or apply directly on Precision for Medicine's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 13 days Precision for Medicine's roles stay open a median of 41 days
- Reposted
- No
- Salary listed
- No 0% of Precision for Medicine's roles list one
- Ghost-job risk at Precision for Medicine
- high 58 stale, 4 reposted of 122 open
- Hiring momentum
- 246 roles opened in the last 90 days ↑ up vs. the prior 90 days
- Last confirmed on the employer's board
- 2026-09-17
Measured from postings appearing on and disappearing from Precision for Medicine's own greenhouse board since 2026-08-03. Full hiring picture for Precision for Medicine.
About this role
The Regulatory and Start Up Specialist at Precision for Medicine will be responsible for ensuring site activation readiness in Spain, focusing on regulatory submissions, contracts, and budgeting negotiations. Daily tasks include preparing clinical trial application forms, interacting with competent authorities and ethics committees, maintaining project plans, and collaborating with various teams to ensure compliance with local regulations and timely approvals for clinical trials.
- benefits
- 1/5
- freshness
- 4/5
- career value
- 4/5
- role clarity
- 4/5
- pay transparency
- 0/5
Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Precision for Medicine as an employer.
What you need
- Bachelor’s degree in life sciences or related field, or Registered Nurse (RN) or equivalent
- Demonstrated experience in contracts and budgeting negotiation
- Previous experience as a Regulatory or Start Up specialist in a CRO or pharmaceutical/biotech industry
- Strong communication and organizational skills
- Experience using computerized information systems, electronic spreadsheets, word processing and electronic mail
- Fluency in English and Spanish
Nice to have
- Qualification in Pharmacy or work experience as a Pharmacist
- Relevant regulatory and site start-up 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
Worth weighing
- Remote position based in Spain
- No specific salary or benefits mentioned in the posting
- Role involves significant interaction with regulatory bodies and requires strong negotiation skills
- Experience with local clinical trial laws and regulations is crucial for success
Summarised from Precision for Medicine's posting. Read the full original.
Listed by Precision for Medicine on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.
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