Regulatory and Start Up Specialist - Fluent in Hungarian

Precision for Medicine; Polska; Hybrid; PLN 120,000 - 180,000; Full time

Job summary

Precision for Medicine is seeking a Regulatory and Start Up Specialist fluent in Hungarian to join our growing team. This remote Poland position involves preparing submissions, coordinating with authorities, and maintaining regulatory plans to enable timely site activation.

The ideal candidate has a life sciences degree, Hungarian fluency, English fluency, and prior regulatory/start-up experience in CRO or pharma. Strong communication and organization are essential in a global setting.

Qualifications

• Bachelor’s degree in life sciences or related field.
• Fluency in English and Hungarian.
• Experience as Regulatory or Start Up specialist in CRO or pharma.
• Knowledge of local regulatory processes and ICH-GCP.

Responsibilities

• Prepare Clinical Trial Application forms and submission dossiers to authorities and ethics committees.
• Coordinate CA/EC submissions and respond to inquiries from authorities.
• Provide updates on submissions to Start Up/Regulatory leads and project teams.
• Maintain regulatory trackers, plans, and intelligence tools.
• Support start-up plans, IMP release requirements, and essential document review.
• Collaborate with site CRAs to ensure alignment and site activation readiness.
• Collect and manage essential documents for site activation and IMP release.
• Customize patient information sheets and consent forms per country/site.
• Coordinate translations of documents and liaise with cross-functional teams.
• Monitor timelines for CA/EC/IRB submissions and site activation milestones.
• Assist in budget negotiation and investigator contract execution as needed.
• Keep updated on local clinical trial laws and maintain TMF readiness.

Skills

Hungarian fluency

Strong communication

Organizational skills

Regulatory/start-up experience

Education

Bachelor's in life sciences

RN or Pharmacy qualification (beneficial)

Job description

Regulatory and Start Up Specialist - Fluent in Hungarian

Remote, Poland

Precision for Medicine is a Clinical Research Organization. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology, in addition to working across other therapeutic areas.

As our company continues we grow we are seeking a Regulatory and Start Up Specialist to join our growing team.

Essential functions of the job include but are not limited to:

• Preparation of Clinical Trial Application Forms as well as preparation of submission dossier (initial and amendments/notifications) for submission to Competent Authorities, Ethics Committees, and other applicable local bodies according to local requirements and within required timelines to obtain all necessary authorizations/approvals for the conduct of the Clinical Trial according to international and local/national applicable regulations, company SOPs and principles of ICH-GCP.
• Interaction with CA/EC for study purposes and handling responses to the CA/EC.
• Providing regular updates about CA and EC submissions to the Start Up Lead and/or Regulatory Lead assigned to the study and to Project Manager/Project Team
• Maintenance of project plans, project trackers and regulatory intelligence tools as it pertains to assigned responsibilities and to keep Regulatory Leadership
• Preparation/Support the development of study specific start-up plans, IMP release requirements and essential document review criteria.
• Partner with the assigned site CRA to ensure alignment in communication and secure site
• review and manage collection of essential documents required for site activation/IMP release.
• Customize country/site specific Patient Information Sheet and Informed Consent Form.
• Responsible for/facilitates the translation and co-ordination of translations for documents.
• Maintain communication with other key functions participating to country start up e., Feasibility, Clinical Operations, Project Management, Regulatory, and Site Contracts management group on project specific status and deliverables.
• Act as SME for collection and maintenance of site level critical path to Site Activation data points, including but not limited to Competent Authority, local IRB/Ethics Committee (EC) timelines, site contracts and budget negotiation requirements for and other required reviews to secure on time site activation for the assigned sites in the country.
• When required, participate/support the negotiation of study budgets and the execution of investigator contracts under directions of Site Contract Management department/designee department.
• May participate/support feasibility group in site outreach to assess potential interest of investigators to a potential study.
• Keep an updated knowledge of the local clinical trial laws, regulations and help distributing their knowledge within PFM to ensure the conduct of Clinical Trials according to international and local/national applicable regulations.
• Maintain audit/inspection readiness at all times and file documents as per TMF plan and/ or study specific plans in the relevant TMF
• May support the clinical team performing Pre-Study Site Visits.

The ideal candidate will have:

• Bachelor’s degree in life sciences or related field (ideally in a scientific or healthcare discipline), or Registered Nurse (RN) or equivalent combination of education, training, and experience.
• A qualification in Pharmacy/ work experience as a Pharmacist would be highly beneficial.
• Demonstrated experience as a Regulatory or Start Up specialist (or comparable role) in either a CRO or pharmaceutical/ biotech industry or equivalent, relevant experience and/or demonstrated competencies.
• Fluency in Hungarian language as this position will support Hungarian sites.

Other Required:

• Strong communication and organizational skills.
• Experience using computerized information systems, electronic spreadsheets, word processing and electronic mail required.
• Fluency in English.

Preferred:

• Relevant regulatory and site start-up (feasibility, contract negotiations, CA/ EC/ IRB submissions) experience.
• Experience using milestone tracking tools/systems.
• Ability to prioritize workload to meet deadlines
• Advanced degree in medical or life sciences (MD, PhD, PharmD)/RAC certification/Masters in Regulatory Science.

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Candidate must be legally authorized to work in the country of employment without employer sponsorship.

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