RSU Specialist I, FSP Sponsor Dedicated

IQVIA LLC; México; A distancia; MXN 420.000 - 720.000; Jornada completa

Descripción de la vacante

IQVIA LLC in Mexico is seeking a Regulatory & Start Up Specialist 1, cFSP for Global Support Mexico. This full-time remote role drives site activation and regulatory deliverables, coordinating with sponsors, SAMs, and project teams to ensure SOP and timeline adherence.

The ideal candidate has a life sciences degree, 1+ year of clinical research start-up experience, and fluent English. Strong analytical, communication, and multitasking abilities are essential for fast-paced environments.

Formación

• Bachelor degree in life sciences or related field.
• 1+ years of clinical research experience and study start up management.
• Fluent English: written and oral communication.
• Strong analytical and critical thinking skills to evaluate issues.
• Good interpersonal skills and adaptability to changing requirements.

Responsabilidades

• Serve as SPOC in assigned studies for sites and project teams.
• Perform start up and site activation activities per regulations and SOPs.
• Prepare site regulatory documents for completeness and accuracy.
• Maintain internal systems and tracking tools with project data.
• Provide feedback on site performance metrics to management.
• Plan project timelines and establish monitoring measures.
• Inform team of completion of regulatory and contractual documents.
• Track progress and approval of regulatory, ethics, and IP release documents.
• Provide local expertise to SAMs during project planning.

Conocimientos

Regulatory knowledge

Clinical research experience

English fluency

Analytical thinking

Communication

Educación

Bachelor Degree in life sciences

Descripción del empleo

Regulatory & Start Up Specialist 1, cFSP - Global Support Mexico - Full Home Based role

Purpose: The RSU Specialist 1 proactively drives and executes start up and maintenance related activities and deliverables for assigned studies and sites in their assigned country.

Essential Functions

• Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary. Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines.
• Perform start up and site activation activities according to applicable regulations, SOPs and work instructions. Distribute completed documents to sites and internal project team members.
• Prepare site regulatory documents, reviewing for completeness and accuracy.
• Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.
• Review and provide feedback to management on site performance metrics.
• Review, establish and agree on project planning and project timelines. Ensure monitoring measures are in place and implement contingency plan as needed.
• Inform team members of completion of regulatory and contractual documents for individual sites.
• Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines.
• Provide local expertise to SAMs and project team during initial and on-going project timeline planning.
• Perform quality control of documents provided by sites.
• May have direct contact with sponsors on specific initiatives.

Qualifications

• Bachelor Degree in life sciences.
• +1 years of clinical research experience and study start up management experience.
• Fluent English: written and oral communication skills
• Good analytical and critical thinking skills and the ability to evaluate complex issues from multiple perspectives
• Good interpersonal skills with the ability to build trust and communicate with clarity, flexibility and adaptability to changing requirements
• Demonstration of successful execution, preferably in start up, and aptitude for managing multiple priorities in a fast-paced environment

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.