Clinical Study Planning Senior Associate Manager

hace 2 semanas

Desde casa, México Parexel A tiempo completo

External Job Description**Responsibilities**:- Lead the development of realistic study timelines, from design through final study reporting on priority programs- Maintaining accuracy of clinical study timeline information in Company data control systems (e.g., Planisware (PPM)- Tracking, documenting, and ensuring key stakeholder involvement and timely delivery of clinical study deliverables- Leading special projects as assigned- Represent Clinical Study Planning group in applicable forums and lead functional specific communications- Closely support Sr. Manager with Program oversight and stakeholder management, as required by the assigned program/s- Oversight of Clinical Study Planning staff, as required by the Sr. Manager- Develop and monitor clinical trial timelines: Ensure high-quality, realistic, cross-functional, global timelines within specified deadlines.- Conduct routine integrity checks: Regularly resolve data issues for assigned study timelines.- Manage, communicate & implement changes- Align funding and investment: Support operational planning by ensuring alignment of funding for clinical studies.- Collaborate and improve: Maintain strong relationships with study teams, identify bottlenecks, and contribute to continuous improvement in project management.**Qualifications**:- Master’s degree & 3 years of directly related experience or Bachelor’s degree & 5 years of directly related experience**Preferred Qualifications**:- BA/BS/BSc in the sciences or RN- 5 years work experience in life sciences or medically related field, including 4 years of biopharmaceutical clinical product development (clinical research or clinical operations experience obtained at a biotech, pharmaceutical or CRO company)- Minimum 3 years’ experience in Clinical Study Planning Manager role- PMP Certification- Drug development knowledge with understanding of other functions, including Pre-Clinical, Clinical, Development Operations, and Regulatory- Project management tools and processes (e.g., MS Project, PPM, PowerPoint, Excel)- Strong communication skills to all levelsLI-REMOTEBack to nav

  • Senior Clinical Research Associate

    hace 2 semanas

    Desde casa, México IQVIA A tiempo completo

    **BASIC FUNCTIONS**:Participates in the preparation and execution of Phase I-IV clinical trials. Oversees the progress of clinical investigations by conducting site evaluation, initiation, and interim close out visits to sites. Monitors clinical trials in accordance with Good Clinical Practices and procedures set forth by IQVIA Biotech and sponsors. Works...

  • Senior Clinical Associate

    hace 2 días

    Desde casa, México ICON A tiempo completo

    ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development...

  • Senior Study Manager

    hace 2 semanas

    Desde casa, México Parexel A tiempo completo

    **Senior Study Manager****Position Purpose**:- The Senior Study Manager (SSM) has responsibility for one or more studies of moderate complexity generally with responsibility for all study management aspects of assigned studies- The SSM leads and manages the tactical execution of one or more clinical studies from study startup through database release and...

  • Clinical Associate

    hace 7 días

    Desde casa, México ICON A tiempo completo

    At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfill our mission to advance and improve patients' lives.ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research by providing outsourced...

  • Clinical Study Team Assistant I

    hace 2 semanas

    Desde casa, México Parexel A tiempo completo

    Parexel is looking for multiple Clinical Study Team Assistant I in Mexico, Argentina or Brazil! The Clinical Study Team Assistant I (CSTA I) is an essential part of the study team and is responsible for supporting key clinical trial tasks for assigned studies to ensure compliance with timelines, Good Clinical Practice (GCP), and client Standard Operating...

  • Clinical Study Team Assistant I

    hace 2 semanas

    Desde casa, México Parexel A tiempo completo

    The Clinical Study Team Assistant I (CSTA I) is an essential part of the study team and is responsible for supporting key clinical trial tasks for assigned studies to ensure compliance with timelines, Good Clinical Practice (GCP), and client Standard Operating Procedures (SOPs). The role collaborates with global study team members and is responsible for...

  • Clinical Trial Manager

    hace 1 semana

    Desde casa, México ICON A tiempo completo

    We are currently seeking a Manager, CTM (Clinical Trial Management) to join our diverse and dynamic team. As the Manager of CTM at ICON, you will play a pivotal role in overseeing the planning and execution of clinical trials, ensuring that they are conducted efficiently and in compliance with regulatory standards. Your leadership will be crucial in driving...

  • Clinical Associate

    hace 2 días

    Desde casa, México ICON A tiempo completo

    ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development...

  • Study Start Up Associate Ii

    hace 2 semanas

    Desde casa, México ICON A tiempo completo

    Study Start Up Associate (Informed Consent)At ICON, it’s our people that set us apart.As a global provider of drug development solutions, our work is serious business. But that doesn’t mean you can’t have fun while you do it. With our vision to be the partner of choice in drug development, we hire only the best and brightest in the industry. Are you...

  • Clinical Research Associate

    hace 1 semana

    Desde casa, México Parexel A tiempo completo

    Parexel is looking for multiple **CRAs** with 1+ year of experience in Mexico! The **Clinical Research Associate**will be responsible for data integrity, data quality and ensuring compliance with ICH GCP and local requirements at the site level. Monitoring will be conducted in line with the Study Monitoring Plan and will be performed virtually for the...