• We use cookies to help make our website work. LEARN MORE

Clinical Research Associate

Czech Republic   •  €0 per annum  •  Permanent, Full time


An excellent opportunity has arrisen for an experineced or entry level CRA to join my client, a full-service CRO based in Prague. Within this role you will provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries and join their mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. Therapeutic areas include; oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. 
 
Responsibilities:

Our successful Clinical Research Associates possess varied backgrounds in medical and other science-related healthcare fields.  Individuals who have succeeded in the CRA role include:

  • Nurses
  • Dieticians
  • Pharmacy Technicians
  • Pharmaceutical/Device Sales Representatives
  • Biotech Engineers
  • PhD/Pharm.D candidates
  • Health and Wellness Coordinators
  • Research Assistants

UNEXPECTED REWARDS
 
This role takes you on a journey through travel and excitement which will allow you to make a difference on a large scale through the enhancement of pharmaceuticals and medical devices.  The CRA position provides many other distinctive advantages including:

  • Dynamic working environment, with varying responsibilities day-to day
  • Expansive experience in multiple therapeutic areas
  • Work within a team of therapeutic and regulatory experts
  • Defined CRA promotion and growth ladder with potential for mentoring and management advancements
  • Competitive pay and opportunity for significant travel bonus

DESCRIPTION OF JOB DUTIES
 
As a CRA, you will specifically be responsible for the following:

  • Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol;
  • Communication with the medical site staff including coordinators, clinical research physicians and their site staff;
  • Verifying adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;
  • Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating  protocol deviations appropriately per SOPs, GCP and applicable regulatory requirements;
  • Verification that the investigator is enrolling only eligible subjects;
  • Regulatory document review;
  • Medical device and/or investigational product/drug accountability and inventory;
  • Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;
  • Assessing the clinical research site?s patient recruitment and retention success and offering suggestions for improvement;
  • Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies,  and recommended actions to secure compliance. 

 
Qualifications:

  • Minimum of a bachelor?s degree;  Health or life science related field preferred;
  • Fluent English & Czech;
  • Willing to travel approximately 60% nationally;
  • Familiarity with Microsoft® Office; and
  • Strong communication and presentation skills a plus.
  • Job location: Prague, Czech Republic

For further details, please contact Tim Barratt on +44(0)1727 817 626 or email tbarratt@achieva.co.uk

  • Agency: Achieva Group Limited
  • Reference: BH-34229
  • Posted: 6th January 2023
  • Expires: 3rd February 2023

Achieva Group Limited

Share this job: