Research Coordinator - Oncology Clinical Trials Crystal Lake

American Addiction Centers•Crystal Lake, IL

14d•$31 - $46

About The Position

Coordinates the conduct of oncology clinical trials with an emphasis on the screening, enrolling, and monitoring of cancer patients at AMG Crystal Lake Oncology/Good Shepherd. Provides guidance to physicians, clinical staff and research team members. Coordinates assigned research studies in collaboration with other team members, including but not limited to; study start-up, recruitment, screening, and enrollment of research subjects, development of mechanisms to maximize subject adherence to the research protocol, maintain source documentation, data collection (i.e. development, completion and submission of case report forms (EDC), study drug/device accountability, monitoring of subjects, AE/SAE reporting, study close out, and other elements of study coordination.

Requirements

Bachelor's Degree in Biology, or Bachelor's Degree in Health Science, or Bachelor's Degree (or equivalent knowledge) in Nursing or related field.
Typically requires 2 years of experience in Research.
Knowledge of Good Clinical Practices, International Conference of Harmonization, FDA Guidance documents, Department of Health and Human Services regulations, standard operating procedures.
Ability to successfully conduct and manage a research study.
Ability to mentor team members and to prepare training plans.
Excellent verbal and written communication skills, organizational and time management skills with ability to work under pressure and meet deadlines.
Ability to problem solve and work independently with a high degree of accuracy and attention to detail.
Must be able to establish a good rapport with patients, investigators and sponsors.
Competency in using Electronic Medical Record (EMR), Microsoft Office Suite, and other computerized programs

Nice To Haves

Oncology clinical trials experience
Clinical Research experience
Oncology experience, Clinical/Medical experience or research related experience, interest in moving into clinical research
Motivated, detail oriented, organized, team player, learns quickly

Responsibilities

Coordinates the conduct of oncology clinical trials with an emphasis on the screening, enrolling, and monitoring of cancer patients at AMG Crystal Lake Oncology/Good Shepherd.
Provides guidance to physicians, clinical staff and research team members.
Coordinates assigned research studies in collaboration with other team members, including but not limited to; study start-up, recruitment, screening, and enrollment of research subjects, development of mechanisms to maximize subject adherence to the research protocol, maintain source documentation, data collection (i.e. development, completion and submission of case report forms (EDC), study drug/device accountability, monitoring of subjects, AE/SAE reporting, study close out, and other elements of study coordination.

Benefits

Advocate Health offers a comprehensive suite of Total Rewards: benefits and well-being programs, competitive compensation, generous retirement offerings, programs that invest in your career development and so much more – so you can live fully at and away from work, including:
Compensation Base compensation listed within the listed pay range based on factors such as qualifications, skills, relevant experience, and/or training
Premium pay such as shift, on call, and more based on a teammate's job
Incentive pay for select positions
Opportunity for annual increases based on performance
Benefits and more Paid Time Off programs
Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
Flexible Spending Accounts for eligible health care and dependent care expenses
Family benefits such as adoption assistance and paid parental leave
Defined contribution retirement plans with employer match and other financial wellness programs
Educational Assistance Program