Remote Start-Up Specialist, Clinical Trials

Precision for Medicine; United States; Remote; USD 90,000 - 130,000; Full time

Benefits offered by this job

Remote work

Job summary

Precision for Medicine seeks a Start Up Specialist to join our growing team. Open to candidates with Site Start Up experience from a CRO, located in Hungary, Poland, Serbia, Slovakia or Romania, and fluent in Hungarian.

Key duties include regulatory submissions, site activation coordination, document translation, and cross-functional collaboration to ensure on-time study startup and regulatory compliance. You will maintain trackers and liaise with CA/EC to support timelines.

Qualifications

• Bachelor’s degree in life sciences or RN/Pharmacist qualification.
• Experience as Regulatory or Start Up specialist in CRO or pharma.
• Fluent in Hungarian and English; ability to support Hungarian sites.

Responsibilities

• Prepare regulatory submissions for CA/EC and local authorities with timelines.
• Maintain project plans, trackers and TMF readiness for studies.
• Coordinate translations and country/site start-up documentation.
• Collaborate with site CRA and cross-functional teams to activate sites.
• Monitor regulatory timelines and support budget negotiations when needed.

Skills

Regulatory Start-Up experience

Strong communication

Organizational skills

Hungarian fluency

English fluency

Education

Bachelor's degree in life sciences

RN or Pharmacist qualification

Advanced degree in medical or life sciences / RAC

Job description

Precision for Medicine seeks a Start Up Specialist to join our growing team. Open to candidates with Site Start Up experience from a CRO, located in Hungary, Poland, Serbia, Slovakia or Romania, and fluent in Hungarian.

Key duties include regulatory submissions, site activation coordination, document translation, and cross-functional collaboration to ensure on-time study startup and regulatory compliance. You will maintain trackers and liaise with CA/EC to support timelines.