Professional Research Assistant - Data Manager

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

University of Colorado - School of Medicine

Professional Research Assistant

The Division of Hematology, Blood Cancer and BMT Program at the University of Colorado Anschutz Medical Campus has an opening for a full time Clinical Research Data Manager. This position will support our Hematology Clinical Trials Unit (HCTU) and is responsible for the collection, interpretation and documentation of clinical research data.


Clinical Research


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.


  • 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.
  • Ensures complete source documentation is compiled in research records.
  • Assists clinical research coordinator(s) (CRC) in assessing patient eligibility for approved study by:
    • Gathering source documents.
    • Ensuring the current version of consent forms are completed, informed consent process in properly documented and filed.
    • Reviewing medical history to determine eligibility status.
  • Collaborates with clinical research coordinator in obtaining grading levels for toxicities including assessment of clinical significance of all lab and test results and relatedness of adverse reactions to study product according to protocol guidelines.
  • Schedules and tracks submission of prescreening, screening and enrollment logs as required by study sponsor
  • Schedules, coordinates, prepares for and conducts sponsor monitor visits and audits in collaboration with the regulatory team, CRC and other research team members.
  • Meets with monitors to respond to any question of data validity and corrects/revises data as appropriate; answers queries from sponsoring companies.
  • Conducts follow-up of study patients
  • Performs clinical duties as assigned based on appropriate licensure and/or completion of competency documentation.


  • Education: BS or BA


  • 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.
  • Ability to work independently, identify and set priorities, and meet deadlines in a fast-paced work environment.


  • Knowledge of basic human anatomy, physiology and medical terminology
  • Excellent computer skills including proficiency in Microsoft Office products
  • Research experience (oncology experience is a plus)

Salary and Benefits:

Salary is commensurate with skills and experience. The anticipated salary range for this position is $42,000 to $45,000/annually. 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: 4493

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 25, 2016

Closing Date: Ongoing

Posting Contact Name: Lynette Brandon

Posting Contact Email:

Position Number: 00050356


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