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Local Trial Manager

Local Trial Manager
Empresa:

Johnson & Johnson


Detalles de la oferta

Local Trial Manager

At Johnson & Johnson, the largest healthcare company in the world, we come together with one purpose: to profoundly change the trajectory of health for humanity.

Diversity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years. Regardless of your race, belief, sexual orientation, religion or any other trait, YOU are welcome in all open positions at the largest healthcare company in the world.

When You Join Johnson & Johnson, Your Next Move Could Mean Our Next Breakthrough.

If you're passionate about your career every single day, we'd love to hear from you!

We invite you to read this Job Description and apply if you are passionate about the position and meet the requirements.

The Janssen Pharmaceutical Companies of Johnson & Johnson are dedicated to addressing and solving the most important unmet medical needs of our time, including oncology (e.g., multiple myeloma and prostate cancer), immunology (e.g., rheumatoid arthritis, irritable bowel disease and psoriasis), neuroscience (e.g., schizophrenia, dementia and pain), infectious disease (e.g., HIV/AIDS, Hepatitis C and tuberculosis), cardiovascular and metabolic diseases (e.g., diabetes) and Pulmonary Arterial Hypertension (PAH) and Rare Diseases.

The Local Trial Manager is responsible for local management of a clinical trial (or Medical Affairs data generation activity) in a country or countries. The LTM is the primary point of contact at a country level for assigned studies and has operational oversight of assigned protocol(s) from start-up through to database lock and closeout activities as described in GCO procedural documents. The LTM is responsible for coordinating and leading the local trial team to deliver quality data and trial documents/records that are compliant with the assigned clinical trial protocol, company Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and regulatory requirements. The LTM role actively leads or contributes to process improvement; training and mentoring of other LTM s and Site Managers (SM).

Main Responsibilities:

1. Collaborate with Functional Manager (FM)/Clinical Research Manager (CRM) for country protocol feasibility and site feasibility assessment. Implements any local criteria for site selection. Ensure consistent conduct of pre-trial assessment visits and instruct teams on appropriate follow-up of pre-trial visit report and country feasibility report. Recommends suitable sites for selection to participate in trial.

2. Collaborates with the Global and Local management team.

3. Contributes input to the study management documents at a country level or initiates development of these documents for a single country trial, as per SOPs

4. Leads and coordinates local trial team activities in compliance with SOPs, other procedural documents and applicable regulations. Leads local project planning activities to meet recruitment targets and to deliver high quality data on time and within study budget. Including but not limited to: development of local trial specific procedures and tools, recruitment planning, contingency and risk management, and budget forecasting.

5. Ensures that all Adverse Events (AE) /Serious Adverse Events (SAEs)/Product Quality Complaints (PQCs) are reported within the required reporting timelines and documented as appropriate.

6. Maintains and updates trial management systems. Uses study tools and management reports available to analyse trial progress

7. Monitors country progress and initiates corrective and preventive actions (CAPA) when the trial deviates from plans and communicates study progress and issues to study management teams.

8. May submit requests for vendor services and may support vendor selection.

9. In certain situations, may assist in negotiation of trial site contracts and budgets. Forecasts and manages country/local trial budget to ensure accurate finance reporting and trial delivered –within budget. Adheres to finance reporting deliverables and timelines.

10. Attends/participates in Investigator Meetings as needed. May schedule and conduct a local/country investigator meeting

11. Conducts local trial team meetings and provides or facilitates SM training when needed (i.e. implementation of study amendment-and changes in study related processes).

12. Reviews and approves Monitoring Visit Reports submitted by SM; identifies issues and/or trends across a trial project and escalates deviation issues to the CTM/GTL and FM as needed

13. Reviews and approves site and local vendor invoices as required. Manages local study supply, as required.

14. Prepares country specific informed consent in accordance with procedural document/templates. Reviews and manages site specific informed consent forms in accordance with SOPs, other procedural documents and applicable regulations.

15. Organizes and ensures IEC/HA approvals, if applicable, and ensure that the trial is in compliance with local regulatory requirements.

16. Works with SM to ensure CAPA is implemented for audits and inspection or any quality related visits

17. Complies with relevant training requirements.

18. Acts as subject matter expert for assigned protocols. Develops strong therapeutic knowledge to support roles and responsibilities. May represent GCO on cross functional teams.

19. Acts as primary local/country contact for a trial. Establishes and maintains excellent working relationships with external stakeholders, in particular investigators, study trial coordinators and other site staff; and internal stakeholders, including Medical Affairs and Marketing for Medical Affairs trials.

20. Actively leads or contributes to process improvement, training and mentoring of CTAs, SM and other LTMs.

21. Conducts accompanied site visits with SM as delegated by FM.

22. Assumes additional responsibilities or special initiatives such as “Champion” or “Subject Matter Expert”.

23. Represents functional area in process initiatives as required

Qualifications
Educational Background: A minimum of a BA or BS degree in Life Sciences, Nursing or related scientific field (or equivalent experience) is required. Years of experience: Minimum of 4 years of pharmaceutical and/or clinical trial experience is preferred (including site monitoring experience), Experience: Specific therapeutic area experience may be required depending on the position; Strong experience in mentoring/coaching and providing training to other LTMs, SMs and CTAs. Knowledge required: have solid understanding of the drug development process including GCP and local regulatory requirements. Skills: Strong leadership skills; Demonstrated ability to lead initiative/small teams; Flexible mindset and ability to work in a fast-changing environment. Ability to work on multiple trials in parallel in different disease areas, if required. Language: Proficient in speaking and writing the country language and English language. Location of the role: Buenos Aires, Argentina.


Fuente: Whatjobs

Requisitos


Conocimientos:
Local Trial Manager
Empresa:

Johnson & Johnson


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