Clinical Research Associate

hace 4 semanas


Xico, México Icon A tiempo completo

Study Start Up Associate I Role Overview

At ICON, we're seeking a highly skilled Study Start Up Associate I to join our dynamic team. As a key member of our regulatory submissions team, you will play a pivotal role in facilitating the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and therapies.

Key Responsibilities:

  • Assist in the preparation and submission of regulatory documents, such as clinical trial applications and ethics committee submissions.
  • Coordinate with internal and external stakeholders to obtain necessary approvals and authorizations for study initiation.
  • Maintain accurate and up-to-date records of regulatory submissions and approvals.
  • Support study teams in the development of study documents, including protocols, informed consent forms, and investigator brochures.
  • Participate in study start-up meetings and provide input on regulatory requirements and timelines.

Requirements:

  • Bachelor's degree in life sciences or a related field.
  • Previous experience in the pharmaceutical industry or clinical research, preferably in start-up, regulatory affairs, or a similar role.
  • Knowledge of local and/or international regulatory processes, including submissions to regulatory authorities and ethics committees.
  • Ability to read and understand clinical protocols, regulatory documents, and study-specific processes.
  • Strong attention to detail and organizational skills.
  • Ability to work independently and manage multiple tasks simultaneously in a fast-paced environment.
  • Excellent communication skills in English and Spanish.

Benefits of Working at ICON:

At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best-in-class employee benefits, supportive policies, and wellbeing initiatives are tailored to support you and your family at all stages of your career.

ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.



  • Xico, México Thermo Fisher Scientific A tiempo completo

    Clinical Research Associate RoleAt Thermo Fisher Scientific, we are seeking a skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for performing and coordinating all aspects of the clinical monitoring and site management process.Key Responsibilities:• Monitor investigator sites with a risk-based...


  • Xico, México Thermo Fisher Scientific A tiempo completo

    **Clinical Research Associate Role at Thermo Fisher Scientific**We are seeking a highly skilled Clinical Research Associate to join our team. As a key member of our clinical research services team, you will play a crucial role in bringing cures to market.**Key Responsibilities:**Manage metrics in various systemsCoordinate and support assigned PSS staff and...


  • Xico, México Icon Plc A tiempo completo

    At ICON Plc, we're seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for overseeing the day-to-day execution and site progress for all aspects and tasks related to site activation for assigned projects and sites.You will assist and engage with sites to ensure that site staff team...


  • Xico, México Thermo Fisher Scientific A tiempo completo

    **About the Role**At Thermo Fisher Scientific, we're committed to delivering life-changing therapies to patients worldwide. As a Clinical Research Associate, you'll play a vital role in our mission by providing remote support to our clients and ensuring the success of their clinical trials.**Key Responsibilities**Perform remote activities on assigned...


  • Xico, México Icon Plc A tiempo completo

    Job Title: Clinical Research AssociateAt ICON, we're driven by a shared vision to advance and improve patients' lives. Our diverse teams enable us to become a better partner to our customers and help us to deliver excellence in drug development.We're looking for a talented Clinical Research Associate to join our Study Start Up Team. As a key member of our...


  • Xico, México Thermo Fisher Scientific A tiempo completo

    Job SummaryThermo Fisher Scientific is seeking a skilled Clinical Research Associate to join our team. The ideal candidate will have a strong background in clinical research and a proven track record of ensuring regulatory compliance in a fast-paced environment.Key Responsibilities- Conduct on-site monitoring visits to ensure compliance with regulatory...


  • Xico, México Icon Plc A tiempo completo

    Job Title: Clinical Research AssociateAt ICON, we're driven by a shared vision to advance and improve patients' lives. Our diverse teams enable us to become a better partner to our customers and help us deliver excellence to our clients and patients at every touch-point.We're seeking a talented Clinical Research Associate to join our Study Start Up Team. As...


  • Xico, México Fortrea A tiempo completo

    Job Description:Job Title: Clinical Research Associate ICompany: FortreaLocation: MexicoJob Type: Full-timeExperience: 2 years (minimum)Job Description:Fortrea is seeking a highly skilled Clinical Research Associate I to join our team in Mexico. As a Clinical Research Associate I, you will be responsible for ensuring the integrity of clinical trials by...


  • Xico, México Psi Cro A tiempo completo

    At Psi Cro, we're a dynamic, global company founded in 1995, bringing together over 2,800 driven individuals. We work on the frontline of medical science, changing lives and bringing new medicines to those who need them.We're seeking a skilled Clinical Research Associate Coordinator to join our international team. As the primary point of contact between site...


  • Xico, México Worldwide Clinical Trials A tiempo completo

    About This OpportunityWe are seeking a skilled Clinical Assessment Technologist to join our team at Worldwide Clinical Trials. This role will be responsible for all aspects of assigned projects, including clinical assessment, training development, and data review.Key ResponsibilitiesAssist in reviewing eCOA/ePRO specifications and engaging in User Acceptance...


  • Xico, México Msd A tiempo completo

    At MSD, we are seeking a seasoned Clinical Research Associate to lead our site management efforts across all phases of clinical research studies. This role demands strong knowledge of regulatory compliance and quality standards to ensure seamless execution.Key Responsibilities:Develop and expand territory for clinical research by identifying new sites and...


  • Xico, México Syneos - Clinical And Corporate - Prod A tiempo completo

    **Clinical Research Associate II Job Summary**Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.**Key Responsibilities**Performs site qualification, site initiation,...


  • Xico, México Icon Plc A tiempo completo

    At ICON Plc, we are a world-leading healthcare intelligence and clinical research organization. Our mission is to shape the future of clinical development.We foster an inclusive environment driving innovation and excellence. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve...


  • Xico, México Icon Plc A tiempo completo

    At ICON, we empower our patients to take an active role in their healthcare journey. We are seeking a highly skilled Clinical Research Associate I to join our team and contribute to our mission of advancing clinical research and improving patient outcomes.The Clinical Research Associate I will be responsible for ensuring the smooth execution of departmental...


  • Xico, México Clinical Trial Network A tiempo completo

    We are seeking a highly skilled Clinical Research Coordinator to join our team at Clinical Trial Network in Houston, Texas.This full-time position offers an exciting opportunity for a motivated individual to work in clinical research and contribute to the planning, implementation, and coordination of studies.Responsibilities:Coordinate and manage all aspects...


  • Xico, México Thermo Fisher Scientific A tiempo completo

    About the RoleAs a Clinical Research Associate at Thermo Fisher Scientific, you will play a vital role in bringing life-changing therapies to market. You will work closely with our clients to define and develop clinical programs, minimize delays, and execute high-quality, cost-efficient clinical studies.As an Assistant CRA (ACRA), your primary responsibility...


  • Xico, México Icon A tiempo completo

    At ICON, we are committed to advancing clinical research and providing outsourced services to pharmaceutical, biotechnology, and medical device organizations. As a Clinical Research Associate, you will play a critical role in ensuring the success of our clients' projects.**Key Responsibilities:** Collaborate with global study teams to ensure timely and...


  • Xico, México Iqvia A tiempo completo

    Job OverviewAs a Clinical Trial Assistant at Iqvia, you will play a crucial role in ensuring a complete and accurate Trial Master File delivery. This involves working closely with the Clinical Research Associates and Regulatory and Start-Up teams to perform daily administrative activities.Key Responsibilities:- Assist Clinical Research Associates and...


  • Xico, México Novasyte A tiempo completo

    Job OverviewAs a Clinical Research Associate at Novasyte, you will be responsible for performing site monitoring visits to ensure compliance with contracted scope of work and regulatory requirements. This includes administering protocol and related study training to assigned sites, establishing regular lines of communication, and evaluating the quality and...


  • Xico, México Thermo Fisher Scientific A tiempo completo

    Job Overview:The Clinical Research Associate - Site Monitoring Specialist is responsible for ensuring the integrity and quality of clinical trial data. This role involves monitoring investigator sites, conducting on-site file reviews, and maintaining effective communication with investigative sites, client companies, and project teams.