Senior Clinical Research Specialist

Biosense Webster Inc, part of Johnson & Johnson's MedTech, is recruiting for a Senior Clinical Research Specialist, located in Irvine, CA.

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 https://www.jnj.com/.

Overview

This Senior Clinical Research Specialist will be responsible for supporting one or several clinical trials within the Clinical R&D Department while encouraging strong, positive relationships with co-workers across the organization.

Key Responsibilities

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


* Serve as a Senior Clinical Research Specialist within the Clinical R&D Department to support execution of company sponsored clinical trials, ensuring compliance with timelines and study milestones, for Biosense Webster;


* Oversight/execution 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;


* May serve as the primary contact for clinical trial sites (e.g.

site management);


* Contribute towards development of clinical trial documents (e.g.

study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports), ensure registration on www.clinicaltrials.gov from study initiation through posting of results and support publications as needed;


* Management/oversight of ordering, tracking, and accountability of investigational products and trial materials;


* Collaborate with site personnel, IRBs/ECs, contractors/vendors, and company personnel;


* Supervise the development and execution of Investigator agreements and trial payments;


* Responsible for clinical data review to prepare data for statistical analyses and publications;


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


* May contribute to the development and delivery of appropriate global evidence generation strategies (EGS) and evidence dissemination strategies (EDS) within the assigned projects;


* If applicable, as part of a clinical trial, may provide on-site procedural protocol compliance and data collection support to the center;


* Contribute to the critical assessment of the literature and to the interpretations and disse...