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Precision Medicine Group

Senior Regulatory and Start Up Specialist (Argentina)

Precision Medicine Group · Remote, Argentina

Posted 9 days ago

or apply directly on Precision Medicine Group's site. We never take the application ourselves.

Is this posting real?

This role has been open
9 days
Precision Medicine Group's roles stay open a median of 45 days
Reposted
No
Salary listed
No
0% of Precision Medicine Group's roles list one
Ghost-job risk at Precision Medicine Group
high
85 stale, 8 reposted of 157 open
Hiring momentum
309 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 Medicine Group's own greenhouse board since 2026-08-03. Full hiring picture for Precision Medicine Group.

About this role

The Senior Regulatory and Start Up Specialist will be responsible for managing regulatory submissions and site start-up activities for clinical trials in Argentina. This includes preparing Clinical Trial Application Forms, interacting with Competent Authorities and Ethics Committees, and ensuring compliance with local and international regulations. The role also involves mentoring junior staff, maintaining project plans, and collaborating with various teams to ensure timely site activation.

Our read on this posting2.8out of 5
benefits
1/5
freshness
4/5
career value
4/5
role clarity
5/5
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 Medicine Group as an employer.

What you need

  • Bachelors’ degree in life sciences or related field, or Registered Nurse (RN)
  • 3.5 years or more as a Regulatory or Start Up specialist in a CRO or pharmaceutical/biotech industry
  • Ability to communicate both verbally and in writing in English proficiently
  • Excellent communication and organizational skills
  • Experience using computerized information systems, electronic spreadsheets, word processing and electronic mail
  • Ability to prioritize workload to meet deadlines

Nice to have

  • Relevant regulatory and site start-up experience for the particular country
  • Experience using milestone tracking tools/systems
  • Advanced degree in medical or life sciences (MD, PhD, PharmD)/RAC certification/Masters in Regulatory Science
  • Can assist junior SU specialists in problem resolution

Worth weighing

  • Role involves significant regulatory responsibilities which may require ongoing education and adaptation to local laws
  • No specific salary or benefits mentioned in the posting
  • Remote position may require flexibility in working hours to collaborate with teams across different countries

Summarised from Precision Medicine Group's posting. Read the full original.

Listed by Precision Medicine Group on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.

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