MD Anderson Cancer Center Coord, Clinical Studies - Lymphoma/Myeloma in Houston, Texas

Coord, Clinical Studies - Lymphoma/Myeloma

Location: United States, Texas, Houston, Houston (TX Med Ctr) at

Research at

Cancer Medicine 135100

Requisition #: 117160

From caring for patients to conducting clinical and translational research, the Lymphoma and Myeloma department is one of the largest multidisciplinary programs treating these cancers of the blood in the U.S.

The Clinical Studies Coordinator provides administrative and patient care services for the coordination of clinical trials.

The salary range is: min-$49,600, mid-$62,000 and max-$74,400.

Assists the Investigator

Assists the investigator in the overall conduct of clinical trials as assigned. Participates in the departmental protocol review and submission process and actively participates in protocol meetings such as investigators and initiation meetings as required. Works with Research Nurse and Research Data Coordinator as assigned to assist with protocol initiation through study close out and data review for publication. Assistance with serious adverse event reporting and follow up as needed and assists with subject screening to determine eligibility for study participation.

Manages Protocols

Manages protocols at appropriate intervals. Ensures conduct of assigned studies is in accordance with Good clinical practice, federal regulations and institutional policies. Develops and maintains systems for the coding, editing, and computer entry of data for assigned research studies focusing on continuous patient follow-up.

Report Management

Designs and maintains management reports on the databases for various research studies. Assist the investigator in data file preparation and participates in data review meetings as required by the department. Prepares specific protocol reports and analysis to aid decisions regarding therapeutic efficacy and to assist in manuscript preparation and grant submissions. Ensures prospective data collection into the departmental database and/or study CRF. Is an active participant in the continuing review process. Leads the preparation for protocol monitoring, audits and follow up along with coordinators of research data. Leads all data management efforts for clinical trials as assigned by team and as needed based on departmental priorities and disease team priorities.


Required: Bachelor's degree in Public Health, Healthcare Administration or related scientific field.


Required: Three years experience in area of research study or direct patient care obtained from nursing, data gathering or other related experience. Additional years of related experience and/or education may be substituted on a one to one basis.

It is the policy of The University of Texas MD Anderson Cancer Center to provide equal employment opportunity without regard to race, color, religion, age, national origin, sex, gender, sexual orientation, gender identity/expression, disability, protected veteran status, genetic information, or any other basis protected by institutional policy or by federal, state or local laws unless such distinction is required by law.