Senior Clinical Trial Manager (LATAM)

We’re hiring a Senior Clinical Trial Manager to help build and lead our expanding clinical operations across Latin America . This is an exciting, high ‑ impact opportunity, supporting rapid growth across Mexico, Brazil, Argentina, Colombia, Chile, and Peru .

As the clinical lead, you’ll own the planning, execution, and oversight of clinical studies, serving as the primary client contact and ensuring delivery in compliance with protocol, SOPs, ICH ‑ GCP, and regulatory requirements. You’ll shape country ‑ level recruitment strategies, lead feasibility and site start ‑ up, guide monitoring and quality strategies, and mentor CRAs and partners as we scale a new regional team.

This role offers significant career growth , including opportunities to build teams, define processes, influence culture, and step into broader leadership and project management responsibilities as the region grows.

Essential functions of the job include but are not limited to:

Primary clinical point of contact with the client

Collaborate with PM on monthly invoicing and variance management of clinical budget

Develop study related clinical documents (e.g. clinical plans, Informed Consent Form templates, study specific forms and manuals, CRF completion guidelines, study trackers, PSV/SIV slides and other training materials)

Identify and develop training needs for CRAs and third-party vendors specific to the study, protocol and practices including presenting these at Investigator Meetings and Study Kick-off meetings

Generate potential site list from key stakeholders and drive site feasibility process

Identify potential risks to the enrollment targets based on feasibility analysis and site’s contracted commitment

Develop and finalize the country recruitment/retention strategy

Develop timely and effective communication and good working relationships with investigators and study team to ensure effective and timely feasibility, site start up, enrollment, maintenance and close out procedures

Lead internal clinical team meetings and sets expectations for clinical team of CRAs and CTAs

Address all CRA and site questions and maintains Frequently Asked Question (FAQ) log as appropriate

Support in planning and conducting investigator meetings

Review and/or approve of IP release packages

Oversee, support and track all submissions and approvals to Competent Authorities and IRB/Ethics Committees in conjunction with regulatory departments as applicable

Develop clinical monitoring strategies for assuring study timelines are met and assuring quality deliverables

Generate and utilizes metric reporting (e.g., CTMS, DM Query Trends, Outstanding Monitoring Reports) to ensure that the study is conducted per plan and communicates issues to PM and CRAs as appropriate

Responsible for eTMF implementation and management

Collaborate with PM, CRAs and QA to develop any Corrective and Preventative Action Plan (CAPA) and is accountable for implementation and timely closure

Accountable to assist sites, internal staff and CRAs with the preparation for GCP audits

Work closely with PM for project-specific resourcing issues

Escalate pertinent CRA performance and site compliance issues when necessary