Remote Clinical Job at Premier Research | Apply Now
A rare chance has emerged for aspiring professionals to secure a remote clinical job as a Clinical Trial Associate at Premier Research in Hungary. This position offers a unique opportunity to contribute to life sciences while working in a flexible environment.
Job Details
- Job Title: Clinical Trial Associate
- Job Location: Remote, Hungary
- Job Requisition ID: R6522
About Premier Research
Premier Research is a global contract research organization that specializes in helping biotech, medtech, and specialty pharma companies transform innovative ideas into life-saving medicines, devices, and diagnostics. With a strong commitment to advancing healthcare, Premier Research operates in various countries, including Hungary, and values its team members as the most important asset in delivering successful outcomes. This organization is dedicated to fostering a collaborative environment that encourages growth and development, making it an ideal place for a life sciences job.
Remote Clinical Job Description
As a Clinical Trial Associate, the selected candidate will play a vital role in supporting the Clinical Monitoring, Site Management, and SSU teams. The responsibilities include maintaining the Trial Master File (TMF) and electronic Trial Master File (eTMF) in collaboration with the clinical team, ensuring compliance with all regulatory requirements, and supporting the overall success of clinical trials.
Eligibility Criteria
- Undergraduate degree or equivalent in life sciences, or medical documentation from an accredited institution.
- Prior experience in a similar role is preferred.
- A minimum of 1 year of experience as a Clinical Trial Associate or in a related position.
- Fluent verbal and written English skills.
- Knowledge of ICH/GCP, essential documents, and ALCOA+ principles.
Remote Clinical Job – Key Responsibilities
This remote clinical job will involve the following key tasks:
- Maintaining the TMF/eTMF in accordance with the organization’s or Sponsor’s SOPs and regulatory requirements.
- Creating and maintaining placeholders in the TMF based on filing plans, expired documents, and study milestones.
- Reviewing site documents to ensure they meet all standards set by the company, sponsor, and regulatory authorities.
- Performing completeness checks of relevant eTMF sections throughout the trial process.
- Conducting follow-ups on TMF queries to ensure timely resolution.
- Running and distributing eTMF reports to facilitate quality and compliance.
- Assisting with essential document collection during startup, maintenance, and close-out phases.
- Supporting the translation of site documents when required.
In summary, this remote clinical job as a Clinical Trial Associate at Premier Research presents an excellent opportunity for qualified candidates to engage in meaningful work within the life sciences sector. With a focus on innovation and collaboration, Premier Research is poised to make a significant impact in the healthcare industry. Interested candidates are encouraged to apply before the deadline to seize this opportunity.
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