Sr Clinical Trial Coord

hace 2 semanas

Buenos Aires, Argentina PPD A tiempo completo

**JOB DESCRIPTION**:

- We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving therapies to patients.
Our global Clinical department consists of colleagues with institutional knowledge, in-depth therapeutic experience, and robust operational tools. Together, we help clients define and develop clinical programs, minimize delays and execute high-quality, cost-efficient clinical studies.
As a PPD Clinical Trial Coordinator you will provide administrative and technical support to the Project Team. You will support audit readiness by ensuring files are reviewed on schedule detailed in the organization's WPD and department guidance document.
At PPD we hire the best, develop ourselves and each other, and recognize the power of being one team. We offer continued career advancement opportunities, award winning training and benefits focused on the health and wellbeing of our employees.
Summarized Purpose:
Provides administrative and technical support to the Project Team. Coordinates and facilitates project activities and may serve as a study lead acting as a cross-functional liason for the project team. Acts as a buddy during onboarding phase and provides training to new staff as needed. Supports departmental and cross-functional initiatives for process improvements/enhancements.
Essential Functions:

- According to the specific role (Central or Local), coordinates, oversees and completes functions on assigned trials activities detailed on the task matrix.
- Performs department, Internal, Country and Investigator file reviews as assigned and documents findings in appropriate system.
- Ensures allocated tasks are performed on time, within budget and to a high-quality standard. Proactively communicates any risks to project leads and line manager as appropriate.
- Supports the maintenance of study specific documentation and global support with specific systems, tools and trackers including but not limited to: study team lists, tracking of project specific training requirements, system access management for organization/vendor/clients, and tracking of project level activity plans in appropriate system. Ensures (e)TMF is up to date by following file review schedules and documents findings in appropriate system.
- Provides system support (i.e. GoBalto & eTMF).
- Supports RBM activities.
- Performs administrative tasks on assigned trials including but not limited to: timely processing of documents sent to Client (e)TMF as assigned, performing (e)TMF reviews, performing mass mailings and communications as needed, providing documents and reports to internal team members.
- Supports scheduling of client and/or internal meetings with completion of related meeting minutes.
- Reviews and tracks local regulatory documents.
- Transmits documents to client and centralized IRB/IEC.
- Analyzes and reconciles study metrics and findings reports. Assists with clarification and resolution of findings related to site documentation.
- Maintains vendor trackers.
- Assists with coordination, compilation and distribution of Investigator Site File (ISF) and Pharmacy binder materials and non-clinical study supplies to sites.
- Assists with study-specific translation materials and translation QC upon request.
- May attend Kick off meeting and take notes when required.

**Job Qualification**:

- Education and Experience:
High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification.
Bachelor's degree preferred.
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to at least 4 years).
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Knowledge, Skills and Abilities:

- Ability to work in a team or independently as required
- Strong organizational skills and attention to detail, with proven ability to handle multiple tasks efficiently and effectively
- Proven ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency
- Strong customer focus
- Demonstrated flexibility and adaptability to reprioritize workload and provide efficient support to meet changing project timelines
- Demonstrated ability to attain and maintain a good working knowledge of applicable Country Regulations, ICH Good Clinical Practices, and organization/Client SOPs and WPDs for all non-clinical/clinical aspects of project implementation, execution and closeout
- Excellent English language and grammar skills and proficient local language skills as needed
- Good presentation skills
- Excellent compu

  • Clinical Trial Coord

    hace 4 semanas

    Buenos Aires, Argentina Thermo Fisher Scientific A tiempo completo

    Our team of colleagues in clinical research services are at the forefront of getting cures to market. We bring a high caliber of scientific and clinical expertise to the development of drugs that address the world’s most challenging health concerns. Our Clinical Research team, who powers our PPD® clinical research portfolio, are part of our leading global...

  • Clinical Trial Coord

    hace 4 semanas

    Buenos Aires, Argentina Thermo Fisher Scientific A tiempo completo

    We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving...

  • Clinical Trial Coord

    hace 4 semanas

    Buenos Aires, Argentina PPD A tiempo completo

    **JOB DESCRIPTION**: - We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of...

  • Sr Clinical Trial Coord

    hace 1 semana

    Buenos Aires, Argentina PPD A tiempo completo

    We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving...

  • Clinical Trial Operations Lead

    hace 1 día

    Buenos Aires, Buenos Aires C.F., Argentina IQVIA A tiempo completo

    Clinical Trial Operations LeadWe are seeking a seasoned professional to lead our clinical trial operations team. As a Clinical Trial Operations Lead, you will be responsible for overseeing the planning, execution, and delivery of clinical trials.Key Responsibilities:Develop and execute operational strategies for clinical trialsCollaborate with...

  • Clinical Trial Site Engagement Sr Manager

    hace 1 semana

    Buenos Aires, Argentina Amgen A tiempo completo

    Career Category Clinical **Job Description**: Clinical Trial Site Engagement Sr Manager Develop, implement and maintain an integrated site engagement and operational role at key/targeted sites in line with Global Development pipeline to support strategic global study strategy plan to accelerate development of marketed products and early pipeline assets....

  • Clinical Trial Site Engagement Sr Manager

    hace 1 semana

    Buenos Aires, Argentina Amgen A tiempo completo

    Clinical Trial Site Engagement Sr Manager Develop, implement and maintain an integrated site engagement and operational role at key/targeted sites in line with Global Development pipeline to support strategic global study strategy plan to accelerate development of marketed products and early pipeline assets. Maintains an effective collaborative partnership...

  • Clinical Trial Optimization Specialist

    hace 5 días

    Buenos Aires, Buenos Aires C.F., Argentina Zs Associates A tiempo completo

    ZS Associates is a leading provider of clinical trial optimization solutions, partnering with pharmaceutical companies to improve trial efficiency and effectiveness.We're seeking an experienced Clinical Trial Optimization Specialist to join our team and contribute to delivering cutting-edge solutions that drive business growth and...

  • Senior Clinical Trial Coordinator

    hace 4 días

    Buenos Aires, Buenos Aires C.F., Argentina Avature A tiempo completo

    Responsibilities:The Clinical Team Lead will be responsible for leading clinical trials in the LATAM region, working closely with cross-functional teams to ensure successful trial execution. Key responsibilities include:Selecting sites, conducting and delivering trials according to the clinical trial protocol.Adapting required documents for submission and...

  • Clinical Trial Coord Ii

    hace 4 semanas

    Buenos Aires, Argentina Thermo Fisher Scientific A tiempo completo

    We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving...

  • Clinical Trial Coord Ii

    hace 2 semanas

    Buenos Aires, Argentina Thermo Fisher Scientific A tiempo completo

    We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving...

  • Clinical Trial Coordinator

    hace 2 días

    Buenos Aires, Buenos Aires C.F., Argentina IQVIA Argentina A tiempo completo

    Clinical Trials CoordinationWe are looking for a talented Clinical Trial Coordinator to support our clinical trials operations at IQVIA Argentina. In this role, you will work closely with internal stakeholders and external partners to set up studies and data integrations within sample tracking software systems.Key FunctionsAssist in the development of...

  • Senior Clinical Trial Manager

    hace 3 días

    Buenos Aires, Buenos Aires C.F., Argentina 4Peeq A tiempo completo

    About UsAt 4Peeq, we are passionate about improving patient outcomes through innovative clinical trials. We are seeking an experienced Clinical Trial Liaison Director to join our team and lead a team of Clinical Trial Ambassadors across LATAM.Main ResponsibilitiesDevelop and implement strategies to improve patient recruitment and retentionLead a team of...

  • Clinical Trial Ambassador Director

    hace 3 días

    Buenos Aires, Buenos Aires C.F., Argentina 4Peeq A tiempo completo

    Role OverviewThe Clinical Trial Liaison Director will play a pivotal role in leading a team of Clinical Trial Ambassadors across LATAM, focusing on patient identification, enrollment, and retention in clinical trials.This position requires a strong leader who can develop and implement trial site feasibility support and potential referral sites specific...

  • Clinical Trial Manager

    hace 1 semana

    Buenos Aires, Argentina Icon plc 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 fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery,...

  • Clinical Trial Educator

    hace 2 semanas

    Buenos Aires, Argentina IQVIA A tiempo completo

    **Job Overview** The Clinical Trial Educator (CTE) will provide information and education on clinical trial inclusion and exclusion criteria to trial coordinators and healthcare providers. The Clinical Trial Educator will provide in-service presentations with the goal to increase patient enrollment. The CTE works in partnership with CRAs and other...

  • Clinical Trial Assistant, Cfsp

    hace 3 semanas

    Buenos Aires, Argentina IQVIA A tiempo completo

    **Job Overview** Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. **Essential Functions** - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining...

  • Sr. Trial Capabilities

    hace 1 semana

    Buenos Aires, Argentina Lilly A tiempo completo

    At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities...

  • Clinical Trial Recruitment Specialist

    hace 3 días

    Buenos Aires, Buenos Aires C.F., Argentina Lot Squared Development A tiempo completo

    About the RoleLotsquared Development is seeking a highly motivated Clinical Trial Recruitment Specialist to join our team. In this critical role, you will be responsible for implementing and delivering effective patient recruitment strategies that drive successful clinical trial outcomes.You will work closely with our clients and internal stakeholders to...

  • Global Clinical Trial Assistant

    hace 3 semanas

    Buenos Aires, Argentina Emprego AR A tiempo completo

    Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. **Essential Functions**: - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining...