Lead CRA.

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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 and timelines complying with AZ P ...

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Clinical Trial Manager

ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations. · With ou ...

Lead CRA.

Job Description

In the role of Sr CRA II (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 Sr CRA II (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 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.

Job DescriptionIn the role of Sr CRA II (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...

Performs and coordinates all aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. Manages procedures and guidelines from different sponsors and/or monitoring environments ( FSO, FSP, Government, etc.). Acts as a site processes...

Job DescriptionIn the role of Sr CRA II (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...

Job Description In the role of Sr CRA II (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: ...

Job Description In the role of Sr CRA II (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: ...

Job DescriptionIn the role of Sr CRA II (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...

Job Overview Leads and oversees the execution of clinical projects and research studies in accordance with global and local regulations to best meet customer needs while working toward organizational goals and strategies. Manages the operational elements of clinical projects to deliver contracted clinical services to the customer’s satisfaction....

Description Job Overview Leads and oversees the execution of clinical projects and research studies in accordance with global and local regulations to best meet customer needs while working toward organizational goals and strategies. Manages the operational elements of clinical projects to deliver contracted clinical services to the customer’s...

Work Model: Hybrid Locality: Ciudad de Mexico Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you About the Role: The SSO Clinical Project Manager (CPM) is accountable for the day-to-day planning, executing and reporting, (from first site initiation visit to and including study site...

Specialist, Country Study Start Up Primary Mexico City, Mexico Req ID R00101174 Category Clinical Research Division AbbVie Purpose: The Specialist, Country SSU proactively drives and executes all start up and maintenance related activities and deliverables for assigned studies and sites in their assigned country or countries. Primary...

Job Overview Manage the execution of the assigned clinical study (ies) from initiation through to closeout. Ensure that clinical study management and project deliverables are on time and is in accordance with standard operating procedures (SOPs), policies and practices. To provide project related support and assistance across multiple projects, sites and...

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Senior Site Selection Lead page is loaded · Senior Site Selection Lead · Apply locations Mexico City Mexico Remote_Mexico time type Full time posted on Posted 30+ Days Ago job requisition id The Sr. Site Selection Lead will play an integral role in collaborating closely with Gl ...

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Parexel FSP is hiring multiple Site Care Partners to support the Argentina, Chile and Brazil region--these are great opportunities for experienced CRAs seeking career advancement · Job Summary · The Site Care Partner is the main client point of contact for investigative sites thr ...

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Workforce Analytics Specialist #J-18808-Ljbffr

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