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კლინიკური კვლევის თანაშემწე
თარიღები:
20 ნოე - 19 დეკ
ელ.ფოსტა გამოხმაურებისთვის: velichka.duncheva@comac-medical.com
მდებარეობა:
თბილისი
კატეგორიები:
სამედიცინო 
ქვეკატეგორიები:
სხვა (სამედიცინო)
დასაქმების ფორმა:
სრული განაკვეთი
ენები:
ინგლისური
განათლება:
ბაკალავრი
აღწერა:
Great job opportunity for a CLINICAL RESEARCH ASSOCIATE for one of the most reputable, full-service providers of CRO and SMO, COMAC MEDICAL,  with headquarter in Sofia, Bulgaria.

Established in 1997, with locations in Central & Eastern Europe and 290 full-time dedicated professionals, we are a recognized leader in clinical research and provide innovative and non-conventional solutions of high quality for the pharmaceutical industry.
Currently, we are looking for a professional to join our Georgian Team

What is expected to be done?
  • Conducts feasibility studies and site qualification visits;
  • Develops and ensures strong site relationships through all phases of the trial;
  • Gains an in-depth understanding of the study protocol and related procedures;
  • Prepares study documentation e.g. draft protocols, and draft CRFs;
  • Collects, reviews, and monitors required regulatory documentation;
  • Communicates with Investigators and site staff on issues related to protocols;
  • Conducts recruitment, retention, protocol deviations, regulatory documentation, site audits/inspections and overall site performance;
  • Performs remote and on-site monitoring & oversight activities;
  • Identifies, assesses and resolves site performance, quality or compliance problems
  • Escalates if necessary, by following CRA Escalation Pathway in collaboration with CTL/CMM/PL;
  • Assists in planning and execution of Investigator Meetings or other study related meetings;
  • Assume additional responsibilities as required by Project Manager;

What is required for the role?
  • Graduate or postgraduate degree, preferably in the filed of Biology, Pharmacy, Chemistry or other relevant;
  • At least 3 years of experience as a Clinical Research Associate/Clinical Monitor;
  • Excellent knowledge of clinical research process;
  • Good knowledge of all functional areas of clinical trial management;
  • Working knowledge of current ICH/GCP guidelines and applicable country-specific regulations;
  • Excellent organizational, communication (verbal and written)
  • Positive attitude and ability to interact with various levels of personnel
  • Good analytical and problem-solving skills;
  • Ability to travel for site monitoring and/or co-monitoring activities, attend investigator meetings or vendor visits/audits, as required (up to 30%)
  • Ability to keep tight deadlines and work in a dynamic environment;
  • Working knowledge of Word, Excel, and Power Point
  • Fluency in English language

Why join Comac Medical?
  • Great team of knowledgeable, high-achieving and experienced professionals;
  • International and diverse work atmosphere;
  • Challenging projects in a different therapeutic area as well as in early phases;
  • Opportunity to enrich professional skills and progress in career development;
  • Competitive remuneration;
  • Professional trainings;

Core strengths of Comac Medical
  • Proven track record for quality and delivery;
  • Established and trusted relationships with KOLs;
  • Motivated, capable and dedicated team;
  • Global full-service capabilities;

If you are interested, challenged and convinced that the job opportunity is exactly for you, do not hesitate and send your detailed resume in English: velichka.duncheva@comac-medical.com Only the shortlisted candidates will be contacted in a timely manner.
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