Clinical Research Coordinator

Responsibilities

Provide assistance in the administrative, technical and scientific day-to-day operation of the study to assure project goals and timelines are met, quality data is collected and managed, and to assure participant and/or data confidentiality

Conduct clinical research as outlined in the study protocol. Maintain knowledge of clinical research issues. Follow GCP guidelines. Implement confidentiality and privacy regulations

Evaluate protocols, assist in study selection, correspond/coordinate with the sponsor/CRO and prepare study budgets

Support and assist Research personnel in the operation of equipment used in clinical trials

Support the development of Quality Assurance procedures, and assist with the monitoring of data collection and data transfers. Assist with the preparation of annual IRB reviews

Support the Project Director, Clinic Coordinator, or PI in the administration of the grant/contract per federal rules and regulations and/or specific grant/contract language. Understand the operational budget and sub-contracts; track documentation and authorization of payment of study related bills. Provide assistance in the preparation of project reports for PI review and approval

Recruit study participants to a broad range of studies using specific study protocols to contact, screen, and determine eligibility and schedule appointments with study participants

Collect, edit and record/enter study data via interview, structured interview, questionnaire, medical record review, and basic clinical measurements for complex study protocols, and perform technical duties as assigned

Support orientation and structured intervention sessions in accordance with technical training and certification(s)

Assist with case management activities to support the work of the project(s)

Support the process of summarizing and sharing project information with other sites. Support the Project Director, Clinic Coordinator, and/or PI in the maintaining regular contact with other Project Administrators in order to share information and ideas. Assist with the tracking of papers in process for projects, with planning for project papers and posters to be presented at national and international conferences

Adheres to all safety policies and procedures in performing job duties and responsibilities while supporting a culture of high quality and great customer service

Perform other duties in support of clinical trials services as assigned

Preferred

Undergraduate degree in a related field preferred

Experience in health research or research data collection is preferred

Familiarity with classification of disease processes is preferred

Knowledge of basic research ethics and principles is preferred

Benefits

Full Benefits Package - Medical, Vision, Dental and Life Insurance

401k + Employer Matching

Paid Time Off (PTO) and Paid Holidays

Paid Maternity Leave

Employee Discounts

We do pay mileage reimbursement!

A growing family of independent primary eyecare practices and a portfolio company of FFL Partners.

St Louis, Missouri, USA

http://eyecare-partners.com

Late Stage

Total Funding

unknown

2019-12-16

Acquired

Leadership Team

Chris Throckmorton

Chief Executive Officer

Kirby Cole

Vice President, Talent Acquisition and Provider Relations

Recent News

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Qualifications

Demonstrated interpersonal, communication and interviewing skills with people of all ages

Organized, detail oriented, self-directed and dependable

Able to prioritize work, solve problems and work independently

Able to function in a team environment and use negotiation skills

Favorable result on background check required

Must be able to provide proof of identity and right to work in the United States

High school diploma or general education degree (GED) required

At least one (1) year of experience collecting information using one of the following methods: Telephone/face-to-face interviews, Working with patients and study participants in a clinical situation (proficiency in refracting patients needed)

One year of experience collecting or processing data for research or Quality Assurance purposes

Working knowledge of medical terminology, anatomy, and disease processes; medical record organization and interpretation

Proficient in Microsoft Excel, Word, PowerPoint, Outlook

Basic knowledge of computer functions

Able to use computers and software programs for complex tracking of participant tasks

This role requires a variety of physical activities to effectively perform essential job functions. The position involves frequent walking (75%), sitting (50%), and standing (50%), with regular bending, stooping, and reaching (25–50%). Employees must be able to lift, carry, push, and pull items up to 25 lbs. Strong fine motor skills and full use of hands are essential, as the role demands constant grasping, writing/typing, and use of technology. Visual and auditory acuity—including color, depth, peripheral vision, and the ability to adjust focus—is required 100% of the time. Occasional driving or climbing may also be necessary

Undergraduate degree in a related field preferred

Experience in health research or research data collection is preferred

Familiarity with classification of disease processes is preferred

Knowledge of basic research ethics and principles is preferred

At least one (1) year of experience collecting information using one of the following methods: Telephone/face-to-face interviews, Working with patients and study participants in a clinical situation (proficiency in refracting patients needed).

One year of experience collecting or processing data for research or Quality Assurance purposes.

Required skills

Clinical research, Clinical Practice (GCP) guidelines, Study protocol evaluation, Quality Assurance procedures, IRB review preparation, Medical terminology, Anatomy, Disease process classification, Data collection methods, Microsoft Excel, Microsoft Word, Microsoft PowerPoint, Microsoft Outlook

Preferred skills

Undergraduate degree in a related field preferred

Experience

1+ years