Empleos de ICON Clinical Research en México

A leading clinical research organization seeks a Clinical Data Engineer to develop data science solutions for clinical trials. · Key Responsibilities · Manage programming activities · Evaluate and ensure data integrity · Skills Required: · Data Science degree or equivalent experi ...

Overview · Clinical trials are at the forefront of shaping the future of healthcare. · This Clinical Trial Associate role will be key in driving innovation and excellence within our team at ICON plc, a world-leading healthcare intelligence and clinical research organization. · ...

Job Description · A global healthcare organization seeks a Clinical Supplies Manager in Mexico City to oversee clinical trials planning and execution. · The role involves collaborating with cross-functional teams, ensuring compliance with regulations, and managing timelines and b ...

Proposals Development Specialist II · This role involves leading the development of client proposals and collaborating with various teams to ensure proposal accuracy. · Bachelor's degree required · 2-3 years of relevant experience preferred · ...

Clinical Supplies Associate Manager Job Description · Job Summary: · Oversight of planning procurement distribution for clinical trials ensuring timely delivery compliance with regulatory standards. · Main Responsibilities: · Leading supply chain optimization processes inventory ...

Clinical Site Management Associate II · About this role: · In this challenging and rewarding role at our leading clinical research organization in Mexico City you will be responsible for ensuring compliance with clinical trial protocols. · Coordinating site monitoring visits to e ...

Job Description: · The Site Management Associate I will support clinical trial site management by ensuring compliance with protocols and providing administrative assistance. · Site monitoring · Administrative support · ...

Clinical Operations Management · ICON plc is a world-leading healthcare intelligence and clinical research organization. · The company fosters an inclusive environment driving innovation and excellence. · Key Responsibilities · Lead operational planning and execution of clinical ...

Job Overview · A Project Associate role at ICON plc involves organizing project teams and clients meetings scheduling preparing meeting materials binder agendas minutes managing study information supplies generating essential documents organizational charts team calendars newslet ...

At our clinical research organization in Mexico City, we're seeking a Central Review Coordinator to facilitate centralized review activities in clinical trials. · About the Role · Coordinate logistics for clinical trial reviews · Collaborate with cross-functional teams to ensure ...

Clinical trials rely on efficient supply chain management to ensure timely and compliant distribution of clinical supplies. · Key Responsibilities: · Manage planning coordination execution of clinical trial supplies ensuring timely compliant distribution · Collaborate with clinic ...

ICON plc seeks a Proposals Development Associate II in Mexico City (Office based) to contribute to client proposal development and success. · Main Responsibilities · Lead proposal preparation with cost estimates, timelines, and scope of work documents. · Collaborate with clinical ...

Job Description · A global clinical research organization is seeking a highly skilled Manager, Business Continuity · To develop and implement strategies that ensure operational resilience during business interruptions. · The ideal candidate will have a strong background in busine ...

Strategic Clinical Data Science Lead · We are seeking a Senior Clinical Data Science Lead to oversee data review activities in Mexico. · Manage timelines · Perform analytic reviews · The ideal candidate will have 5+ years of experience in clinical data management and proficiency ...

Mexico City-based ICON plc seeks a Site Management Associate I to support clinical trial site management. · Key Responsibilities · Assist with monitoring clinical trial sites, ensuring adherence to study protocols and GCP guidelines. · Support site management activities, includin ...

Job Description: · A leading clinical research organization is seeking an Investigator Payments Associate in Mexico City. · Analyze and evaluate payments ensuring compliance and accuracy · Review contracts maintaining communication with investigators collaborating project teams t ...

Job Description · The Site Management Associate II will play a vital role in supporting clinical trial sites by ensuring compliance with study protocols and regulatory requirements. · Coordinate monitoring activities at clinical trial sites, ensuring adherence to study protocols. ...

About this role: · This is a hybrid position supporting site partners in collecting and reviewing essential start-up submission packages while ensuring compliance with regulatory guidelines. · Support site partners in collecting and reviewing essential start-up submission package ...

Clinical Supplies Manager Role · Oversee clinical supplies projects, ensuring timely delivery and regulatory compliance. · Collaborate with cross-functional teams to design effective strategies for clinical trial supply management. · We are seeking a Clinical Supplies Manager to ...

Senior Clinical Supply Chain Specialist · This is a senior-level position within our clinical research organization that requires expertise in managing supply chains for clinical trials. We are seeking an individual with advanced education in relevant fields like logistics or bus ...