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 https://www.jnj.com
Job Function:
Career Programs
Job Sub Function:
Non-LDP Intern/Co-Op
Job Category:
Career Program
All Job Posting Locations:
Istanbul, Turkey
Job Description:
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, 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
The internship is opened to University students regularly enrolled in the last year of a University course or in their MSc thesis. The internship is 6-months long.
The Clinical Operations intern will support daily documentation activities and quality-related activities for the elements applicable to clinical research, from study start-up phase to study closure.
Activities:
•Support Good Documentation Practices.
•Support administrative and logistical support to Local Trial Manager (LTM) and/or Site Manager (SM) in tracking progress of the trial.
•Support ensuring current versions of the required trial documents, trial-relatedmaterials and supplies are provided to the investigational site within requiredtimeframes, as applicable.
•Support Ethics Committee and Health Authority submissions of necessary documentsand follow up the approval.
•Support maintaining information in relevant systems according to the guidelines.
•Support document filing activities by keeping up with timely filing requirements.
•Support for quality complaint process.
•Maintain good understanding of SOPs and local regulations.
•Comply with all training requirements.
General Activities
•Base all actions on Credo. Protect the rights of others, protect privacy and company assets.
•Work in line with the HCC, company policies and procedures, including SOPs, having the ethical aspect in mind. Comply with ICH-GCP and all applicable local laws and regulations.
•Maintain communication with relevant parties within and outside the company
•Actively follow trainings to ensure adequate qualification
•Regularly update information in applicable systems and templates
•Contribute to maintain quality standards and timelines that are consistent with business needs
•Support activities linked to the reporting of J&J
Requirements:
•Students in Biology / Chemistry / Pharmacy / Molecular Biology & Genetics /Bioengineering or related disciplines
•Full competency in local languages and advance level of English
•Organized, and able to work with people within a company environment and musthave strong communication skills
•Demonstrate high discipline, focus, and analytical thinking
•Skilled in Microsoft Office program use.
Required Skills:
Preferred Skills:
