Site Care Partner I/II - FSP
Türkiye, Remote Job ID R0000029518 Category Clinical Trials Date Posted 11/18/2024Overview
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
We are inviting applications to join our Turkey CRA team.
Home-based Site Care Partner I or II.
Permanent, full-time.
The role is open to candidates with Lead or Senior CRA experience only.
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 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 (SCP ) 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 closing 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.
We offer exceptional financial rewards, training, and development. Expect exciting professional challenges but with a healthy work/life balance. We value your welfare just as highly as that of our patients.
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#LI-REMOTE
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.
- APEX CRA
- CRA I
- CRA II
- Senior CRA
- Project ManagementSubject Matter ExpertPeople Management
Employee Insights
TEAM IMPRESSIONS
Why Clinical Research Associates work at Parexel
