We are always looking for talented and motivated people to join our team. Apply today!
OCT is all about people. We do everything to create the perfect environment for our professionals to grow and develop along with the company. Take a look at the listed vacancies and send us your CV today. If you have not found what you have been looking for, send us a request to find out about job opportunities.
Project Manager (PM) is ultimately responsible for managing the clinical project within the set scope, time and budget and with the highest quality standards as agreed in the contract between the company and the client.
Main responsibilities include but are not limited to:
We are based in Saint Petersburg, Moscow and Kiev and are interested in finding full-time employees Salary is to be determined based on results of the interview
To apply please submit your resume and a cover letter to our Senior Training & Recruitment Manager Victoria Doilnitsyna, VDoilnitsyna@oct-clinicaltrials.com
This position presumes primarily responsibilities of monitoring (pre-study, initiation, routine, and close-out visits) of investigator sites for the compliance to the study protocol, ICH GCP, company’s SOPs and applicable regulations.The responsibilities will also include negotiations with the investigator sites of clinical trials agreements and study budgets, obtaining and review of required documents from investigator sites.
This position presumes full scope of monitoring responsibilities:
Experience in oncology trials will be an advantage!
Main responsibilities of Medical Writer include:
Clinical Trials Coordinator (CTC) coordinates the work of CRAs and provides assistance to Project Manager in clinical trials conduct.
* - Required fields