Lead day-to-day operational execution and oversight of trials.
Develop and maintain study timelines, milestones, plans.
Coordinate CROs, vendors, sites, and partners.
Monitor progress, identify risks, mitigate delays.
Ensure activities comply with ICH-GCP, regs, SOPs.
Collaborate with cross-functional teams (Ops, Regulatory, Medical, Data, Pharmacovigilance

🎯 Requirements

Bachelor's in Life Sciences, Pharmacy, Nursing, Medicine, or related field.
At least 3 years in clinical research, incl. CTM/Operations.
Experience managing trials in pharma/CRO/related orgs.
Strong knowledge of ICH-GCP and regulatory requirements.
Experience coordinating CROs, vendors, sites, cross-functional teams.
Strong PM, organizational, analytical, problem-solving skills.

🎁 Benefits

Competitive salary paid in USD.
100% remote work from Latin America.
Long-term professional engagement.
Independent Contractor arrangement.
10 business days / 2 weeks PTO.
Paid US-calendar holidays.

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