Lead CRA

hace 7 días


Ciudad de México, Ciudad de México PSC Industries A tiempo completo

i Ad · Clinical Project Manager · Clinical Project Manager · Location : CDMX · Hybrid Work ( 3 office days a week) · Role description · To lead Local Study Team(s) (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budg ...

i Ad

Lead Cra

i Ad Clinical Project Manager · Clinical Project Manager · Location : CDMX · Hybrid Work ( 3 office days a week) · Role description · To lead Local Study Team(s) (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budget ...

i Ad

Regional Clinical Research Associate Level II

Regional Clinical Research Associate Level II & III Mexico Business Title · Regional Clinical Research Associate Level II & III · Requisition ID · EM-R-CRA-1003 · Job Category · Regional Clinical Research · Locations Job Description Job Summary: · Assures the implementation ...

Lead CRA.

Job Description

In the role of Lead Monitor, you will manage local Monitors, supervising clinical monitoring and site management activities to verify the protection of trial subjects' rights, safety and well-being, data quality and study compliance on a country/regional level.

Only CVs in English will be considered.

You will:

Facilitate regional projects as Lead Monitor and supervise study activities, timelines and schedules Train Monitors in annotated monitoring visit reports Review monitoring reports and support monitors in their activities Act as the main communication line between Monitor and Regional Lead Facilitatesite budgets and contract negotiations Be a point of contact for in-house support services and vendors Communicate with internal project teams regarding study progress and lead project team calls on the country level Participate in quality control and compliance monitoring May need to monitor and manage sites (if applicable) May need to supervise monitors on site Oversee and maintain study-specific and corporate tracking systems at site and country level

Mexico City PSI A tiempo completo

Job Description

In the role of Lead Monitor, you will manage local Monitors, supervising clinical monitoring and site management activities to verify the protection of trial subjects' rights, safety and well-being, data quality and study compliance on a country/regional level.

Only CVs in English will be considered.

You will:

Facilitate regional projects as Lead Monitor and supervise study activities, timelines and schedules Train Monitors in annotated monitoring visit reports Review monitoring reports and support monitors in their activities Act as the main communication line between Monitor and Regional Lead Facilitatesite budgets and contract negotiations Be a point of contact for in-house support services and vendors Communicate with internal project teams regarding study progress and lead project team calls on the country level Participate in quality control and compliance monitoring May need to monitor and manage sites (if applicable) May need to supervise monitors on site Oversee and maintain study-specific and corporate tracking systems at site and country level

Qualifications

College/University degree in Life Sciences, Pharmacy, RN or an equivalent combination of education, training & experience Participation in clinical projects as a Lead/Senior Monitor At least 4 years of experience as Senior CRA Independent on-sitemonitoring experience Full working proficiency in English and Spanish PC skills to be able to work with MS Word, Excel and PowerPoint Ability to plan, multitask and work in a dynamic team environment Communication, leadership, and problem-solving skills Ability to travel

Additional Information

Advance your career in clinical research, overseeing a variety of tasks and growing with the company. You will work closely with driven and dedicated cross-functional teams, get all support and ownership of your projects.

i Ad

Regional Clinical Research Associate Level II

Regional Clinical Research Associate Level II & III Mexico Business Title · Regional Clinical Research Associate Level II & III · Requisition ID · EM-R-CRA-1003 · Job Category · Regional Clinical Research · Locations Job Description Job Summary: · Assures the implementation ...

i Ad

Senior Clinical Research Associate II (Lead Monitor)

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do.A dynamic, global company founded in 1995, we bring together more than 2,500 driven, dedicated and passionate individuals.We work on the frontline of medical sci ...

i Ad

· Job Overview · Leader of the Centralized Monitoring team, partner with the project and clinical lead to achieve the delivery of the project's overall objectives to the sponsor's satisfaction per contract, while optimizing speed, quality and cost of delivery and in accordance w ...

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Project Manager

General Activities: Manages clinical investigational sites. Trains and provides direction to the investigators and the staff of the sites. Reviews, verifies and ensures that clinical documentation fulfils all protocol, GCP and regulatory requirements and maintains drug accountabi ...

i Ad

Associate Project Manager

Associate Project Manager · Location: Office Based Hybrid model - Mexico City - Insurgentes Sur. · ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pha ...

i Ad

Job Description Performs review of clinical monitoring visit reports for allocated projects ensuring consistency across protocols and/or regions and escalates any protocol, site, and/or CRA issues or trends noted during the report review process to CTM. · Job Description Essentia ...

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