Site Care Partner - Istanbul - FSP

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.

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.

Job Purpose: The Site Care Partner I (SCP I) is the “face of the client” and therefore accountable for:

• Ensuring that sites receive necessary support and engagement issues are resolved.

• Being the main client's point of contact for investigative sites and accountable for site start-up activities through activation, building, and retaining investigator site relationships.

• Providing support from site recommendation through the lifecycle of studies

• Site-level recruitment and operational success.

• Safeguarding the quality and patient safety at the investigator site.

• Contributing to country and site selection activities by proactively collaborating with key stakeholders and providing local intelligence to country outreach surveys, investigator strategies, and client pipeline opportunities under supervision.

Experience required:

• Demonstrated experience in site management with prior experience as a Clinical Research Associate or Lead CRA.

• Demonstrated experience in startup activities through site activation.

• Demonstrated experience in conducting and close-out activities.

• Demonstrated knowledge of quality and regulatory requirements in applicable countries

• Able to Identify and build effective relationships with investigator site staff and other stakeholders.

• Proficiency in local language preferred.

• English proficiency.

• Ability to manage travel as required.