Clinical Research Associate

Apply for Job Job ID 52660

Location Chicago, Illinois

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Department : MED-Physical Med & Rehab

Salary / Grade : RES /

Target hiring range for this position will be between $75,000-$100,000 per year. Offered salary will be determined by the applicant's education, experience, knowledge, skills and abilities, as well as internal equity and alignment with market data.

Job Summary :

The Clinical Research Associate is responsible for coordinating clinical research-related activities as well as providing clinical research support to the research group. The PA / NP manages activities associated with highly complex clinical research studies including investigator-initiated trials single and multi-center trials and industry-initiated trials. Responsibilities include : performing patients assessments, conducting patient visits, collecting and documenting clinical research data, attending clinical trial conferences and meetings, acting as a liaison between patients and physicians, and acting as a resource to research study patients, physicians, and other / clinical personnel. This individual is the primary contact for all participants and coordinators to access at any time of day. This individual uses advanced communication skills to problem solve complex situations. This individual will provide clinical support and clinical research activities to the PI. This individual acts as a sub investigator on all clinical trials at any given time. The hours for this job are flexible and can be either part-time or full-time.

Specific Responsibilities :

Nurse Practitioner / Physician Assistant

• Become familiar with all protocols conducted at the center. Participates in the initiation of study start-up activities. Contributes to the implementation of protocols and monitors study activities at all stages.
• Evaluates volunteer subjects for potential study qualification in accordance with inclusion / exclusion criteria provided by study sponsor. Assists in patient recruitment as well as acting as a resource for the marketing personnel and
• referring physicians.
• For qualified participants, initiates medical and social histories, physical exam, and physiological measures as indicated in protocol. Records this data in detail. Schedules study visits as required by protocols.
• Ensures appropriate laboratory, x-ray and other diagnostic examinations are
• scheduled and completed per study protocol. Oversees any outside services as required. Conducts all necessary laboratory and imagining tests.
• Performs complete medical histories and physical examinations for qualified participants with emphasis on patient's presenting complaints and findings pertinent to the study. Discriminates between normal and abnormal findings onhistory and physical in order to establish a differential diagnosis. Provides clinical support for divisional research activities within scope of license.
• Review medical, laboratory, and other diagnosis data on study patients. Recognizes conditions beyond the scope of the Nurse Practitioner / Physician Assistant and confers with principal investigator. Makes principal investigator aware of any significant abnormalities. Notifies and follows up with patients as
• appropriate.
• Assists coordinators in assessment of adverse events. Ensures that serious adverse events are reported to the principal investigator and sponsor in a timely manner. Follows up with patients or patient family members in accordance with
• procedures. Knowledge of community resources needed for patients.
• Assists with collection of data requested by protocol. Ensures accuracy of data obtained. Collates and enters data into patient charts, sponsor case report forms,
• and / or remote data entry equipment in a timely and precise manner.
• Ensures that all study drug received in unit is accurately documented and sorted in locked location. Ensures that study drug is maintained in appropriate temperature controlled environment. Verifies that all study drugs is correctly labeled, and packaged. Ensures that appropriate study drug is dispensed to patient
• along with detailed instructions on use. Maintains accurate documentation of each of these along with return study drug.
• When studies require other supplies and / or equipment, will ensure their availability and ensure proper orientation has occurred prior to use.
• Ensures patient compliance with study drug and study visits. Documents all efforts made to retrieve study medication. Notifies sponsor of any deviations from protocol. Whenever possible, obtains permission prior to deviation.
• Schedules routine study reviews with sponsor monitors or appointed sponsor representative. Arranges access to all subject records for the indicated time period
• of review. Allows time to respond to monitor questions and to make corrections to case report forms. Promptly respond to sponsor queries.
• Prepares for and completes close out procedures for terminated studies. Ensures
• all FDA, sponsor, and center regulations have been followed.
• Assist with training of other center personnel who will be directly involved with the assigned study.
• Works with other research coordinators and research assistants to provide back-up, replacement during absences, and follow-up as needed.
• Provides health practices information and education to study patients regarding
• medications, disease, diet, exercise, and any special procedures. Assists patients by providing appropriate referrals to physicians, clinics, or agencies.
• Provides on-call services for study patients during evening and weekend on rotation basis with other coordinators / nurse practitioners / physician assistants.
• Performs diagnostic procedures as required by study protocol.
• Assists in training of center personnel, especially in the clinical assessment skills including blood draw and performing ECGs . Ensures gowns, gloves, goggles, masks and other personal protective equipment are used properly by all staff.
• Participates in other division activity such as special projects, in-service, training, and any other duties assigned by supervisor
• Must take the certification exam within 2 years, or with 1 year if has 1 year previous experience as a research coordinator.

Miscellaneous

Performs other duties as assigned.

Minimum Qualifications : (Education, experience, and any other certifications or clearances)

Minimum Competencies : (Skills, knowledge, and abilities)

Preferred Qualifications : (Education and experience)

Benefits :

At Northwestern, we are proud to provide meaningful, competitive, high-quality health care plans, retirement benefits, tuition discounts and more! Visit us at to learn more.

Work-Life and Wellness :

Northwestern offers comprehensive programs and services to help you and your family navigate life's challenges and opportunities, and adopt and maintain healthy lifestyles.

We support flexible work arrangements where possible and programs to help you locate and pay for quality, affordable childcare and senior / adult care. Visit us at to learn more.

Professional Growth & Development :

Northwestern supports employee career development in all circumstances whether your workspace is on campus or at home. If you're interested in developing your professional potential or continuing your formal education, we offer a variety of tools and resources. Visit us at to learn more .

Northwestern University is an Equal Opportunity Employer and does not discriminate on the basis of protected characteristics, including disability and veteran status. View Northwestern's non-discrimination statement . Job applicants who wish to request an accommodation in the application or hiring process should contact the Office of Civil Rights and Title IX Compliance. View additional information on the accommodations process .

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