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Clinical Research Associates

Medex SMO

İlan yayından kaldırılmıştır!
Ankara, İstanbul(Avr.), İzmir, İstanbul(Asya)
İlan yayından kaldırılmıştır!

Job Type

Full-Time

Years of Experience

More than 1 years of experience

Department

Operations

Operations

Application Count

293 application

Job Type

Full-Time

Years of Experience

More than 1 years of experience

Application Count

293 application

Department

Operations

QUALIFICATIONS AND JOB DESCRIPTION

We are looking for Experienced Clinical Research Associates (CRA) with the following qualifications to take part in MEDEX's international projects.

 

Job Description:

  • Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit/contact reports.
  • Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines, while also ensuring compliance with the approved standard operating procedures (SOPs), protocol/amendment(s), GCP, and the applicable regulatory requirement(s).
  • Monitor the completeness and quality of Regulatory Documentation and perform site document verification.
  • Oversee integrity of the study and utilize problem-solving skills to promote rapport with the site and staff.
  • Review the performance of the trial at designated sites, ensure the rights and well-being of human subjects are safeguarded and are in accordance with protocol.
  • Evaluate the quality and integrity of the reported data, site efficacy and drug accountability.

 

Qualifications

More about you

On your first day we’ll expect you to have:

  • Min One Year Experience
  • Fluent in English
  • Bachelor’s or equivalent degree in biological science, chemistry, pharmacy or other health related discipline.
  • Residing in Ankara, Izmir and Istanbul
  • Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology.
  • Ability to perform all clinical monitoring activities independently.
  • Strong interpersonal, written, and verbal communication skills within a matrixed team.
  • Experience working in a self-driven capacity, with a sense of urgency and limited oversight.
  • A client-focused approach to work and flexible attitude with respect to assignments/new learning.
  • The ability to manage multiple tasks, evaluate a variety of unpredictable scenarios and achieve project timelines while being able to apply your understanding of study protocol(s).
  • An honest and ethical work approach to promote the development of life changing treatments for patients.
  • Strong computer skills, including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS) and MS-Office products such as Excel and Word.

Preferred Candidate

Bachelor’s(Graduate), Master’s(Graduate), Doctorate(Graduate)
English(Reading : Advanced, Writing : Advanced, Speaking : Advanced)

Klinik Araştırma Uzmanı pozisyonu ile ilgili daha detaylı bilgi almak ya da diğer iş fırsatlarını incelemek için aşağıdaki sayfaları inceleyebilirsiniz.

Klinik Araştırma Uzmanı Klinik Araştırma Uzmanı Maaşları Klinik Araştırma Uzmanı Nasıl Olunur? Klinik Araştırma Uzmanı Nedir? Klinik Araştırma Uzmanı İş İlanları
Medex SMO

Sağlık / Araştırma Hizmetleri 1+

Hakkımızda

MEDEX was builded in June 2013 as a unlimited company to provide site management organization services in Turkey. As the number of staff increases, It was converted to Limited Company in December 2015. Now, MEDEX providing Site Management Organisation services in whole over Turkey with 120 Study Site Coordinators. MEDEX is an organization that specializes in managing clinical research sites. We provide services for Contract Research Organizations (CRO’s), pharmaceutical companies, biotechnology companies, and medical device companies. Why MEDEX? Clinical trials frequently fail to reach its aim by reason of insufficient enrollment, poor compliance and performance. Proactive approach to site management is therefore a cornerstone of a clinical trial. Site Management Services from MEDEX take the burden off investigators so that they can focus on the patient, and ensure that the study is conducted at the highest standards of quality, ethics and performance. Our vision is to achieve extraordinary improvements in site management services. In pursuit of this, we support and provide the brightest minds in clinical research. Our primary mission is recruiting participants faster, executing more consistently and providing the highest quality data in the industry. Services: At MEDEX we work together to provide a comprehensive range of services. Our common purpose is to advance clinical research through speed, quality and reliability. Some of our services include; • Providing trained Study Coordinators, Study Nurses and Data Entry Personnel, • Project feasibility, IRB and EC submissions • Selling and renting calibrated Clinical Trials Equipments like fridge, refrigerator, sphygmomanometer, scale device. • Full CRO Services • Bioequivalence • Rental Services For Clinical Research Equipment’s ( 2-8 Refrigerator, -20 Freezer, -40/-60/-80 Ultradeep Freezer, Centrifuge, Incubator, Temperature Devices, Forehead Thermometer, IV Pump etc.) • Calibration Services for Clinical Research Devices • Data Management and Biostatistics • Physcical and Cloud Archiving • Study Supplies ( Filters, Syringes, Infusion Sets, urine dipstick, pregnancy test kits), Covid Test Kits) References: MEDEX bacame a qualified vendor of QuintilesIMS in Turkey in 2021. Our 120 site coordinators are in big cities of Turkey conducting QuintilesIMS responsible trials. MEDEX also supply site management organisation services to MSD Turkey, Pharm-Olam, Zeincro, Abbvie, Parexel, Roche and Quadro CRO.

MEDEX was builded in June 2013 as a unlimited company to provide site management organization services in Turkey. As the number of staff increases, It was converted to Limited Company in December 2015. Now, MEDEX providing Site Management Organisation services in whole over Turkey with 120 Study Site Coordinators. MEDEX is an organization that specializes in managing clinical research sites. We provide services for Contract Research Organizations (CRO’s), pharmaceutical companies, biotechnology companies, and medical device companies. Why MEDEX? Clinical trials frequently fail to reach its aim by reason of insufficient enrollment, poor compliance and performance. Proactive approach to site management is therefore a cornerstone of a clinical trial. Site Management Services from MEDEX take the burden off investigators so that they can focus on the patient, and ensure that the study is conducted at the highest standards of quality, ethics and performance. Our vision is to achieve extraordinary improvements in site management services. In pursuit of this, we support and provide the brightest minds in clinical research. Our primary mission is recruiting participants faster, executing more consistently and providing the highest quality data in the industry. Services: At MEDEX we work together to provide a comprehensive range of services. Our common purpose is to advance clinical research through speed, quality and reliability. Some of our services include; • Providing trained Study Coordinators, Study Nurses and Data Entry Personnel, • Project feasibility, IRB and EC submissions • Selling and renting calibrated Clinical Trials Equipments like fridge, refrigerator, sphygmomanometer, scale device. • Full CRO Services • Bioequivalence • Rental Services For Clinical Research Equipment’s ( 2-8 Refrigerator, -20 Freezer, -40/-60/-80 Ultradeep Freezer, Centrifuge, Incubator, Temperature Devices, Forehead Thermometer, IV Pump etc.) • Calibration Services for Clinical Research Devices • Data Management and Biostatistics • Physcical and Cloud Archiving • Study Supplies ( Filters, Syringes, Infusion Sets, urine dipstick, pregnancy test kits), Covid Test Kits) References: MEDEX bacame a qualified vendor of QuintilesIMS in Turkey in 2021. Our 120 site coordinators are in big cities of Turkey conducting QuintilesIMS responsible trials. MEDEX also supply site management organisation services to MSD Turkey, Pharm-Olam, Zeincro, Abbvie, Parexel, Roche and Quadro CRO.

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Yan Haklar

Yemek Kartı (Ticket, Multinet, Sodexo vb.), Yemekhane.

Klinik Araştırma Uzmanı pozisyonu ile ilgili daha detaylı bilgi almak ya da diğer iş fırsatlarını incelemek için aşağıdaki sayfaları inceleyebilirsiniz.

Klinik Araştırma Uzmanı Klinik Araştırma Uzmanı Maaşları Klinik Araştırma Uzmanı Nasıl Olunur? Klinik Araştırma Uzmanı Nedir? Klinik Araştırma Uzmanı İş İlanları