Professional Research Assistant - Tissue Bank Coordinator/Data Manager

Location
Aurora, CO
Posted
Feb 21, 2017
Institution Type
Four-Year Institution




University of Colorado - School of Medicine

Professional Research Assistant

POSITION SUMMARY
The Division of Hematology, Blood Cancer and BMT Program at the University of Colorado Anschutz Medical Campus has an opening for a full time Tissue Bank Coordinator/Data Manager. This position will assist in the implementation and coordination of clinical trials.

PROFESSIONAL FIELD

Medical/Clinical Research

ABOUT THE PROGRAM

The faculty of the Division of Hematology are responsible for teaching, clinical care and research in all aspects of Hematologic Disorders. Our division has physicians and advanced practice providers who are devoted primarily to clinical care and clinical research, physician scientists who divide their time between the lab and the clinic and scientists who spend their time focused primarily on laboratory research. Because we take such an integrated approach to the diagnosis, treatment and curing of blood disorders we are able to move treatments from the bench to the bedside in a significantly more timely fashion.

Our patients have access to clinical teams assembled specifically for each type of cancer - and all of these specialists are seen at one location, in one visit. Our medical teams meet regularly and work together to evaluate all cases, plan and deliver treatment, manage side effects and provide support for the entire treatment arc, including helping our patients stay healthy and tackle physical and emotional challenges after treatment.

The Division of Hematology also has the responsibility to promote clinical trials research efforts across the spectrum of hematology, and is committed to investigations involving non-malignant hematological disorders, as well as across all age spectrums, including pediatric hematology.

EXAMPLES OF WORK PERFORMED

  • Recruits and interviews prospective subjects for Heme/BMT cancer tissue bank clinical studies. Familiarizes potential subjects with the details of the study through phone contacts and personal interviews.
  • Ensures accurate data entry of tissue bank patient data and other clinical trial data as assigned.
  • Obtains medical history and current medications, reviews protocol inclusion/exclusion criteria, and confirms eligibility of subject. Ensures that the informed consent process has occurred, is properly documented and filed as required.
  • Abstracts and records all patient data essential to the study onto required Case Report Forms (CRFs) and into the Clinical Trials database, as needed, in an accurate and timely fashion. Maintains patient clinical research files.
  • Reports adverse events and serious events to appropriate parties; e.g. Principal Investigator, Study Sponsor, FDA, PQASC, Regulatory Affairs Coordinator.
  • Serves as a contact person for ongoing clinical research studies. Schedules monitoring visits and meets with representatives from sponsoring pharmaceutical firms or in-house staff for initial orientation to studies and for review of study records.
  • May be called upon to perform the following specific tests and procedures: c) phlebotomy (direct venipuncture) d) specimen processing and shipping



Qualifications

MINIMUM REQUIREMENTS

  • Education: BS or BA


KNOWLEDGE, SKILLS & ABILITIES

  • Excellent interpersonal communication, organizational skills, and ability to problem solve and multi-task.
  • Good command of the English language, both written and verbal.
  • Excellent attention to detail and ability to interpret and master complex protocol information.

PREFERRED QUALIFICATIONS

  • 1 year experience in a clinical setting (oncology data management experience is a plus).
  • Knowledge of basic human anatomy, physiology, medical terminology.
  • Excellent computer skills including proficiency in Microsoft Office products.


Salary and Benefits

The anticipated salary range for this position is $42,000 to $46,500/annually and is commensurate how with skills and experience. The University of Colorado offers a full benefits package. Information on University benefits programs, including eligibility, is located at Employee Services.

The University of Colorado Denver is dedicated to ensuring a safe and secure environment for our faculty, staff, students and visitors. To assist in achieving that goal, we conduct background investigations for all prospective employees.

The University of Colorado strongly supports the principle of diversity. We encourage applications from women, ethnic minorities, persons with disabilities and all veterans. The University of Colorado is committed to diversity and equality in education and employment.

The Immigration Reform and Control Act requires that verification of employment eligibility be documented for all new employees by the end of the third day of work. Alternative formats of this ad are available upon request for persons with disabilities.



Application Materials Required:Cover Letter, Resume/CV, List of References

Application Materials Instructions:

Applications are accepted electronically at CU Careers, refer to requisition ID: 4512

When applying, applicants must include:
  1. A letter of application which specifically addresses the job requirements and outlines qualifications
  2. A current Resume/CV
  3. The names, addresses, daytime telephone numbers and e-mail addresses for three professional references, either attached to your resume/CV or uploaded as a separate document
Please be advised that the University does check references as part of the employment process.

Please do not submit any of your application material (via email) to the job posting contact.



Job Category: Faculty

Primary Location: Aurora

Department: H0001 -- Anschutz Medical Campus - 20164 - SOM-MED-BoneMarrow Transplant

Schedule: Full-time

Posting Date: Mar 29, 2016

Closing Date: Ongoing

Posting Contact Name: Lynette Brandon

Posting Contact Email: lynette.brandon@ucdenver.edu

Position Number: 00708768

PI96904317