Empleos actuales relacionados con Senior Clinical Research Associate - Munro - MSD

  • Sr. Clinical Research Associate

    hace 2 semanas

    Munro, Argentina MSD A tiempo completo

    Are you an experienced Clinical Research Associate looking for a new opportunity to excel in your career? Join our dynamic team and make a difference in the field of clinical research. We are seeking a highly motivated and detail-oriented individual to oversee and manage clinical research protocols and sites in Argentina. As a Clinical Research Associate,...

  • Clinical Research Associate

    hace 2 meses

    Munro, Argentina MSD A tiempo completo

    Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us. Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and...

  • Clinical Research Manager

    hace 5 meses

    Munro, Argentina MSD A tiempo completo

    Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where our company has codified its 125-year legacy. Our company success is backed by ethical...

  • Clinical Operation Manager Com-financial

    hace 5 meses

    Munro, Argentina MSD A tiempo completo

    Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine. This role is accountable for performance and compliance for assigned...

  • Clinical Operations Manager

    hace 5 meses

    Munro, Argentina MSD A tiempo completo

    Join us in our mission to INVENT the future. Let’s be part of our team of dedicated, energetic individuals who are committed to be the most trusted supplier of pharmaceuticals and health products worldwide. **Key Responsibilities** PERFORMANCE & COMPLIANCE - Accountable for execution and oversight of local operational clinical trial activities in a...

  • Data Management Trial Manager

    hace 5 meses

    Munro, Argentina MSD A tiempo completo

    Position Overview: The Trial Manager creates and ensures the successful execution of the clinical data management strategy for assigned trials within a specific drug/vaccine program. Develops and manages project plans which span from protocol development through database lock, archiving, and submission deliverables where applicable. Collaborates with...

  • (Finance) Clinical Trial Coordinator

    hace 1 mes

    Munro, Argentina MSD A tiempo completo

    Under the oversight of the line-manager, this role is responsible for comprehensive trial and site administration and involves preparing, collating, distributing and archiving clinical documents. The role is critical to meet planned Site Ready dates. The role will collaborate at local level closely with COM, CRM and CRA. And the person collaborates with...

  • Cra

    hace 5 meses

    Munro, Argentina MSD A tiempo completo

    The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations, company´s policies and procedures, quality standards and adverse event reporting requirements internally and externally. Acts as...

  • Sr. Cra

    hace 6 meses

    Munro, Argentina MSD A tiempo completo

    The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager or CRD, the person ensures compliance of study conduct with ICH/GCP and country regulations, company policies and procedures, quality standards and adverse event reporting requirements internally and externally. Acts...

  • Cra

    hace 7 meses

    Munro, Argentina MSD A tiempo completo

    The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations, company´s policies and procedures, quality standards and adverse event reporting requirements internally and externally. Acts as...

  • Msl General Medicine

    hace 5 meses

    Munro, Argentina MSD A tiempo completo

    Medical Science Liaison Specialist (MSL Specialist) is a credentialed therapeutic and disease expert who engages in scientific exchange with leaders in the external medical and scientific community. The role provides scientific leaders (SLs) balanced, factual, scientific information about non-product areas of interest to the Company and replies to scientific...

  • Cra Junior

    hace 4 meses

    Munro, Argentina MSD A tiempo completo

    With support of SrCRA/CRA and/or CRA Manager, acts as primary site contact and site manager throughout all phases of a clinical research study, taking responsibility of allocated sites. - Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. - Performs clinical study site management/monitoring...

  • Cra Junior

    hace 5 meses

    Munro, Argentina MSD A tiempo completo

    With support of SrCRA/CRA and/or CRA Manager, acts as primary site contact and site manager throughout all phases of a clinical research study, taking responsibility of allocated sites. - Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. - Performs clinical study site management/monitoring...

  • Cra Junior

    hace 1 mes

    Munro, Argentina MSD A tiempo completo

    With support of SrCRA/CRA and/or CRA Manager, acts as primary site contact and site manager throughout all phases of a clinical research study, taking responsibility of allocated sites. - Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. - Performs clinical study site management/monitoring...

  • Medical Science Liaison Oncology

    hace 5 meses

    Munro, Argentina Bayer A tiempo completo

    **Bayer es una compañía global con competencias centradas en los campos de las ciencias de la vida de la salud y la agricultura. Sus productos y servicios están diseñados para beneficiar a las personas y mejorar su calidad de vida. En Bayer tienes la oportunidad de ser parte de una cultura en la que valoramos la pasión de nuestros colaboradores por...

  • Medical Science Liaison Oftalmology

    hace 5 meses

    Munro, Argentina Bayer A tiempo completo

    **Bayer es una compañía global con competencias centradas en los campos de las ciencias de la vida de la salud y la agricultura. Sus productos y servicios están diseñados para beneficiar a las personas y mejorar su calidad de vida. En Bayer tienes la oportunidad de ser parte de una cultura en la que valoramos la pasión de nuestros colaboradores por...

  • Cra Manager

    hace 1 semana

    Munro, Argentina MSD A tiempo completo

    This role will be key to ensure strong monitoring in our clinical trials. Under the oversight of the Clinical Research Director, the person is responsible to manage a team of 6-14 CRAs and to ensure excellent study and site performance with strict adherence to local regulations, company SOPs and ICH GCP. As line manager the role is critical to continuously...

  • Cra Manager

    hace 5 meses

    Munro, Argentina MSD A tiempo completo

    This role will be key to ensure strong monitoring in our clinical trials. Under the oversight of the CRD or Head of Site Management and Monitoring, the person is responsible to manage a team of 6-14 CRAs and to ensure excellent study and site performance with strict adherence to local regulations, company SOPs and ICH GCP. As line manager the role is...

  • Medical Science Liaison Oftalmology

    hace 5 meses

    Munro, Argentina Bayer A tiempo completo

    Bayer es una compañía global con competencias centradas en los campos de las ciencias de la vida de la salud y la agricultura. Sus productos y servicios están diseñados para beneficiar a las personas y mejorar su calidad de vida. En Bayer tienes la oportunidad de ser parte de una cultura en la que valoramos la pasión de nuestros colaboradores por...

  • Medical Science Liaison Oncology

    hace 5 meses

    Munro, Argentina Bayer A tiempo completo

    Bayer es una compañía global con competencias centradas en los campos de las ciencias de la vida de la salud y la agricultura. Sus productos y servicios están diseñados para beneficiar a las personas y mejorar su calidad de vida. En Bayer tienes la oportunidad de ser parte de una cultura en la que valoramos la pasión de nuestros colaboradores por...

Senior Clinical Research Associate

hace 3 meses

Munro, Argentina MSD A tiempo completo

Job Description

Are you an experienced Clinical Research Associate looking for a new opportunity to excel in your career? Join our dynamic team and make a difference in the field of clinical research. We are seeking a highly motivated and detail-oriented individual to oversee and manage clinical research protocols and sites in Argentina. As a Clinical Research Associate, you will play a crucial role in ensuring compliance with regulations, company policies, and quality standards.

 

Responsibilities:

  • Develop strong site relationships and ensure continuity throughout all phases of the trial.

  • Perform clinical study site management activities in compliance with ICH-GCP, Sponsor SOPs, local laws & regulations, and protocol requirements.

  • Gain in-depth understanding of study protocols and related procedures.

  • Coordinate and manage tasks in collaboration with other sponsor roles to achieve site readiness.

  • Conduct remote and on-site monitoring activities to ensure data accuracy and subjects' safety.

  • Collect, review, and monitor regulatory documentation for study start-up, maintenance, and close-out.

  • Communicate with investigators and site staff on protocol conduct, recruitment, retention, and regulatory compliance.

  • Identify and resolve site performance, quality, or compliance issues in collaboration with relevant stakeholders.

  • Work collaboratively with internal teams and external partners in support of assigned sites.

  • Manage and maintain information and documentation in various systems.

  • Contribute to CRA team knowledge by acting as a subject matter expert, sharing best practices, and providing training as needed.

  • Support audit and inspection activities as required.

  • Contribute to the identification and development of new potential sites.

 

Requirements:

  • Minimum 4 years of direct site management (monitoring) experience in bio/pharma/CRO.

  • Fluent in local languages and English (verbal and written) with excellent communication skills.

  • Excellent understanding of clinical research, GCP/ICH guidelines, and country-specific regulations.

  • Demonstrated ability to mentor and lead.

  • Strong IT skills and ability to adapt to new applications.

  • Ability to analyze data/metrics and take appropriate action.

  • Experience with site motivational visits to boost enrollment.

  • Capable of managing complex issues and implementing corrective action.

  • B.A./B.S. with strong emphasis in science and/or biology preferred.

 

Why Join Our Team:

  • Opportunity to work in a dynamic and growing company at the forefront of clinical research.

  • Collaborative and supportive work environment.

  • Growth and development opportunities.

  • Competitive salary and benefits package.

  • Don't miss this chance to take your career to the next level. Apply now and be part of our team

 

Current Employees apply HERE

Current Contingent Workers apply HERE

Search Firm Representatives Please Read Carefully 
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company.  No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. 

Employee Status:

Regular

Relocation:

No relocation

VISA Sponsorship:

No

Travel Requirements:

No Travel Required

Flexible Work Arrangements:

Hybrid

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

N/A

Job Posting End Date:

08/30/2024

*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.


Job Posting End Date:08/30/2024


A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.


Requisition ID:R268733