Junior R&D Clinical Development Specialist

Pharmactive İlaç San. ve Tic. A.Ş.

Pharmactive Pharmaceuticals, established in 2010 with the understanding of "How Happy is the One Who Offers a Cure" is one of the largest generic pharmaceutical companies in our country and strives to bring hope to the patients in Turkey and throughout the world.

 We believe that our team is the most valued resource for our success and we can build a better future together. We invite you to be a part of this team in Pharmactive R&D Directorate as Junior R&D Clinical Development Specialist.

Would you like to be a member of this team that is shaping the future?

 QUALIFICATIONS AND SKILLS

·        Bachelor’s degree in Pharmacy, Bioengineering, Molecular Biology and Genetics, Chemical Engineering, Biology or Chemistry

·        Newly graduate, post graduate, preferably PhD graduate or at least 1 year of experience in a relevant field

·        Proficiency in MS Excel, PowerPoint and Word. 

·        Excellent command of English (written and spoken)

·        Strong communications skills and good at teamwork

·        Ability to perform good and efficient reporting

·        Has no obstacle to domestic and foreign travel

·        Located in/ able to locate in Çerkezköy, Kapaklı, Saray, Çorlu, Ergene, Avcılar, Beylikdüzü, Büyükçekmece, Lüleburgaz

·        No military obligation for male candidates

 JOB DESCRIPTION      

 ·        Planning, following up and control of Bioequivalence / Bioavailability study processes

·        Performing Bioequivalence / Bioavailability literature studies related to the projects

·        Preparing of Bioequivalence / Bioavailability protocols and making necessary applications for starting, carrying out and terminating clinical studies and following the process

·        Preparation, distribution, filing and archiving of documentation related to Bioequivalence / Bioavailability studies

·        Performing periodical checks of study files and ensuring their accuracy,

·        Evaluation of the final reports of the completed Bioequivalence / Bioavailability studies and submission to the competent authorities,

·        Preparing documents in CTD format for drug registration applications