Clinical Research Manager jobs in Illinois
Clinical Research Manager manages the clinical monitoring process and the administration of clinical trials. Supervises CRAs in in-house and on-site monitoring, filing, and clinical trial administration. Being a Clinical Research Manager oversees adherence to SOPs, Good Clinical Practice and FDA regulations. Helps with the development and implementation of clinical processes, procedures, and programs. Additionally, Clinical Research Manager may require a master's degree in nursing. May require ACRP or SOCRA Clinical Research Professional exam completion. Typically reports to a director. The Clinical Research Manager manages subordinate staff in the day-to-day performance of their jobs. True first level manager. Ensures that project/department milestones/goals are met and adhering to approved budgets. Has full authority for personnel actions. To be a Clinical Research Manager typically requires 5 years experience in the related area as an individual contributor. 1-3 years supervisory experience may be required. Extensive knowledge of the function and department processes. (Copyright 2024 Salary.com)
Recently Added Clinical Research Manager jobs
Clinical Research Coordinator III
- DM Clinical Research
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Chicago, IL
FULL_TIME
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Clinical Research Coordinator III
A CRC III will ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. To ensure study enrollment meets or exceeds Sponsors' expectations. To ensure company goals are achieved on a timely basis.
DUTIES & RESPONSIBILITIES- Completing all the DMCR-required training, including but not limited to ICH-GCP Certification and IATA Certification on a timely basis.
- Completing all the relevant training prior to study-start and on a continued basis in a timely manner. This will include but is not limited to:
- Sponsor-provided and IRB-approved Protocol Training
- All relevant Protocol Amendments Training
- Any study-specific Manuals Training, as applicable
- Sponsor-specified EDC and/or IVRS and any other relevant Electronic Systems training.
- Conducting and overseeing study subject visits, and all other relevant protocol-required procedures and documenting these in a timely manner.
- Adherence to ALCOA-C Standards with all the relevant clinical trial documentation.
- Completing and overseeing data entry and query resolution in a timely manner as per internal company guidelines and as per sponsor expectations.
- Demonstration of appropriate and timely follow-up on the action items, at their respective sites.
- Demonstrated understanding, implementation and supervision of protocol-specified laboratory procedures, storage, temperature monitoring, equipment calibration, and laboratory kit inventory for assigned protocols.
- Liaising with the Laboratory team, Data team, Administrative staff, Clinical Investigators, Research Participants and Sponsor/CRO representatives for assigned protocols.
- Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s)
- Maintaining a working knowledge of the recruitment and retention process for their assigned protocol(s) at their respective site(s).
- Ability to train and mentor site staff, as needed
- Supervise visit preparedness for all the relevant sponsor and CRO visits for their assigned protocol(s)
- Demonstration of appropriate and timely follow-up on the action items, at their respective sites.
- Maintaining a working knowledge of the most recent versions of the Study Protocols, Informed consents, Study Manuals, and all the other relevant study-related documents that are utilized and implemented for the assigned protocols at their respective site(s).
- Maintaining a working knowledge of Study Participants’ Scheduling, Visit Tracking, Stipends and Transportation by liaising with the Administrative team.
- Maintaining a working knowledge of the Essential Clinical Trial Documents and maintenance of the Investigator Site Binders for their assigned protocol(s) at their respective site(s)
- Oversee reporting of all Adverse and Serious Adverse Events and any other relevant Safety Information to the appropriate authorities per internal company guidelines, Sponsor, IRB, and ICH-GCP Guidelines.
- Striving to meet Sponsor subject enrollment goals for their assigned protocols at their respective site(s).
- Being prepared for and available at all required company meetings.
- Submitting required administrative paperwork per company timelines.
- Occasionally attending out-of-town Investigator Meetings
- Conduct patient consent discussions and ensure comprehension of medical procedures, risks, benefits, and alternatives
- Provide clear explanations of study protocols and ensure patients' understanding before obtaining their consent
- Facilitate effective communication between patients, healthcare providers, and research staff
- Any other matters as assigned by management
KNOWLEDGE & EXPERIENCE
Education:- High School Diploma or equivalent required
- Bachelor's degree preferred
- Foreign Medical Graduates preferred
- Minimum of 5 years experience in Clinical Research
- Supervisory experience preferred
- Wide therapeutic range of clinical trials experience preferred
- Regulatory research experience is a plus
- ACRP or equivalent certification is preferred
- Goals-driven while continuously maintaining quality.
- Must be detailed-oriented, proactive, and able to take initiative.
- Must have strong written and communication skills.
- Must have excellent customer service skills.
- Proficient communication and comprehension skills both verbal and written in the English language are required.
- Proficient Bi-lingual (English/Spanish) communication and comprehension skills both in verbal and written are preferred.
- 3 Days Ago
Medical Research Office Manager
- MetroMed Clinical Trials
-
Chicago, IL
FULL_TIME
- Job description MetroMed Clinical Trials is seeking a clinical office manager. He/she will provide customer-focused leadership in managing multiple Phase II through Phase IV clinical research trials a...
- 30 Days Ago
Clinical Research Coordinator
- Revival Research Institute, LLC
-
ELGIN, IL
FULL_TIME
- Unique opportunity to make an Impact in the healthcare industry… Revival Research Institute, LLC was established in 2015, and headquartered in the Metro Detroit Region, and has been growing ever since...
- 2 Months Ago
Clinical Research Coordinator (CRC)
- Center for Clinical and Translational Science
-
Chicago, IL
FULL_TIME
- Clinical Research Coordinator, UIC Center for Clinical and Translational ScienceThe Clinical Research Coordinator works within the CCTS Clinical Research Center and is responsible for managing and coo...
- 15 Days Ago
Senior Clinical Research Associate
- OnPoint Clinical Staffing Services
-
Chicago, IL
FULL_TIME
- Job DescriptionSenior CRAResponsibilities include:* All aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, writing of clinical t...
- 1 Month Ago
Clinical Research Manager
- Ann & Robert H. Lurie Children's Hospital of Chicago
-
Chicago, IL
FULL_TIME
- Ann & Robert H. Lurie Children's Hospital of Chicago provides superior pediatric care in a setting that offers the latest benefits and innovations in medical technology, research and family-friendly d...
- 20 Days Ago
Clinical Research Manager jobs at Popular Companies
Clinical Research Manager 182825
- Medix™
-
- We are looking to add a Clinical Research Manager to our growing team. This is a full time onsite position with a compet...
- 4/26/2024 12:00:00 AM
Clinical Research Manager
- Triton Medical Robotics
-
Burlingame, CA
- Triton Medical Robotics, a division of Neptune Medical, is an innovative, venture capital funded medical device startup ...
- 4/25/2024 12:00:00 AM
Clinical Research Manager (Clinical Research Regulatory)
- Thomas Jefferson University
-
Philadelphia, PA
- Responsibilities The Clinical Research Coordinator IV trains research staff, supervises staff and oversees clinical tria...
- 4/25/2024 12:00:00 AM
Clinical Research Manager
- Colgate-Palmolive
-
Piscataway, NJ
- No Relocation Assistance Offered # 159181 - Piscataway, New Jersey, United States **Who We Are** Colgate-Palmolive Compa...
- 4/25/2024 12:00:00 AM
Clinical Research Manager
- Houston Journal of Health Law & Policy
-
Houston, TX
- Description Oversees investigator-initiated and sponsored clinical research projects. Manages graduate students, post-do...
- 4/23/2024 12:00:00 AM
Clinical Research Manager
- International Spine Pain & Performance Center
-
Washington, DC
- The International Spine, Pain & Performance Centeris currentlyseeking an ExperiencedClinical Research Manager! Internati...
- 4/22/2024 12:00:00 AM
Clinical Research Manager
- Triton Medical Robotics
-
Burlingame, CA
- Triton Medical Robotics, a division of Neptune Medical, is an innovative, venture capital funded medical device startup ...
- 4/22/2024 12:00:00 AM
Clinical Research Manager (Ophthalmology)
- Northwestern University
-
Chicago, IL
- Department: MED-Ophthalmology Salary/Grade: EXS/7 Job Summary: Oversees the Department of Ophthalmology research program...
- 4/22/2024 12:00:00 AM
About Illinois
Illinois (/ˌɪlɪˈnɔɪ/ (listen) IL-ih-NOY) is a state in the Midwestern and Great Lakes region of the United States. It has the fifth largest gross domestic product (GDP),
the sixth largest population, and the 25th largest land area of all U.S. states. Illinois is often noted as a microcosm of the entire United States. With Chicago in northeastern Illinois, small industrial cities and immense agricultural productivity in the north and center of the state, and natural resources such as coal, timber, and petroleum in the south, Illinois has a diverse economic base, and is a major transportation hu...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Manager jobs
$101,515 to $134,499
Most Popular Cities in Illinois for Clinical Research Manager Jobs
What does a Clinical Research Manager do?
Clinical Research Manager in Richland, WA
Clinical research managers must plan every phase of research programs, from initial concept through product development and clinical trials to submission for approval by the U.S.
November 27, 2019
Clinical Research Manager in Spartanburg, SC
Research is both the foundation and the future of medicine.
December 17, 2019
Clinical Research Manager in Vallejo, CA
When transitioning into the clinical research field from a science background, it is good to know what experience you have, what positions you are interested in, and what careers are most appropriate for your background.
December 19, 2019