Clinical Team Lead

2 semanas atrás

Cidade Jardim, Brasil Labcorp Tempo inteiro

The Clinical Team Lead (CTL) is the leader for the clinical team in our Clinical Operations **CTL** group. The Clinical Team Lead (CTL) is responsible and accountable for the execution of the clinical operations component of the project, at the global or regional level, as assigned. The CTL is responsible for working cross functionally, within a matrix environment, to ensure successful execution of the trial including oversight of the clinical operations from a quality, timeline, budget and scope perspective.

**Essential Job Duties**:

- Responsible and accountable for the management of the Clinical Operations team with particular emphasis on teamwork, quality, timelines, budget, metrics and compliance with the project plans and SOPs.
- Develop the strategy, plans, tools and training to oversee and assess performance of the clinical team, in the conduct and compliance of site visits (on site and remote), including, but not limited to: Pre-Study Visits, Site Initiation Visits, Routine Monitoring Visit, Motivational Visits, Close-out Visits, Audit support Visits.
- Proactively communicate with CRAs and other members of the clinical operations team to follow up on all open issues, drive patient recruitment and retention, in order to meet the project timelines.
- Ensure that all study related, clinical related documents are tracked, filed and reviewed (QC check) and complete according to the SOPs, regulatory requirements and protocol.
- Responsible and accountable for understanding and managing the clinical operations budget for the project, and ensure that the activities are within budget and scope of work, and to discuss with the project team to support financial progress, and team utilization.
- Communicate effectively with all members of the project team and client as applicable, to support the study completion per company and client requirements and timelines, including risk identification and mitigation, issue escalation and working with Quality and the project team on Corrective and Preventative Actions.
- As required by the project roles participate and oversee the site selection process. Depending on the scope and roles within the project team, this may be performed in collaboration with other team members.
- As required by the project roles participate and oversee the regulatory/ethics committee submissions, tracking and documentation.
- Support new business with active participation in Bid Defense preparation and meetings, as required.
- Perform other duties as required by the Department or Project Team.

**Education**:

- BSc or BA degree in a biomedical or related life science, or nursing qualification.
- Or an equivalent combination of education and experience to successfully perform the key responsibilities of the job.

**Minimum Required:
- 0-4 years’ experience as a CTL, or an equivalent combination of education and experience to successfully perform the key responsibilities of the job.
- Minimum 4+ years CRA experience, on-site or in-house.

Or

**Labcorp is proud to be an Equal Opportunity Employer**:
As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.

For more information about how we collect and store your personal data, please see our Privacy Statement.

  • Sr Clinical Team Lead

    Há 4 dias

    Cidade Jardim, Brasil Labcorp Tempo inteiro

    **Are you ready to discover you next career Labcorp Drug Development?** **A career at Labcorp provides our employees the unique chance to create an immediate impact and difference in our patient’s lives.** will offer a rewarding career, a chance to work in an energetic & team oriented work place, and access to competitive benefits. With the support of...

  • Clinical Research Team Member

    Há 2 dias

    Cidade Jardim, Brasil beBeeClinicalResearch Tempo inteiro R$86.400 - R$121.800

    Clinical Research Associate JobAre you a detail-oriented and organized professional seeking a challenging role in clinical research? Do you have excellent communication and problem-solving skills? We are looking for a Clinical Research Associate to join our team!The successful candidate will be responsible for monitoring and managing clinical trial sites,...

  • Clinical Research Associate II Role

    Há 5 dias

    Cidade Jardim, Brasil beBeeClinicalResearchAssociate Tempo inteiro US$110.000 - US$130.000

    Job Title: Clinical Research Associate II RoleThis role is responsible for site monitoring, data management and regulatory compliance. The ideal candidate will have a strong background in clinical research, excellent communication skills and the ability to work independently.Responsibilities:- Conduct site initiation and routine visits to ensure study...

  • Senior Clinical Trial Specialist

    Há 4 dias

    Bom Jardim, Brasil beBeeClinical Tempo inteiro US$60.000 - US$80.000

    We are a global Contract Research Organization (CRO) focused on developing and delivering innovative clinical trials.Our goal is to find cures for the world's most persistent diseases through quality excellence and pioneering approaches.Clinical Trials Associates play a vital role in supporting our team in delivering high-quality clinical trials that bring...

  • Global Clinical Project Manager

    Há 4 dias

    Bom Jardim, Brasil beBeeClinical Tempo inteiro R$90.000 - R$134.000

    As a key member of our clinical trial delivery team, you will work closely with clinical teams to improve patients' lives by bringing new treatments to the market faster.Key Responsibilities:Ensure compliance with regulatory requirements and internal standards for assigned projects.Develop effective strategies to meet project targets.Identify and manage...

  • Clinical Research Associate

    Há 3 dias

    Cidade Jardim, Brasil Labcorp Tempo inteiro

    **Essential Job Duties**: 1) Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned 2) Responsible for all aspects of site management as prescribed in the project plans 3)...

  • Snr. Proposal Associate

    2 semanas atrás

    Cidade Jardim, Brasil Labcorp Tempo inteiro

    Recognized as one of Forbes 2021 World’s Best Employers and named in Fast Company magazine’s list of 2021 Most Innovative Companies, LabCorp is seeking a Sr. Proposal Associate to join our Clinical Biotech Proposal Management team. Labcorp Clinical Biotech believes in harnessing science to improve health and the lives of people in need of various...

  • In-house Cra I

    1 semana atrás

    Cidade Jardim, Brasil Labcorp Tempo inteiro

    The In-House Clinical Research Associate (IHCRA I) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the IHCRA I shall reflect their experience, and level of contribution which they can make to the project. The work will involve Clinical Operations activities...

  • Aml Team Lead

    4 semanas atrás

    Bom Jardim, Brasil BM Global Services Buenos Aires Tempo inteiro

    Nos encontramos en la búsqueda de un/a AML/KYC Compliance Team Lead.¿Cuáles serán tus funciones?- Coordinar, asignar y monitorear la carga de trabajo del equipo, garantizando la productividad y el cumplimiento de estándares.- Guiar al equipo en procesos de evaluación de riesgo, validación de clientes y screening de AML/sanciones.- Actuar como...

  • Global Study Leadership

    Há 5 dias

    Bom Jardim, Brasil IQVIA Tempo inteiro

    OverviewAssociate Clinical Leads are an integral part of clinical trial delivery, working alongside clinical teams to improve patients' lives by bringing new drugs to the market faster. The Associate Clinical Lead is a member of the core project team responsible for the clinical delivery of clinical studies to meet contractual requirements in accordance with...