Skills this job asks for
LeadershipGoogle CloudEnglish
Add your CV (free) to see which of these your CV is missing.
Sponsorship verdict
No sponsorship evidence yet
No government record and no wording either way. Not a refusal: ask the recruiter.
-
?
No government sponsor record hereNo government sponsor record covers this employer in this country.
-
?
The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
-
?
Can’t check pay against the visa rulesWe don’t have visa salary rules for this country yet.
-
✓
Confirmed live todayWhen a source last listed this job as open.
Details and sources
A verdict summarises public evidence. It is not legal advice and never a guarantee: the employer and the immigration authority decide. Sign in to factor in where you can already work.
Before you apply
Sponsorship unknown
No register record and no sponsorship wording in the posting. Worth asking the employer before investing significant time.
These come from the posting’s own wording. Read the original listing to confirm. See better-fit alternatives →
About the role
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.
• 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.
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.
Apply on employer site ↗