Empleos de ICON Clinical Research en México

About the Role · As a Site Contracts Negotiator II at ICON, you will be working from home to negotiate and maintain clinical trial agreements with study sites. · You will be responsible for drafting, reviewing, and finalizing agreements while ensuring they align with departmental ...

TMF Specialist I · A leading clinical research organization is seeking a Trial Master File Specialist I. · Responsibilities include managing TMF documentation, ensuring compliance with client requirements and internal procedures. · Ideal candidates should have a Bachelor's degree ...

Senior Site Contracts Negotiator · In this role, you will be responsible for negotiating and maintaining clinical trial agreements with investigative sites. · Responsibilities: · Drafts, reviews, negotiates, and finalizes clinical trial agreements using critical thinking and adhe ...

Role: Trial Master File Specialist I · This role involves becoming familiar with Trial Master File (TMF) documentation and document management activities. · Gain familiarity with Trial Master File (TMF) documentation and document management processes. · Contribute to client servi ...

Senior Manager, Clinical Supplies · Oversight of clinical supplies planning, procurement, and distribution. · About the Role: · Lead a diverse team with extensive experience in clinical supplies management. · Ensure compliance with regulatory standards. · ...

Key Responsibilities: · ICF Development and Review: Prepare, review, and approve Subject Information Sheets (SIS) and Informed Consent Forms (ICF) for global master templates, country-specific versions, and site-specific adaptations. · Compliance Ensurance: Apply proficient knowl ...

A leading healthcare research organization is seeking a skilled professional to manage clinical trial agreements in a remote capacity. · Key Responsibilities: · Drafting and finalizing agreements · Ensuring compliance with regulations · Maintaining effective stakeholder communica ...

Overview · Clinical supply chain logistics is a critical component of the clinical research process. ICON plc is a world-leading healthcare intelligence and clinical research organization that fosters an inclusive environment driving innovation and excellence. · The Manager, Glob ...

About the Role · The Trial Master File Specialist I will manage TMF documentation, ensuring compliance with client requirements and internal procedures. · Key Responsibilities · Manage TMF documentation · Ensure compliance with client requirements and internal procedures · Requir ...

Job Summary: · This is an office-based hybrid role in Mexico City only, working 03 days in office and 02 days from home. The ideal candidate will have a Bachelor's degree in a relevant field, full proficiency in English, prior experience in clinical research and/or document manag ...

Job Description: · As a Senior ICF Strategist at icon-clinical-research, you will play a crucial role in developing and reviewing Informed Consent Forms (ICFs) and Subject Information Sheets (SIS). · Key Responsibilities: · Ensure compliance with guidelines for ICF development. · ...

A leading healthcare intelligence firm in Mexico City is seeking a Global Supply Chain Manager. This role involves overseeing supply chain processes for clinical research projects, developing strategies and leading a team. · The ideal candidate will have significant experience in ...

Clinical Trial Material Summary: Senior Manager, Clinical Supplies Management · Job Description: · We are seeking a Senior Manager, Clinical Supplies Management to oversee the planning, procurement, and distribution of clinical supplies for smooth clinical trial execution. As a l ...

Clinical Supplies Project Manager · As a Clinical Supplies Project Manager at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. · Oversee th ...

Clinical Supply Chain Associate Manager is responsible for overseeing the management and distribution of clinical trial materials, ensuring timely delivery and compliance with regulatory standards. They will contribute to the success of clinical research by optimizing supply chai ...

Job Summary · A leading clinical research organization in Mexico City is seeking a Senior Regulatory Technician to work with the Clinical Trials Information System, manage regulatory submissions, and ensure compliance. · About this Role · Work with the Clinical Trials Information ...

Regulatory Technician Role Overview · The Regulatory Technician plays a crucial role in ensuring compliance and quality in clinical trials. The individual will be responsible for managing data and documents through the Clinical Trials Information System (CTIS), collaborating with ...

Clinical Supplies Project Manager · A leading clinical research organization is seeking a Clinical Supplies Project Manager in Mexico City. The ideal candidate will oversee clinical supplies projects, ensuring timely delivery and compliance with regulatory requirements. · Key Res ...

Senior Regulatory Technician · We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. As a Senior Regulatory Technician, you will work with the Clinical Trials Inf ...

About the Role · As a Senior Site Contracts Negotiator, you will play a critical role in managing clinical trial agreements from a home-based position in Mexico. · Key Responsibilities · Drafting agreements and maintaining stakeholder communications · Collaborating with cross-fun ...