Clinical Research Coordinator

Department:
SOM KC Neurology - Neuromuscular

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Neuromuscular Staff
Position Title:
Clinical Research Coordinator
Job Family Group:
Professional Staff
Job Description Summary:
Job Description Summary
The Clinical Research Coordinator works with multidisciplinary teams including patients/ study participants, families, physicians, and administrative staff to coordinate all aspects of clinical trial activities within the Neuromuscular Disease Program. Through careful and well-planed methods, this position ensures that study procedures follow the sponsor's protocol and all applicable regulatory requirements while also ensuring research participants and their families are treated with the utmost respect and concern for their well-being and safety.
Job Description:

Conditions of Employment: Must be available to travel to attend national meetings.

Required Qualifications

Education: Bachelor's degree in basic science or health related field. Related work experience may be substituted for degree on a year-for-year basis.

Work Experience:

• Experience using the Microsoft Office Suite.

• Two (2) years of relevant work experience.

• Experience working with patients, families, physicians, and administrative staff.

Preferred Qualifications

Education/Certifications: SOCRA CCRP certification

Work Experience

• Prior health care and/or research experience.

• Experience with electronic medical records.

• Experience in Neurology and/or Neuromuscular research.

Skills

• Attention to detail

• Time-management skills.

• Interpersonal skills.

• Multitasking skills.

Job Duties  

The Clinical Research Coordinator position is responsible for recruiting, evaluating, and educating patients regarding clinical trials related to neuromuscular disease. This position coordinates all aspects of assigned research studies including recruitment, study visit activities according to protocol, maintenance of the investigator site file, data entry, and other various tasks. 

The Clinical Research Coordinator collaborates with multidisciplinary teams, research, and hospital staff to recruit, screen, educate, and assist in the overall clinical study coordination of clinical research. This position manages assigned clinical research studies by supervising a variety of complex activities involved in the collection, compilation, documentation, and analysis of clinical research data. Monitors study participants’ progress including documenting and reporting adverse events. Participates in periodic quality assurance audits of protocols. 

 

This position will be or become familiar with neuromuscular disease and conducting research according to ICH GCP guidelines. 

The position requires an individual with exceptional communication skills and the ability to multi-task to work collegially with members of the neuromuscular research team to ensure research studies are being conducted according to protocol.  

• Recruits, evaluates, and educates patients regarding clinical trials related to neuromuscular disease.  

• Conducts Informed Consent Interview with participant and caregiver following Neuromuscular Program Standard Operating Procedures (SOP) for obtaining consent from cognitively normal and cognitively impaired individuals. Follows SOP for determination of when use of a Surrogate consent form is necessary, due to extent of cognitive impairment.  

• Documents trial related activities per regulatory requirements in a timely and accurate manner. 

• Coordinates all aspects of study visit activities for patients and families, including scheduling of hospital-based procedures such as MRI and PET, and other procedures to include clinical study visit interviews and assessments, ECG, lab draws, IV infusions, lumbar punctures, and dispensation of study medication. 

• Gathers accurate medical history and concomitant medication information and ensures that medical conditions and medications meet trial specifications. 

• Probes patient/ caregiver for any changes in health throughout clinical trial intervention and monitors for potential adverse events. Obtains complete reports of new symptoms/changes in health conditions and reviews with clinician/principal investigator.   Based on principal investigator’s determination of adverse event (AE) qualification, prepares formal AE report for sponsor and for IRB, when applicable per regulations. If AE meets criteria of Serious Adverse Event (SAE), prepares full FDA MedWatch or sponsor-provided Safety Report and submits to regulatory authorities within 24 hours of learning of event. 

• Assists physician in cerebrospinal fluid (CSF) collection for clinical trials by educating patient / caregiver regarding the lumbar puncture procedure, preparing lumbar puncture supplies, providing supplies to physician during procedure while maintaining sterile field, aliquoting CSF by protocol-specified amounts into separate vials for storage and transport, instructing patient/caregiver in post-lumbar puncture care and expectations, conducting follow –up phone call to determine if any adverse events were experienced.

• Prepares local and central lab requisition forms to ensure proper testing is conducted on CSF, blood, and urine samples.

• Prepares and ships biological specimens to central labs per protocol and regulatory requirements. 

• Conducts interviews with patient and/or caregiver regarding mood, anxiety, neurobehavioral symptoms, and functional abilities. 

• Ensures all study staff completes required training for proper conduct of the trial.

• Ensures investigator’s timely review of lab tests, EMG/ECG/MRI/PET results and communicates clinically relevant information to patient and patient’s primary care doctor as appropriate. 

• Ensures availability of medical records, updated subject records and updated protocols. 

• Updates and maintains regulatory binders.

• Prepares adverse event reports and protocol deviation reports for submission to IRB. 

• Assists the Research Institute regulatory project manager in preparation of IRB submissions, including review of consent forms, nw study and continuing review applications, and protocol amendments.

• Ensures all study data is entered into sponsor-provided and/or internal KU databases per sponsor requirements, typically within 3 business days following data collection. 

• Other duties as assigned.

Required Documents

• Resume/CV

Comprehensive Benefits Package:

Coverage begins on day one for health, dental, and vision insurance and includes health expense accounts with generous employer contributions if the employee participates in a qualifying health plan. Employer-paid life insurance, long-term disability insurance, and various additional voluntary insurance plans are available. Paid time off, including vacation and sick, begins accruing upon hire, plus nine paid holidays. One paid discretionary day is available after six months of employment, and paid time off for bereavement, jury duty, military service, and parental leave is available after 12 months of employment. A retirement program with a generous employer contribution and additional voluntary retirement programs (457 or 403b) are available. https://www.kumc.edu/human-resources/benefits.html

Employee Type:
Regular
Time Type:
Full time
Rate Type:
Salary

Compensation Statement:

The pay range listed for this position is determined by our compensation program using market data and salary benchmarking. A combination of factors is considered in making compensation decisions including, but not limited to, education, experience and training, qualifications relative to the requirements of the position, and funding. At the University of Kansas Medical Center, a reasonable estimate for the starting pay range will be the minimum to midpoint of the posted range, taking into account the combination of factors listed above. 

Pay Range:
$58,000.00 - $86,000.00

Minimum

$58,000.00

Midpoint

$72,000.00

Maximum

$86,000.00