Site Manager

**Detalles de la oferta**:
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at
Job Function:
R&D Operations
Job Sub Function:
Clinical Trial Support
Job Category:
Professional
All Job Posting Locations:
Buenos Aires, Argentina
**Job Description**:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at
Remote work options may be considered on a case-by-case basis and if approved by the Company.
We are searching for the best talent for Site Manager to be in Buenos Aires, Argentina.
Purpose:
An Associate, Site Manager is an entry level site management role with typically 0-2 years of experience.
This role serves as the primary contact point between the Sponsor and the Investigational Site.
An Associate, Site Manager is assigned to trial sites to ensure inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations and guidelines from study start-up through to site closure.
The Associate, Site Manager will partner with the Local Trial Manager (LTM), Clinical Trial Assistant (CTA) and TDL (Trial Delivery Leader) to ensure overall site management while performing trial related activities for assigned protocols.
May contribute to process improvement and training.
Some supervision from a more Senior, Site Manager (Senior SM or Lead SM) to help provide guidance to Associate, Site Manager.
You will be responsible for:
Acts as primary local company contact for assigned sites for specific trials.
May participate in site feasibility and/or Site Qualification Visit.
Attends/participates in investigator meetings as needed.
Responsible for executing activities within site initiation and start-up, preparation and conduct of site monitoring (including remote monitoring), site management (by study specific systems and other reports/dashboards) and site/study close-out according to SOPs, Work Instructions (WIs) and policies.
Responsible for the implementation of analytical risk-based monitoring model at the site level and to work with site to ensure timely resolution of issues found during monitoring visits.
Occasionally may require assistance or oversight from Lead, Site Manager or LTM.
Ensures site staff are trained and the corresponding training records are complete and accurate at any point during all trial phases.
Responsible in close collaboration with LTM and central study team for activities during site activation to speed up the process and activate the site in the shortest possible timeframe.
Contributes to site level recruitment strategy and contingency planning and implementation in partnership with other functional areas.
Ensures site study supplies (such as Non-Investigational Product (IP), lab kits, etc.)
are adequate for trial conduct.
Ensures that clinical drug supplies are appropriately used, handled, and stored and returns are accurately inventoried and documented.
Arranges for the appropriate destruction of clinical supplies.
Ensures site staff complete data entry and resolve queries within expected timelines.
Ensures accuracy, validity and completeness of data collected at trial sites.
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.
For AEs/SAEs, ensures that they are consistent with all data collected and with the information in the source documents.
Maintains complete, accurate and timely data and essential documents in relevant systems utilized for trial management.
Fully documents trial related activities, in particular monitoring.
Writes visit reports and follow-up letters in accordance with the SOPs.
Promptly communicates relevant status information and issues to appropriate stakeholders.
Reviews study files for completeness and ensures archiving retention requirements are met, including storage in a secure area at all times.
Collaborates with LTM for documenting and communicating site/study progress and issues to trial central team.
Active participation in regularly scheduled team meetings and trainings.
Provide feedback as appropriate.
May be asked to lead/provide leade