Start Up Associate in Estonia (freelance)
Other
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Quick Summary
Key Responsibilities
Perform and manage start-up activities for the assigned studies at country and site levels. Prepare, submit,
Requirements Summary
Perform and manage start-up activities for the assigned studies at country and
Technical Tools
Other
Responsibilities
~1 min read- →Perform and manage start-up activities for the assigned studies at country and site levels.
- →Prepare, submit, and track initial applications and amendments to Competent Authorities and Ethics Committees (CA/CEC/LEC) /IRBs and other bodies if applicable.
- →Manage official communication with Competent Authorities and Ethics Committees (CA/CEC/LEC) /IRBs and other bodies if applicable, prepare RFIs submissions packages to address authorities queries.
- →Advise study teams on local legislation from submission perspective, on import/export requirements;
- →Adapt trial materials (ICFs, labels, patient documents etc.) to meet local country requirements.
- →Compile IP release/Essential documents packages to ensure timely sites activation.
- →Support contract negotiations (CTAs) with sites/institutions.
- →Manage translation request and translations review of required for submissions local-language trial documentation.
- →Keep study management databases updated and file trial correspondence into the TMF as per SOPs and study plans.
- →Maintain ongoing status updates with study teams, sites, study PM team.
Requirements
~1 min read- Bachelor’s degree in Life Sciences, Nursing, or related field.
- Fluent English language.
- Minimum 2-3 years of recent actual experience with Start up activities in Estonia managing submission under CTR via CTIS.
- Strong knowledge in clinical research regulatory requirements at country and global levels as per GCP.
- Experienced user of Microsoft Office Suite.
- Attention to detail and time-management skills.
- Teamwork and collaboration within study teams as well as Clients/vendors as applicable.
Location & Eligibility
Where is the job
Estonia
Remote within one country
About this job
- Posted
- Today
Listing Details
- Posted
- November 4, 2026
- First seen
- November 4, 2026
- Last seen
- November 4, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 68%
- Scored at
- November 4, 2026
Signal breakdown
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Biomapas is a functional and full outsourcing solution provider to the global life science industry, with key expertise in Clinical Trials, Regulatory Affairs, Pharmacovigilance, and Medical Information.
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