Clinical Research Coordinator II (Frederick/Germantown)

Responsibilities

Screens potential patients for protocol eligibility. Presents trial concepts and details to the patients, participates in the informed consent process, and enrolls patients on clinical trials

Coordinates patient care in compliance with protocol requirements. May disburse investigational drug. Maintains investigational drug accountability. Oversees the preparation of orders by physicians to assure that protocol compliance is maintained. Packages and ships lab specimens to central vendors where applicable. Required to complete Hazmat and/or IATA training

In collaboration with the physician, reviews patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to study drug and thoroughly documents all findings and participates in data collection of all subjects

Responsible for preparing study-related documentation such as protocol worksheets, adverse event reports, institutional review board documents, and annual continuing review reports

Maintains regulatory documents in accordance with USOR SOP and applicable regulations. May participate in scheduling monitoring and auditing visits, as well as interact with the monitors/auditors while onsite. May collaborate with Research Site Leader in the study selection process

Participates in required training and education programs. May be responsible for education of clinic staff regarding clinical research. Collaborates with staff in the development of action plans and performance improvement opportunities with staff to improve quality

May be responsible for compiling and reporting protocol activity, accrual trends, data entry compliance, and research financial information to practice administration and physicians. May be responsible for reviewing protocol specific billing guides and submitting billing information to appropriate personnel

Preferred

Bachelor's degree preferred

SoCRA or ACRP certification preferred

Experience working with physicians preferred

Experience working in clinical research is preferred

Benefits

A dynamic and supportive environment where you can grow and thrive.

Every day, The US Oncology Network helps approximately 3,300 providers deliver value-based, integrated care for patients—close to home.

The Woodlands, Texas, USA

http://www.usoncology.com/

Late Stage

Total Funding

unknown

2010-12-30

Acquired

Recent News

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Qualifications

Associate's degree in a clinical or scientific related discipline required

Minimum three years of experience in a clinical or scientific related discipline required

Experience in Microsoft Office

Must have excellent communication skills

Excellent organizational skills

Strong ability to multi-task

Excellent time management skills

Must have strong interpersonal skills to be able to interact with multiple people on many different levels

Must have a high level of attention to detail

Must be able to work in a fast-paced environment

The successful candidate will demonstrate extensive experience in patient-facing roles, maintaining a professional and empathetic demeanor while delivering high-quality care

This position requires a self-motivated individual who can work independently and manage priorities effectively in a fast-paced environment

This is a full-time, on-site role with a schedule of Monday through Friday

Large percent of time performing computer based work is required

Requires standing and walking for extensive periods of time. Occasionally lifts and carries items weighing up to 40 lbs. Requires corrected vision and hearing to normal range

Bachelor's degree preferred

SoCRA or ACRP certification preferred

Experience working with physicians preferred

Experience working in clinical research is preferred

Minimum three years of experience in a clinical or scientific related discipline required,

Required skills

Clinical Research, Oncology, Microsoft Office, Basic Clinical Assessments, SoCRA or ACRP Certification

Preferred skills

Bachelor's degree preferred, SoCRA or ACRP certification preferred, Experience working with physicians preferred, Experience working in clinical research is preferred

Experience

3+ years