What are the responsibilities and job description for the Clinical Research Coordinator II - Contract position at ARIZONA ARTHRITIS & RHEUMATOLOGY ASSOCIATES?
Job Description
Job Description
Description :
Job Title Clinical Research Coordinator II
Reporting to Regional Research Manager
Location Willow Grove, PA
Permanent Full Time (1099) Contractor Position
- Provides study information and obtains relevant information as required by the protocol, from patients who are participating in, or interested in clinical studies.
- Assists in the recruitment and screening of volunteers, schedules patient visits in EMR, provides information to potential subjects and those participating in clinical trials and obtains relevant medical history by telephone and in person. Collects relevant medical records when needed.
- The CRC is responsible for meeting recruitment goals for each study. The methodology of recruitment will include, but is not limited to daily chart review, advertising when funds are available, referrals from rheumatologists and other staff and may include attending health fairs and community outreach.
- Reviews and administers the informed consent form to subjects; allowing them time to read and ask questions. Provides progress notes in EMR and source documents to describe procedures at each visit.
- Plans, prepares and performs tasks required by protocol, which may include, but not limited to the following :
- Obtaining patient medical history and medication lists
- Phlebotomy and basic laboratory tests
- Patient education and training
- Administer Questionnaires
- Vital signs
- Assist with Joint counts and other assessments
- Data Entry
- Study drug administration, including injections
- Triages adverse events and communicates with the research physician regarding the occurrence of adverse and serious adverse events. Follow-up with the subject and collateral informants as needed.
- Provides educational information to subjects. Serves as a resource and support person for subjects and families by being a consistent person they can contact within the clinical research program.
- Ensures uniform implementation of protocols by completing required documentation in a consistent, accurate and timely manner. Assists in preparing appropriate Institutional Review Board (IRB) forms, informed consents, correspondence with sponsor, etc., in an accurate and timely manner. May participate in the annual IRB approval and update process.
- Serves as a liaison to all physicians and AARA employees.
- Ensures that primary referring physicians receive timely progress notes on the patient’s diagnosis and treatment.
- May assume primary responsibility in the implementation and management of new clinical trials in a knowledgeable and collaborative manner. Performs all functions according to established policies (SOPS), procedures, regulatory and accreditation requirements, as well as applicable professional standards.
- Provides all AARR research subjects with an excellent service experience by consistently demonstrating professional decorum
Assignment and Review of Work
All new AARA employees will agree initial objectives to be assessed on completion of their 90-day initial review period. Thereafter, all employees will enter the annual appraisal cycle under the AARA Talent, Performance and Career Management Policy where annual appraisals will be conducted by their Line Manager and CRO. Further information on the appraisal cycle calendar is available from the HR Manager and from the Talent, Performance and Career Management Policy on the AARA Intranet.
Communication and Relationships
The postholder must have strong interpersonal and relational talents. Success in this role involves building and maintaining relationships with internal and external stakeholders
Demands of the Job
Role requires frequent light physical effort. The role requires a combination of sitting, standing and walking.
Role requires frequent, moderate mental effort. The role requires a consistent high level of concentration, attention to detail and organization.
Role requires frequent, light emotional exposure to distressing diagnoses. Occasional direct moderate emotional exposure to patients or relatives who may be ill, upset, distressed or angry.
Role requires frequent exposure to hazardous materials and contact with contained bodily fluids.
Requirements :
11. Knowledge, Skill, Training and Experience to do the Job
Essential