Position Summary:

　　To facilitate and coordinate clinical trials using good clinical practice under the direction of the Investigators and Director. A CRC is responsible to ensure compliance with protocols and overall objectives, oversee subject recruitment, subject care, report adverse events and maintain required records of study activity. Works in a collaborative and cooperative relationship with other members of the research center’s team as well as study CROs and sponsors.

　　Minimum Qualifications:

　　Associates or Bachelor’s Degree

　　American Heart Association BLS

　　Proficient with Microsoft Windows and Word

　　Public relations skills

　　Preferred: Certified Clinical Research Coordinator recertification every 2 yrs.

　　Preferred: Phlebotomy Certification

　　Preferred: Previous Clinical Research Coordinator (CRC) experience

　　Preferred: Experience with Excel and Powerpoint.

　　Essential Job Functions:

　　Site Initiation Visits

　　Travel to Investigator Meetings

　　Investigator Meeting Webinars and Recruitment Webinars

　　Independent protocol review

　　Electronic Data Capture

　　eDiaries

　　Good Clinical Practice

　　Interactive Web Response Systems

　　Safety-Pak lab shipments

　　Laboratory procedures for collecting and shipping

　　B. RECRUITMENT:

　　Checking online recruitment sites

　　Following up with referrals

　　Mass emails, mailing letters (labels, stamping, stuffing envelopes)

　　Taking patient calls from advertisements

　　Reveal and recruitment log updates

　　Scheduling screening visits

　　Walk-ins

　　Supply ordering (medical and office)

　　Regulatory (filing)

　　Answering phones, setting up voicemails

　　Temperature logs

　　Mail

　　Faxing/receiving medical records request

　　Scheduling patients

　　EDC entry

　　Staff meetings/minutes

　　Faxing patient logs/patient log updates

　　Walk-ins (patients, FedEx)

　　IT help/facility work orders

　　Informed consent process

　　Patient care/patient training/patient compliance

　　Procedures (ECG, labs, vitals, height/weight, spirometry)

　　eDiary training

　　Study drug training, dispensing, collecting and completion of accountability logs

　　Study drug and eDiary compliance

　　Adverse events

　　Scheduling visits

　　Processing and shipping lab samples

　　Documentation/EDC entry

　　Following up with study drug and diary compliance

　　Visit reminders

　　Medical record review/reconciliation

　　Adverse event follow-up

　　Source creation and editing

　　Queries

　　Other duties as assigned

　　Knowledge, Skills and Abilities

　　Demonstrates sound judgement, patience, and maintains a professional demeanor at all times

　　Ability to work in a busy and stressful environment

　　Strong interpersonal, verbal and written communication skills

　　Exercises tact, discretion, sensitivity and maintains confidentiality

　　Computer applications, MS Office, EMR, internet applications and standard office equipment

　　Detail oriented, organizational skills and the ability to prioritize

　　Strong emotional intelligence, interpersonal and teamwork skills

　　The above statements are intended to describe the general nature and level of work being performed by people assigned to the job classification. They are not to be construed as a contract of any type nor an exhaustive list of all job duties performed by individuals so classified.

　　77387225 Clinical Research Studies

　　Working at Bozeman Health is more than just a job--it's a commitment to caring for the communities of Southwest Montana by being their partner in health and wellness, compassionately delivering the best care for each person, every time. In every role, our employees are inspired by their ability to care for our community and our Culture of Excellence guides each employee to be a high performer, engage in transparent and timely communication, demonstrate dynamic learning and teaching, excel through change, express gratitude and experience joy.