Opportunity
Join our Talent Pool - Clinical Research Associates (Eastern Europe)
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About the role
Talent pool for anticipated Clinical Research Associate roles supporting a Clinical Monitoring team across Budapest, Vienna, Zagreb, and Vilnius. Full-time permanent remote work is listed, with multiple seniority levels from CRA I to Senior CRA. Duties include site monitoring, data review, safety follow-up, startup and activation, TMF documentation, and possible mentoring or lead responsibilities. This is not necessarily an immediate active vacancy.
Key requirements
Employer-stated requirements where available.
- • CRA I - minimum 1 year experience + Honours Bachelor Degree CRA II - Minimum 2 years experience + Honours Bachelor Degree Sr. CRA - Minimum 3 years experience + Honours Bachelor Degree
- • At least 1 year of relevant experience
- • Required skills: Site management, Remote and onsite monitoring visits, Clinical trial data and system review, Query resolution, Safety review and adverse event follow-up, Site startup and activation, Trial material delivery, Recruitment support, TMF documentation, GCP compliance, SOP compliance
Opportunity details
- • Workplace: Remote
- • Employment: Permanent
- • Posted: Mar 3, 2026
- • Original advert language: English
Full vacancy
Read the employer’s full description
Job title: Join our Talent Pool - Clinical Research Associates (Eastern Europe)
Team: General - Talent Pools
Location: Budapest
All locations: Budapest, Vienna, Zagreb, Vilnius
Work type: Full-time, Permanent
Workplace type: remote
Don't see an opening that quite matches what you're looking for, or not ready to make a move yet? Let us know!
We are proactively inviting qualified candidates to join our talent pool for anticipated Clinical Research Associate needs (across multiple seniority levels) to support our Clinical Monitoring team.
What the process looks like:
A Talent Acquisition representative will contact selected candidates to schedule a qualifying call to learn more about your experience, and what your timeline looks like
We'll also share details about timelines on our side - note that this Talent Pool is not necessarily for an immediate, active role
We'll keep your details on file and in mind - if an active vacancy does arise which matches your seniority and logistical details, we'll reach out to get an interview scheduled with the team
About the Role(s)
Clinical Research Associate I/II
Support/conduct (as appropriate) site management through remote and supervised onsite visits (initiation, monitoring, and close-out) in compliance with SOPs, protocol, and GCP.
Perform remote data and system reviews (EDC, CTMS, RBM, TMF) to ensure data quality, completeness, and regulatory compliance.
Assist/lead (as appropriate) with query resolution, safety reviews, and adverse event follow-up throughout the study lifecycle.
Support/conduct (as appropriate) site startup and activation activities, including investigator coordination, trial material delivery, and recruitment support.
Maintain accurate, timely, and complete TMF documentation, requesting updates as required.
Provide day-to-day operational support to Senior CRA, and Lead CRAs.
Participate in training, study meetings, and CRA development activities, building competencies required for role progression.
Sr. Clinical Research Associate
As above, with the addition of the following:
Act as subject matter expert, mentor, coach and/or provide performance feedback to manager for peers.
Assist with selection, hiring, training, and supervision of CRAs as needed. Perform co-monitoring and training visits with CRAs.
When required, act as the first escalation point for the resolution of site/patient issues or to address Sponsor concerns.
May represent Director, Monitoring and Site Management or Manager, Clinical Site Management in BD initiatives with a site monitoring focus.
May be assigned Lead CRA role and manage monitoring services for a group of projects and/or CRAs on large/complex project(s) including directing/guiding day to day activities and review/approval of monitoring reports.
Oversee overall integrity of the study to promote positive working relationships with the site and staff.
Ensure SOPs in place to optimize patient recruitment providing guidance to site teams of inclusion/exclusion criteria.
Qualifications (may vary depending on role needs)
CRA I - minimum 1 year experience + Honours Bachelor Degree
CRA II - Minimum 2 years experience + Honours Bachelor Degree
Sr. CRA - Minimum 3 years experience + Honours Bachelor Degree
Compensation/Total Rewards
Compensation may vary depending on the role seniority, geographic location, and candidate experience.
All full-time, permanent roles will include a base salary + elgibility for performance-based bonus, as well as a variety of health, dental, RRSP matching, and more!
If contacted for an initial call, a member of our TA team will be happy to share more.
Stay Alert to Recruitment Scams
We have been made aware of individuals posing as our recruiters and contacting candidates with fraudulent opportunities. Our hiring process always includes direct engagement with a recruiter or hiring manager, and we will never ask for sensitive personal information early in the process. Official communication will only come from our company email domains. If something doesn’t feel right, we encourage you to verify before responding.
HealthRoleIQ summarises the verified facts needed for matching. Complete responsibilities, project background and employer benefits remain available on the original employer posting.
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- Last verified: Sep 15, 2026