Ref #: 30600

Employment type: Permanent - Full-Time

Location: US - Remote

Posted: 27-Sep-2021

Description

If you are seeking a career where you can truly make a difference in the lives of others, working closely together with the top minds in the pharmaceutical Industry, then here is your chance. We are looking for a CRA or Sr CRA with a Lab background and two years of on-site monitoring experience.

The Clinical Research Associate will be responsible for designing, planning, coordinating, and conducting all activities involved in initiating, monitoring, and completing clinical research studies.

Responsibilities include but are not limited to:
•Ensuring studies are conducted and documented in accordance with the study protocol, standard operating procedures, good clinical practices and other applicable regulatory requirements
•Validating product performance claims
•Supplying data for critical Regulatory submissions
•Defining the functional and clinical utility of investigational products, and obtaining opinions and input regarding investigational products from laboratories or customers, who may be considered key opinion leaders
•Performing or coordinating aspects of clinical studies including site selection, study initiation, site monitoring, and study closeout
•Maintaining communication with study investigators to ensure studies are completed in a timely fashion and ensuring that study objectives are met
•Interfacing with other cross functional staff to support post launch activities
•Reviewing cases with investigators to resolve discrepancies

Requirements:
•Bachelor's degree in science or relevant field
•2 years of on-site monitoring experience
•Lab background preferred

DOCS is the FSP division of ICON Clinical Research. We provide global strategic resourcing and FSP services to the biopharmaceutical and medical device industries. Founded in 1997, DOCS has grown to become the premier resourcing provider for the clinical development industry.

DOCS is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment.

Benefits of Working in ICON:
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.

At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.


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