Clinical Research Manager, Galway, Ireland.

Johnson & Johnson is currently seeking a Clinical Research Manager, Galway, Ireland.

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/.

For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.

Our dedication to respect the dignity and diversity of all is embedded in our Credo.

We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences.

That is why we are crafting an inclusive environment where diverse backgrounds, perspectives and experiences are valued and every one of our people feels that they belong and can reach their potential.

No matter who they are.

Diversity, Equity & Inclusion at Johnson & Johnson means "You Belong"!
Duties & responsibilities

Under limited supervision and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:


* Serves as a Clinical Research Manager within the Clinical R&D Department to complete and lead company sponsored clinical trials, ensuring compliance with timelines and study achievements.


* Has oversight of feasibility, selection, set up, conduct and closure of a clinical trial within the allocated countries, in accordance with the ICH-GCP, applicable legislation and Company Standard Operating Procedures;


* Handles and coordinates ordering, tracking, and accountability of investigational products and trial materials;


* Ensures applicable trial registration (e.g.

www.clinicaltrials.gov) from study initiation through posting of results and support publications as needed;


* Is responsible for team's interface and collaboration with key opinion leaders, investigators, IRBs/ECs, Regulatory agencies, contractors/vendors, societies, associations and company personnel.


* May perform monitoring activities including site qualification visits, site initiation visits, interim monitoring visits or close out visits based on study need;


* In EMEA, responsible for Regulatory Affairs related tasks associated with clinical trials and evidence generation.


* Contribute to the development and delivery of appropriate Global EGS (Evidence Generation Strategies)/ EDS (Evidence Dissemination Strategies) to support New Product Development and Life-Cycle...