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A leading company in the pharmaceutical sector is seeking a Clinical Trial Assistant to support clinical trials in São Paulo. The role involves managing trial documents, ensuring compliance with regulations, and providing logistical support to trial managers. Ideal candidates will have a degree in Life Sciences and relevant experience in clinical trials.
Join to apply for the Clinical Trial Assistant role at Johnson & Johnson Innovative Medicine
Join to apply for the Clinical Trial Assistant role at Johnson & Johnson Innovative Medicine
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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 https://www.jnj.com
Job Function
R&D Operations
Job Sub Function
Clinical Trial Support
Job Category
Professional
All Job Posting Locations:
São Paulo, Brazil
Job Description
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: https://www.jnj.com/innovative-medicine
We are searching for the best talents for this 1 position of Clinical Trial Assistant (home based).
Purpose: The Clinical Trial Assistant supports the Local Trial Manager (LTM) and/or Site Manager (SM) to ensure optimal management of all documents with logistical and administrative tasks related to trial start-up, execution and closing of clinical trials. Ensures trial related activities are compliant with GCO SOPs, policies and local regulatory requirements. May contribute to process improvement, training and mentoring of other CTAs.
Principal Responsibilities
1 Provide administrative and logistical support to LTM and/or SM in tracking progress of the trial, management of study data, budget, organizing meetings, mailing and correspondence, materials, drug distribution and other relevant tasks as appropriate in adherence to relevant SOPs, policies and local regulatory requirements.
2 Supports the local study team in performing site feasibility and/or country feasibility.
3 Maintains information in relevant systems.
4 Ensures current versions of the required trial documents, trial-related materials and supplies are provided to the investigational site within required timeframes, as applicable.
5 Support LTM and/or SM in collecting/preparing documents required for study startup/submission to IEC/IRB and/or HA.
6 Support LTM and/or SM in collecting, processing and archiving study related documents as appropriate. Use appropriate systems to ensure file completeness at designated study milestones.
7 May assist LTM in conducting local investigator meeting or with making arrangements for the investigators participating in an international meeting.
8 Maintains and updates contact information in relevant systems to ensure appropriate safety updates distribution.
9 Comply with all training requirements
10 Ensure inspection readiness at all times.
11 May contribute to process improvement including, but not limited, to representing functional area in process initiatives and contribute to optimization of daily processes.
12 May be assigned as a coach and mentor to a less experienced CTA.
Education And Experience Requirements
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