Career

As a Clinical Research Associate (CRA), you will be an integral part of our global study team and will play a crucial role in our clients’ drug development processes. The ideal candidate for this position will possess energy, enthusiasm, excellent communication skills, exceptional time management skills, and a drive to achieve ambitious goals.

We are open to considering applicants with previous experience as CRAs who are ready to take the next step in their careers. The ideal candidate should have at least one-two years of successful monitoring experience.

Responsibilities:

• Plan, monitor, and coordinate clinical research study at trial sites in compliance with ICH GCP, SOPs, national legislation and standards, and instructions provided by the Sponsor
• Perform initial contact and participate in the assessment and selection of qualified investigators for inclusion in clinical programs
• Perform pre-selection, selection, initiation, interim monitoring, and closeout site visits, and ensure data standards are met
• Manage data collected from clinical sites, including diagnostic images, and resolve data queries
• Review informed consent forms
• Assist in the coordination of investigator meetings

Requirements:

• – University degree in Medicine or Pharmacy
• Fluency in English
• The ability to work hard as a member of a team, travel, communicate effectively, learn, and share knowledge is expected from our employees

We are seeking a Clinical Trial Assistant (CTA) for a position in Tbilisi, Georgia. The CTA will be responsible for helping the Project Manager and Clinical Research Associate by managing both paper and electronic documents related to clinical trials. This includes administrative tasks related to study start, regulatory submissions, study run, and close-out processes. The CTA will ensure that all activities are in line with GCP, SOPs, and local regulations.

To qualify for this role, applicants must have a BA degree in Medicine or Pharmacy, as well as a good command of the English language (both written and spoken). Georgian should be the candidate’s native language. We welcome applicants who are either new graduates or have more experience.

Responsibilities for this position include:

• reviewing documents,
• assisting with generating and reconciling queries to investigative sites/clients to resolve problem data,
• managing study supplies, and organizing shipments,
• creating, updating, tracking, and maintain study-specific trial management files, tools, and systems
• assisting local project team members with other administrative activities as needed (such as payments to investigators, correspondence with clients, preparation of status reports, and organization of investigators’ meetings).

We are looking for a Clinical Trial Assistant (CTA) in Budapest, Hungary.

The role of CTA is to support the Project Manager and Clinical Research Associate. CTA performs the management of paper and electronic documents related to clinical trials. Administrative tasks related to study start, regulatory submissions, study run, and close-out process. Ensures that activities are in line with GCP, SOPs, and regulations.

The following skills/experience is required: Education – BA/BS degree, natural sciences including teachers. Good command of written and spoken English language. Hungarian as the native language. New graduates or anyone more experienced are welcome.