Oferty pracy

Nazwa firmy / instytucji

Johnson&Johnson

Adres

Iłżecka24
02-135 Warszawa

Nazwa stanowiska

Global Trial Associate (GTA)-Global Clinical Operations Leadership Development Program 2025

Liczba osób

2

Termin składania podań

30.04.2025

Branża

Lekarz/Farmaceuta/Weterynarz

Charakter pracy

stała

Lokalizacja

Polska

Wymagania

The Global Clinical Operations Department

of Johnson & Johnson conducts clinical trials at various sites

across Poland in therapeutic areas, including but not limited to

oncology, hematology, immunology, cardiology, metabolic diseases,

neurology, and ophthalmology.

We are seeking talented individuals interested in the field of clinical

research to participate in the Global Clinical Operations Leadership

Development Program (GCOLDP).

Criteria & Requirements:

• Must be graduating no more than 12 months prior to the target start date of July

2025, with Master’s degree (MSc) or doctoral students (PhD).

• Excellent organizational skills with the ability to collaborate and manage multiple

priorities within a matrix environment.

• Strong verbal and written communication and presentation skills; knowledge of

MS Excel is preferred.

• Strong interpersonal, leadership, and negotiation skills.

• Ability to speak the local language of the hiring country.

 

• Fluency in Polish and English.

Opis wykonywanych zadań

Principal Responsibilities:

 

• Provide administrative and logistical support to Clinical Trial Assistant (CTAs), SM and/or LTM 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.
• Support the local study team in performing site feasibility and/or country feasibility. Collaborates with the Global Project Team, e.g. Clinical Trial Manager (CTM)/Global Trial Lead (GTL), local management/Country Head and other study team members, as required.
• Maintain information in relevant systems, including electronic filing (electronic Trial Master File: eTMF).
• Ensure current versions of the required trial documents, trial-related materials and supplies are provided to the investigational site within required timeframes, as applicable.
• Support CTA, SM and/or LTM in collecting/preparing documents required for study start-up/ submission to Ethics Committee/IRB and/or Health Authorities.
• Support CTA SM and/or LTM in collecting, processing, and archiving study related documents as appropriate. Use appropriate systems to ensure file completeness at designated study milestones.
• May assist team in conducting local investigator meeting or with planning for the investigators participating in an international meeting.
• Maintain and update contact information in relevant systems to ensure appropriate safety updates distribution.
• Comply with all training requirements, company policies & procedures and all applicable laws and regulations. Always act aligned with J&J Credo.
• Ensure inspection readiness at all times.
• May contribute to process improvement.
• Support SM and within a reasonable timeframe be able to take on responsibility in 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 Standard Operating Procedures, Work Instructions (WIs) and policies.

Warunki zatrudnienia

As part of the internship, we offer:

• A one-year rotational program consisting of dynamic rotations with comprehensive

training in the roles of Clinical Trial Associate, Site Manager, and Local Trial

Manager, supported by strong line management, formal mentorship, sponsorship,

networking opportunities, focused leadership development, and dynamic real-world

work experience.

• T he program provides an unparalleled opportunity to develop an understanding

of pharmaceutical development, regulations, compliance, and patient safety.

• Placement in a Local Trial Manager, Site Manager, or equivalent role upon

successful completion of the rotational program.

• Opportunities to build strong relationships within the global cohort of Global

Trial Associates, as well as exposure to senior leaders within the Global Clinical

Operations organization.

We offer a full-time paid job with an intention of hiring

after 1-year rotational development program.

Salary details will be provided upon application.

Sposób kontaktowania

Interested candidates for this position are invited to apply via the web page: https://flows.beamery.com/jnj/festiwal-mozliwosci-medyczne-targi-pracy-9th-april-2025-npfbt_xa0e or through LinkedIn: https://www.linkedin.com/jobs/view/4198060921

Osoba do kontaktu

Weronika Filipek