Johnson & Johnson Services, Inc. is recruiting for a SENIOR SITE MANAGER to be located in ISTANBUL. Caring for the world, one person at a time has inspired and united the people of Johnson & Johnson for over 125 years.
We embrace research and science bringing innovative ideas, products and services to advance the health and well-being of people.
Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world.
With $70.1 billion in 2015 sales, Johnson & Johnson is the world's most comprehensive and broadly based manufacturer of health care products, as well as a provider of related services, for the consumer, pharmaceutical, and medical devices and diagnostics markets.
There are more than 265 Johnson & Johnson operating companies employing approximately 126,500 people and with products touching the lives of over a billion people every day, throughout the world.
Thriving on a diverse company culture, celebrating the uniqueness of our employees and committed to inclusion. Proud to be an equal opportunity employer.
And our culture is interconnected by the shared values of Our Credo . It’s a culture that celebrates diversity and diverse perspectives.
It helps employees achieve an effective mix between work and home life and supports their efforts to have a positive impact on their communities.
Summary of the job : A Site Manager is the person in Trial Co-ordination and Site Management that serves as a primary contact point between the sponsor and the investigational site.
A Site Manager is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-
up through data-base lock. Responsibilities include site selection, pretrial assessment, subject recruitment and retention planning, site initiation, monitoring and close-
out. Partner with the CTA / IDA, LTM and GTM to ensure overall site management while performing trial related activities for assigned protocols.
May contribute to process improvement and training Duties & Responsibilities
out according to internal SOPs / WIs / IFUs and policies.
Complete follow-up letter to communicate relevant information and required corrective action to the investigator and his / her team with 15 working days.
Promptly communicates relevant status information and issues to appropriate stakeholders.
A minimum of a BA / BS degree is required. A degree in a health or science related field is preferred, however, other relevant experiences and skills may be considered by the hiring manager when considering the candidate’s eligibility.
A minimum of 3 years of clinical trial monitoring experience is preferred, however, other relevant experiences and skills may be considered by the hiring manager when considering the candidate’s eligibility.
Good working knowledge of ICH-GCP, company standard operating procedures, local laws and regulations, assigned protocols and associated protocol specific procedures including monitoring guidelines.
Good IT skills in appropriate software and company systems. Willingness to travel with occasional overnight stay away from home.
Proficient in speaking and writing the country language and English. Good written and oral communication skills.