Offer summary

Qualifications:

Minimum of 2+ years of clinical trial management experience in CRO, Pharma, or Biotech., Experience in study startup and full lifecycle of clinical trials., Knowledge of IRB/EC submissions and vendor management in Turkey., Degree or higher in a science-related field..

Key responsabilities:

Manage study-specific country-level activities from startup to close for studies of limited complexity.

Oversee operational activities and ensure compliance with regulatory requirements.

Utilize study and site dashboards for reporting and performance tracking.

Collaborate with vendors and stakeholders to facilitate smooth trial operations.

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 a home-based Study Operations Manager
position. Permanent, full-time.

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.

The Study Operations Manager I (SOM I) have responsibilities for study-specific country-level activities from study startup through conduct and study close on studies of limited complexity

Candidates with the following experience will be considered:
•   A minimum of 2 + years of clinical trial management experience as a Clinical Trial or Project Leader is required, gained in CRO, Pharma or Biotech.
•   Good recent study startup and experience in leading full lifecycle of clinical trial stages.
•   Essential to have SSU and trial management experience in Turkey.
•   IRB/EC submissions experience.
•   Vendor management experience managing country-level operational activities.
•   Expertise in the use of study and site dashboards and reporting tools.
•   Education: degree or higher - preferably science-related.

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.

Apply today!

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