Careers

Currently we have the below detailed opened positions at HungaroTrial. If you wish to be the part of the most dynamic and fastest growing CRO company in Central and Eastern Europe, do not hesitate to apply to the position most appropriate for you.

Clinical Research Associate (CRA)

Location
Romania
Job details Hide details
Job Description

As a Clinical Research Associate you will be responsible for a variety of monitoring tasks and you will have a chance to work on clinical studies in different therapeutic indications, ensuring the clinical trial is conducted in compliance with study protocol and procedures, ICH-GCP guidelines and the applicable regulations and SOPs.

Main duties and responsibilities

  • Initiate, monitor and close-out clinical studies on study sites in accordance with applicable regulations, guidelines of ICH-GCP and standard operation procedures;
  • Prepare and perform regulatory and ethics submission (drug, medical device, non-interventional) for approval in accordance with applicable regulations, guidelines of ICH GCP and standard operation procedures of HungaroTrial (e.g. able to perform initial CA and EC submissions, amendment, notification, progress and safety report submissions, contract negotiations without direct supervision);
  • Support contracting procedure between Sponsor and Investigational sites;
  • Perform feasibilities and pre-study evaluations;
  • Document activity in accordance with ICH-GCP and standard operation procedures of HungaroTrial;
  • Prepare a summary (report) of activities as requested by the Manager.
Requirements
  • Bachelor degree in life sciences
  • 1 or 2 years experience in clinical research
  • Advanced level of English
  • Confident IT skills
  • Driver’s license
  • effective communication, customer focus, teamwork, time management, motivation to learn and develop

What we can offer:

  • Attractive and competitive salary
  • Dedicated and supportive team
  • Multinational environment
  • Regular team buildings and company events
Employment form
full-time

Clinical Trial Assistant (CTA)

Location
Romania
Job details Hide details
Job Description

Provide administrative support to clinical projects under direction of project manager and/or other designated clinical team members. Assist with general administrative functions as required.

MAIN DUTIES AND RESPONSIBILITIES

  • Provide administrative support for the project team members in clinical project related activities such as assistance in handling study documentation;  management of study files and/or clinical operations; regulatory activities; management of logistics.
  • Assist the preparation, collection, distribution, maintenance and retention of clinical documentation.
  • Assist the distribution of non-clinical supplies to trial sites.
  • Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
  • Contact with project team members, provide required reports, and regularly participate in project team communication and training.
  • Can be assigned also to non-clinical project related administrative activities such as office management and general administration.
Requirements
  • At least 2 years of working experience
  • Bachelor degree in life sciences
  • Advanced level of English
  • Confident IT skills
  • Flexibility
  • Teamwork
  • Accuracy, precision

 

WHAT WE CAN OFFER:

  • Competitive salary
  • Multinational environment
  • Regular team buildings and company events
Employment form
full-time employment

Clinical Research Associate (CRA)

Location
Serbia
Job details Hide details
Job Description

As a Clinical Research Associate you will be responsible for a variety of monitoring tasks and you will have a chance to work on clinical studies in different therapeutic indications, ensuring the clinical trial is conducted in compliance with study protocol and procedures, ICH-GCP guidelines and the applicable regulations and SOPs.

Main duties and responsibilities

  • Initiate, monitor and close-out clinical studies on study sites in accordance with applicable regulations, guidelines of ICH-GCP and standard operation procedures;
  • Prepare and perform regulatory and ethics submission (drug, medical device, non-interventional) for approval in accordance with applicable regulations, guidelines of ICH GCP and standard operation procedures of HungaroTrial (e.g. able to perform initial CA and EC submissions, amendment, notification, progress and safety report submissions, contract negotiations without direct supervision);
  • Support contracting procedure between Sponsor and Investigational sites;
  • Perform feasibilities and pre-study evaluations;
  • Document activity in accordance with ICH-GCP and standard operation procedures of HungaroTrial;
  • Prepare a summary (report) of activities as requested by the Manager.
Requirements
  • Bachelor degree in life sciences
  • at least 2 years (preferable more) experience in clinical research
  • Fluency in English and Serbian
  • Confident IT skills
  • Driver’s license
  • effective communication, customer focus, teamwork, time management, motivation to learn and develop

What we can offer:

  • Dedicated and supportive team
  • Multinational environment
  • Regular team buildings and company events
Employment form
full-time

Medical Monitor

Location
Hungary
Job details Hide details
Job Description
  • Provides therapeutic expertise as consultant for PM, CTL(s), CRA(s) and Investigators;
  • Attends Global training of investigators;
  • Communicates trends seen across regions or countries;
  • Participates in interim analysis trainings, DSMB meetings, pharmacovigilance discussions if requested;
  • Provides input for Final Study Report;
  • Integrates FAQs from across regions or countries;
  • Ensures safety and welfare of participating patients;
  • CRF data medical review and query;
  • Early recognition, identification, assessment and timely reporting of safety issues;
  • Provides 24/7 therapeutic expert consultation support to the sites;
  • Provides medical training for PMs, CTLs and CRAs;
  • Provides training in study specific medical issues for Investigators;
  • Provides assistance in interpretation of protocol;
  • Participates on initiation and monitoring visits if requested by CTL or PM;
  • Elaboration of Medical Monitoring- and Safety management Plans for clinical projects.
Requirements
  • Medical degree;
  • at least 2 years of experience in Medical Monitor position;
  • at least 3 years of clinical practice and at least 5 years of experience in clinical research as CRA or CRM;
  • Training in Medical Monitoring;
  • Confident IT skills and knowledge of IT systems;
  • Competency in written and spoken English.

What we can offer:

  • Attractive and competitive salary
  • Semi-home office opportunity
  • Cafeteria from the first whole month spent at the company
  • Dedicated and supportive team
  • Multinational environment
  • Regular team buildings and company events
Employment form
full-time

Clinical Trial Assistant (CTA)

Location
Hungary
Job details Hide details
Job Description

Provide administrative support to clinical projects under direction of project manager and/or other designated clinical team members. Assist with general administrative functions as required.

MAIN DUTIES AND RESPONSIBILITIES

  • Provide administrative support for the project team members in clinical project related activities such as assistance in handling study documentation;  management of study files and/or clinical operations; regulatory activities; management of logistics.
  • Assist the preparation, collection, distribution, maintenance and retention of clinical documentation.
  • Assist the distribution of non-clinical supplies to trial sites.
  • Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
  • Contact with project team members, provide required reports, and regularly participate in project team communication and training.
  • Can be assigned also to non-clinical project related administrative activities such as office management and general administration.
Requirements
  • Bachelor degree in life sciences
  • Advanced level of English
  • Confident IT skills
  • Flexibility
  • Teamwork
  • Accuracy, precision

 

WHAT WE CAN OFFER:

  • Competitive salary
  • Multinational environment
  • Regular team buildings and company events
Employment form
full-time employment