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Study Operations Manager I ( FSP) Turkey

EXTRA HOLIDAYS - EXTRA PARENTAL LEAVE - FULLY FLEXIBLE
Remote: 
Full Remote
Contract: 
Experience: 
Mid-level (2-5 years)
Work from: 

Offer summary

Qualifications:

Minimum 2 + years leading clinical trials, Expertise in study and site dashboards, Experience in study start-up processes, Relevant operational clinical trial experience, Degree in a science-related field.

Key responsabilities:

  • Manage country-level activities for studies
  • Coordinate tasks within a study management team
  • Oversee study startup through close procedures
  • Utilize reporting tools for study oversight
  • Ensure compliance in quality management
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Parexel Pharmaceuticals XLarge http://www.parexel.com/
10001 Employees
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Job description

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Your missions

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.

We are inviting applications to join our EMEA Clinical Operations team as a

Study Operations Manager I/II, home-based.

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 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.

The Study Operations Manager I (SOM I) has 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 leading clinical trials is required.

  • Expertise in the use of study and site dashboards and reporting tools.

  • Experience in study start-up.

  • Comprehensive knowledge of own discipline with good knowledge of other disciplines ensures that the study can meet its goals and serve as a resource for others.

  • Comprehensive knowledge in managing and coordinating specific tasks and responsibilities as part of a larger study management team.

  • Demonstrated clinical research experience and/or study management/startup project manager experience.

  • Demonstrated experience in managing country-level operational activities and/or vendors.

  • Experience in study and quality management.

  • Experience working in a matrix management environment.

  • Relevant operational clinical trial experience

  • Education: degree or higher - preferably science-related.

  • Extensive oncology experience.

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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Required profile

Experience

Level of experience: Mid-level (2-5 years)
Industry :
Pharmaceuticals
Spoken language(s):
Check out the description to know which languages are mandatory.

Soft Skills

  • Analytical Thinking
  • Verbal Communication Skills
  • Team Management

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