser tag Male employee with medical mask on sitting at desk with laptop open Team photo in an office setting

Why Clinical Research Associates work at Parexel

Learn About Our Culture

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