Clinical Operations Intern

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 jnj.com .

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world.

We provide an inclusive work environment where each person is considered as an individual.

At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

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 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/ .

We are searching for 2 interns for our clinical operations team located in Istanbul.

As a Clinical Operations Intern, you will support daily documentation activities and quality-related activities for the elements applicable to clinical research, from study start-up phase to study closure.

Internships are open to students attending the 5th or 6th year at university.

Please note that internship is at least 3 days per week for a 6 months period.

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-related

materials and supplies are provided to the investigational site within required

timeframes, as applicable.

• Support Ethics Committee and Health Authority submissions of necessary documents

and 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 and maintain good understanding of SOPs and local regulations.

Qualifications

-Currently pursuing a degree in Pharmacy, Molecular Biology & Genetics /Medicine, Life Sciences, or a related field.
-Full competency in local languages and advance level of English Organized, and able to work with people within a...