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.
For our Istanbul office, we are currently looking for an Associate Clinical Study Director.
An ACSD will be dedicated to a single sponsor in BioPharma, who is revolutionizing healthcare by harnessing the power of science to benefit people, society, and the planet. ACSD will be employment on a permanent basis, receive a highly competitive base salary combined with an excellent benefits package. They will also receive numerous financial incentives throughout the year. For dedicated Individuals we offer a career path within Parexel, world-class trainings and professional challenges. At the same time, we offer a healthy work-life balance valuing our employees’ welfare just as highly as that of our Patients.
As an Associate Study Director, you will lead Local Study Teams at the country level to deliver clinical studies according to agreed resources, budget, and timelines complying with procedural documents, international guidelines, and relevant local regulations.
You will be responsible for ensuring that sites are identified, site qualifications performed, set up, initiated, monitored, closed and documentation archived.
We expect the applicants to be hold a Bachelor’s degree in life science, have at least 1 year experience as a Clinical Trial Leader or Project leader and minimum 3 years of experience in Development Operations (CRA, SCRA) or other related fields (Medical Affairs-led or Academic-led studies).
Our Talent Acquisition Team can answer any additional questions about the role or Parexel.
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What We Do
Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com. Community Guidelines Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are: • Abusive, harassing or threatening to others. • Defamatory, offensive, obscene, vulgar or depicting violence. • Hateful targeting by race/ethnicity, age, color, creed, religion, gender, sexual preference or orientation, nationality or political beliefs. • Sexually explicit or pornographic. • Fraudulent, deceptive, libelous, misleading or unlawful. • Referencing criminal or illegal activity. • Spamming. We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.
