What are the responsibilities and job description for the Clinical Research Coordinator position at Hematology Oncology Associates Of Central New York?
Job Type
Full-time
Description
Hematology Oncology Associates of CNY (HOACNY), voted one of Central New York's Best Places to Work, is looking for a full time Clinical Research Coordinator to join our professional team. HOACNY provides cancer care services, Monday through Friday, day hours at three convenient locations in East Syracuse, Syracuse and Auburn. If you are a highly motivated, team oriented individual looking to make a difference in your career, please apply now.
Starting salary (based on experience) stipends / bonuses. Generous benefits package including medical, dental, life, std, ltd, 401k / pension, tuition reimbursement, etc. Convenient free parking.
A Clinical Research Coordinator is responsible for all aspects of clinical treatment trials in accordance with HOA policies and procedures, federal and international regulations regarding the conduct of research involving human subjects, including but not limited to : study evaluation and initiation, subject screening and recruitment, timely and accurate data collection and submission.
Responsible for protocol evaluation and feasibility, including budget evaluation and trial preparation involving the planning, development and evaluation of patient information and patient recruitment materials.
Responsible for preparation of required forms and materials for initial and continuing Institutional Review Board (IRB) review, tracks and completes all regulatory-related processes, including reporting of adverse events on assigned studies.
Hematology Oncology Associates of CNY is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status. HOA is also committed to compliance with all fair employment practices regarding citizenship and immigration status.
Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa.
Requirements
Strong verbal and written communication skills
Strong interpersonal skills; enjoys collaboration; works well with patients and colleagues
Ability to work in teams
Ability to work autonomously
Strong critical thinking and problem solving skills
Strong organizational skills
Attention to detail
Ability to set priorities and reprioritize quickly
Advanced computer skills / high comfort level with technology / electronic medical records
Education : College Degree required
Experience : Two years experience in a clinical research environment.
Two years medical experience with medical terminology familiarity
Oncology experience preferred
Certificate / License : Certified Clinical Research Associate (CCRA) or Certified Clinical Research Coordinator (CCRC) desirable at time of hire; must obtain within three years of employment
ALTERNATIVE TO MINIMUM QUALIFICATIONS : Additional appropriate education or work experience may be substituted for clinical research experience.
Salary Description
22.00
Salary : $22
