Senior Clinical Research Associate (Chile)
Precision Medicine Group · Remote, Chile
Posted 13 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
- 13 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 Clinical Research Associate (CRA) will oversee site management for clinical studies in Chile, ensuring patient safety and data quality. Responsibilities include monitoring clinical trials, managing site start-up procedures, conducting site visits, and mentoring junior staff. The role also involves communication with site personnel and project managers, as well as documentation and compliance with regulatory standards.
- 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 Medicine Group as an employer.
What you need
- 4-year college degree or equivalent experience in a scientific or healthcare discipline
- 5 years or more as a CRA in either a CRO or pharmaceutical/biotech industry or equivalent, relevant experience and/or demonstrated competencies
- Significant site management experience or equivalent experience in clinical research
- Ability to communicate both verbally and in writing in English proficiently (Professional level)
Nice to have
- Graduate, postgraduate degree
- Experience monitoring in rare and complex therapeutic areas
- Experience monitoring EDC trials and EHR records
- Experience in biopharma or relevant therapeutic area
- Relevant site start-up experience for the country
Worth weighing
- No salary listed
- Remote position with travel requirements up to 60%
- Focus on training and mentoring junior staff may increase workload
- Role involves significant documentation and compliance responsibilities
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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