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Open nowPosted 18 hours ago

Clinical Operations Lead

PSI CRO195 open roles

Where
Buenos Aires, Argentina
Work mode
Hybrid
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Your applicationOpen nowClinical Operations LeadPSI CRO · Buenos Aires, Argentina

  1. YouYes, apply to this one.

  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on PSI CRO's own form.

The reply lands in your private mailbox

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The clock on this job

Early applications get read.

13.5% of postings close within 7 days. Measured by our own scanner across the market. PSI CRO postings stay open a median of 19 days.

Share of postings closed within
  1. 2.3%1 day
  2. 4.6%3 days
  3. 13.5%7 days
  4. 21.8%14 days
  5. 36.6%30 days
  6. 58.9%60 days
This job: posted 18 hours ago

PSI CRO median: 19 days open

The posting

Company Description

PSI is a leading Contract Research Organization with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.

Job Description

We’re looking for a knowledgeable, proactive, and result-oriented professional to join our management team and help lead and further develop our Clinical Operations team in Latin America region. You will lead and mentor a high-performing team while ensuring efficient resource utilization, operational excellence, and the successful delivery of clinical trials. In this role, you will enjoy a broad range of operational and strategic management responsibilities, while contributing to the continued growth and success of the region.

The scope of responsibilities will include:

  • Line manage, coach, mentor, and develop Clinical Operations staff across multiple experience levels.
  • Supervises and conducts training of Monitors.
  • Mentors Monitors.
  • Plans and conducts supervised monitoring visits with training, authorization, and ongoing assessment purposes.
  • Supports professional development of Monitors.
  • Contributes to the performance appraisal of Monitors.
  • Supports Clinical Operations Managers with resource allocation and utilization of departmental staff.
  • Performs other Clinical Operations supervisory tasks.

Qualifications

  • MD, PharmD, or a university degree in Life Sciences
  • Previous clinical research industry experience is required.
  • Previous experience working independently as an onsite Clinical Research Associate (CRA) is required (minimum of 4 years)
  • Previous experience managing or mentoring clinical research professionals in a CRO, sponsor, or related clinical research environment.
  • Previous experience with Oncology or IBD is a plus.
  • Strong leadership, coaching, and employee development skills.
  • Experience with resource planning, workload management, and performance management.
  • Working knowledge of ICH-GCP, applicable regulatory requirements, and clinical trial operations.
  • Experience supporting audits, inspections, and quality initiatives is preferred.
  • Excellent communication, organizational, and problem-solving skills.
  • Proficiency with Microsoft Office applications and clinical research systems.
  • Advanced English proficiency (written and spoken).
  • Strong interpersonal skills with the ability to build trust, foster collaboration, and develop high-performing teams.

Additional Information

Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.

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  2. 25 readers review it

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    The review screen in CV Rocket: how each CV was read, round by round.

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    An interview invitation in the CV Rocket inbox, added to the candidate's calendar.
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