drjobs Clinical Research Coordinator On-Site Salt Lake City Utah

Clinical Research Coordinator On-Site Salt Lake City Utah

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1 Vacancy
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Job Location drjobs

Salt Lake, UT - USA

Monthly Salary drjobs

$ 43500 - 72500

Vacancy

1 Vacancy

Job Description

This is a fully onsite position at our Salt Lake City Utah location

Overview:

This individual will play a key role in assisting in the conduct of clinical trial activities in accordance with all applicable regulations governing the conduct of clinical trials. The primary skills include logical thinking ability to prioritize cando attitude the ability to adapt quickly to changing business conditions strong interpersonal and team building skills. The employee working closely with study team members will achieve study objectives and corporate goals.

Essential Functions

  • Ability to coordinate as primary CRC on at least 13 studies of low to medium complexity with oversight by a manager or higherlevel CRC.

  • May assist as backup CRC on other studies

  • Develops and implements patient recruitment strategies; actively recruits to ensure enrollment targets are achieved

  • Obtains informed consent of research subjects

  • Develops strong working relationships and maintain effective communication with study team members

  • Completes all protocol related training

  • Performs patient/research participant scheduling

  • Collects patient/research participant history

  • Collects and maintains source documentation

  • Manages inventory and administers test articles/investigational productto participants

  • Performs data entry and query resolution

  • Supports the collection and review of required essential study documents and reports. Order supportive study supplies (e.g. contracts IXRS lab kits nonclinical supply materials imaging and laboratory handling manuals etc.

  • Adheres to an IRB approved protocol

  • Supports the safety of research subjects report adverse events

  • Coordinates protocol related research procedures study visits and followup

  • Facilitates prestudy site qualification study initiation monitoring visits and study close out activities

  • Collects processes and ships laboratory specimens

  • May be asked to perform special project responsibilities and travel to other clinic locations within the area when needs arise

  • Complies with Avacare and Sponsor policies standard operating procedures (SOPs) and guidelines

  • Performs other duties as assigned

Qualifications

  • Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines

  • Clinical Research Coordinator experience within a similar setting

  • Clinical skills experience including obtaining vitals phlebotomy EKG etc.

  • Knowledge and experienceof site operations and the drug development process

  • Effective communication

  • Computer proficiency in use of Microsoft Word Excel

IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity national origin disability status as a protected veteran or any other status protected by applicable law. potential base pay range for this role when annualized is $43500.00 $72500.00. The actual base pay offered may vary based on a number of factors including jobrelated qualifications such as knowledge skills education and experience; location; and/or schedule (full or parttime). Dependent on the position offered incentive plans bonuses and/or other forms of compensation may be offered in addition to a range of health and welfare and/or other benefits.


Required Experience:

IC

Employment Type

Full-Time

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