Company

The Cancer & Hematology CentersSee more

addressAddressGrand Rapids, MI
type Form of workFull-Time
CategoryEducation/Training

Job description

Our Mission: At The Cancer & Hematology Centers we are dedicated to help, healing and hope for cancer patients and their families.
We provide our patients with advanced treatments, innovative research and, above all else, compassionate care. Our patients receive the most comprehensive, contemporary cancer care balanced with the compassion of a dedicated nursing and support staff. Treating cancer requires a team of committed and caring health care professionals working together to understand and address your needs. In addition to caring physicians, we have a full range of support staff available to assist you and your family, such as oncology-certified nurses, social workers, experienced lab and pharmacy personnel and a psychologist. Our focus is not just on healing but also on helping and offering hope. We know that being diagnosed with cancer is a life-changing event, and it takes a lot of adjustment to accept the emotional and physical realities of this disease. Our staff understands what you're going through and can offer compassion and resources to help. To us, it's important that healing isn't just centered on your disease site. Our cutting-edge cancer care is available close to home. Our medical staff have close ties to prominent hospitals and ongoing cancer research, and we bring those breakthrough advances to our regional centers to progress the level of care that is offered right here at home.
Why Join Us? We are looking for talented and high-motivated individuals who demonstrate a natural desire to support the meaningful work of community oncologists and the patients we serve.
Job Description:
General Summary:
Is assigned multiple protocols at any time for which they will oversee the aspects of assigned protocols with planning and coordinating patient participation in the trial.
Is responsible for implementation as well as completion of protocol specific requirements. Will provide accurate, up to date information to all team members involved with any aspect of carrying out protocol specific requirements.
Will assist in the maintenance of all study related Case Report Forms, whether paper or electronic as well as know status of completion. Will understand the ethical issues involved in human subjects research, adhering to the Federal Regulations governing research.
Communicates on a regular basis with Study Sponsor's, CRO's, staff, etc. regarding questions, concerns, as well as status of the protocol. Will have regular communication with each CRA involved with assigned protocols.
Job Requirements:
Education: Bachelor degree or equivalent.
Experience: Prior experience in clinical trials coordination.
Other: Knowledge and training in general office administration skills, including computer applications, filing systems, etc. Demonstrated ability to accurately and efficiently complete assignments in Clinical Investigations and demonstrated capability to perform the data review and CRF completion in its entirety with minimal direction.
Preferred Knowledge/Skills/Abilities/Education/Experience:
Bachelor degree in life sciences. Additional demonstration of clinical research knowledge as evidenced by the use of either CCRP or CCRC credentials is highly desirable. Familiarity with medical terminology desirable.
Excellent written and verbal communication skills. Ability to review detailed data and make prompt judgments based on that data. Ability to work efficiently under tight deadlines, interruptions and high work volume. Professional appearance. Able to multi-task efficiently.
Primary Duties and Responsibilities (Essential Functions):

  • Will monitor the overall day-to-day conduct of assigned studies in accordance with the specified protocol requirements, Standard Operating Procedures, and Good Clinical Practice to ensure integrity regarding all aspects of the study.
  • Reviews forms created or revised for assigned trials to assure protocol compliance
  • Maintains files using standardized study document labeling and filing procedures
  • Implements initial protocol and amendments, training staff who will be involved in patient treatment and management
  • Maintains an up to date contact list
  • Assists with patient screening and determination of eligibility
  • Facilitates the informed consent process ensuring that consent is appropriately completed.
  • Prepares and manages source documents according to standard operating procedures
  • Will recognize deviations to the protocol and will work with management and staff to address corrective actions to prevent deviations
  • Will assist CRA with case report form completion and query resolution.
  • Will work with the Principal Investigator to complete and submit Serious Adverse Event reports.
  • Is responsible for all protocol specific closeout related activities in conjunction with the CRA.
  • Will provide documentation for all deviations whether related to the protocol or a SOP.
  • Will ensure that all team members involved understand and adhere to assigned protocols.
  • Will also be responsible for any other duties to which they are assigned.

Function as a team member by expanding his/her responsibilities as directed by management to facilitate optimal workflow within the cancer center.
Communicates and interacts with peers and other departments in a manner that is viewed as having a positive effect on patient services and CHCWM staff morale. Interacts effectively with patients/family members and demonstrates sensitivity in regards to cultural diversity, age specific needs and confidentiality.
These functions are intended to describe the general nature, level and requirements of work being performed within this position. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of personnel so classified. The listed duties may be changed at the discretion of management.
This employee has access to medical records daily. The parts of the medical record s/he needs to references to perform his/her job are as follows: Lab Information System, Pharmacy Information System, Entire Chart/Electronic Medical Record (EMR), Electronic Billing System (EBS).
Refer code: 7771446. The Cancer & Hematology Centers - The previous day - 2024-01-08 13:27

The Cancer & Hematology Centers

Grand Rapids, MI
Popular Study Coordinator jobs in top cities

Share jobs with friends

Related jobs

Start Midwest Research Study Coordinator

Clinical Study Coordinator - 40 hrs/wk - Days - Detroit

Henry Ford Health

Detroit, MI

14 hours ago - seen

Research Study Coordinator

Henry Ford Health

Detroit, MI

2 weeks ago - seen

Clinical Study Coordinator - 40 Hours - Days

Henry Ford Health

Detroit, MI

2 months ago - seen

Study Abroad Program Coordinator

Michigan State University

$37.7K - $47.8K a year

East Lansing, MI

3 months ago - seen

Study Coordinator (START MIDWEST)

Cancer & Hematology Centers of Western Michigan

Grand Rapids, MI

6 months ago - seen