DOCS Sr. Site Manager *** COUNTRY*** Home based / office based in Des Moines, Iowa
Sr. Site Manager * COUNTRY* Home based / office based
Ref #: 31495
Employment type: Permanent - Full-Time
Location: United States
ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations.
With our patients at the center of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.
Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.
ICON is searching for Sr. Site Manager Candidates in XXX. The position is home-based for Sr. SM's with 3-5 years of on-site monitoring experience in XXX clinical trials.
The Clinical Research Associate monitors activities at clinical study sites to assure adherence to Good Clinical Practices (GCPs), SOPs and study protocols. Reviews regulatory documents as required and prepares site visit reports. Responsible for multiple projects and must work both independently and in a team environment. May participate in the study development, start-up and close-out process including reviewing protocols, preparing Informed Consent forms, developing key study documents, organizing and presenting at investigator meetings, working with management on monitoring strategy and performing other tasks as assigned. Continues professional training to maintain awareness of developments in the field of clinical research.
• Prefer BS/BA or RN
• At least 3-5 years site monitoring experience
• Ability to provide mentoring to fellow team members
• Customer service orientation
• Sound knowledge of medical terminology, clinical monitoring process, FDA regulations and ICH guidelines
• Experience monitoring XXX clinical trials at CRO or Pharmaceutical Company, with ability to analyze and articulate protocol issues with medical staff.
• Ability to perform travel in XXX area for site visits
• Excellent verbal and written communications skills
• Excellent interpersonal and organizational skills and attention to detail.
• Computer literacy, proficiency in MS Office
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.
DOCS is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment.
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