Clinical Research Coordinator, On-site, Omaha, NE
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Job Location:
Monthly Salary:
Posted on:
11 hours ago
Vacancies:
1 Vacancy
Job Summary
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 can-do 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.
Key Responsibilities:
- Coordinates advanced clinical research projects as the primary CRC on at least 4 studies of medium to high complexity as well as back-up CRC on other studies when needed
- Assures that the integrity and quality of clinical research trials is maintained
- Develops and implements patient recruitment strategies; actively recruits to ensure enrollment targets are achieved
- Oversees the work of research assistants and trains junior staff as appropriate
- Works effectively with multidisciplinary ancillary and inter-professional research teams
- Functions independently and is able to identify situations where additional support is necessary
- Completes all protocol related training
- Performs patient/research participant scheduling
- Collects patient/research participant medical history
- Collects and maintains source documentation
- Manages inventory and administers test articles/investigational product to 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
- Obtains informed consent of research subjects
- Supports the safety of research subjects report adverse events.
- Coordinates protocol related research procedures study visits and follow-up
- Facilitates site qualification study initiation and monitoring visits and study close-out activities
- Ensures proper collection processing and shipping of laboratory specimens
- May be asked to perform special project responsibilities and travel to other locations when needs arise
- Complies with Avacare Clinic and Sponsor policies standard operating procedures (SOPs) and guidelines
- Performs other duties as assigned
Required Knowledge Skills and Abilities:
- Must demonstrate the ability to fulfill responsibilities of CRC Level I
- Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines
- Knowledge and experience of site operations and the drug development process
- Excellent written and verbal communication skills must be comfortable and effective in communicating with potential study participants from a diverse population Interpersonal skills - open to others ideas and willing to learn new things; respond well to questions and challenges
- Process improvement support ideas and theories on process improvement for efficiency and effectiveness
- 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. is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements misrepresentations or material omissions during the recruitment process will result in immediate disqualification of your application or termination of employment if discovered later in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role when annualized is $36600.00 - $91300.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge skills education and experience; location; and/or schedule (full or part-time). 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
Key Skills
- Experience Working With Students
- Google Docs
- Organizational skills
- Classroom Experience
- Data Collection
- Materials Handling
- Workers' Compensation Law
- OSHA
- Special Operations
- Team Management
- Experience with Children
- Supervising Experience
About Company
IQVIA is the Human Data Science Company™. We are inspired by the industry we serve and provide solutions that enable life sciences companies to innovate with confidence, maximize opportunities and ultimately drive human health outcomes forward. Our approach is Human Data Science – a d ... View more
