Clinical Research Associate II - Cross-TA Monitoring
ICON Clinical Research
ICON Clinical Research is actively seeking a Clinical Research Associate in Chicago, IL. In this role, you will serve as the primary point of contact between investigational sites and the sponsor while ensuring compliance and conducting site visits. The ideal candidate should have a Bachelor’s degree in Life Sciences, 2+ years of relevant experience, and strong knowledge of ICH-GCP. ICON offers a competitive salary, various health insurance options, and benefits promoting work-life balance. #J-18808-Ljbffr
- ...ICON is seeking a Clinical Research Associate to act as the primary point of contact between investigational sites and the sponsor in Chicago... ...Sciences or is a qualified RN, with 2+ years of on-site monitoring experience in the pharmaceutical or CRO industry. This position...Suggested
- ...A pharmaceutical company in Chicago is seeking a Clinical Research professional to provide support for clinical trials and assist in the... ...excellent communication skills. Responsibilities include site monitoring, report preparation, and maintaining clinical archives. The...Suggested
$66.8k - $120k
...Environmental Conditions Office Job Description Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We... ...to perform and coordinate all aspects of the clinical monitoring and site management process. As a Clinical Research...SuggestedTemporary workWork at officeRemote workHome officeFlexible hoursNight shift- Clinical Research Associate - Oncology - Chicago ICON plc is a world-leading healthcare intelligence... ...selection, initiation, routine monitoring, and close-out Ensure site compliance... ...(as applicable) Collaborate with cross-functional partners including CTAs, LTMs...SuggestedLocal areaVisa sponsorshipFlexible hours
- ...Clinical Research Associate – Oncology – Chicago ICON plc is a world‑leading healthcare intelligence... ...including selection, initiation, routine monitoring, and close‑out Ensure site compliance... ...(as applicable) Collaborate with cross‑functional partners including CTAs, LTMs...SuggestedLocal areaVisa sponsorshipFlexible hours
- ...Clinical Research Associate - Cross Therapeutic Area - Chicago ICON plc is a world-leading healthcare intelligence and clinical research organization... ...site visits, including selection, initiation, routine monitoring, and close-out Ensure site compliance with ICH-GCP,...Local areaVisa sponsorshipFlexible hours
$91.34k - $114.17k
...divh2Clinical Research Associate - Oncology - Chicago/h2pICON plc is a world... ...healthcare intelligence and clinical research organization. Were... ...selection, initiation, routine monitoring, and close-out/liliEnsure... ...applicable)/liliCollaborate with cross-functional partners...Work experience placementLocal areaVisa sponsorship- ...UChicago Medicine is seeking a Neurodiagnostic Specialist II in Chicago. This full-time position involves independent preparation of patients for EEG monitoring, the ability to report on EEG data, and performing specialty procedures with minimal supervision. Candidates...Full timeAfternoon shift
$100k - $120k
...Zachary Piper Solutions is seeking a Clinical Research Associate (CRA) for an opportunity in Chicago, Illinois. The CRA will conduct site and study visits, performing monitoring activities across multiple trials for a leading Clinical Research Organization. Qualified...Remote work$71.9k - $189k
...IQVIA Argentina is seeking a Clinical Research Associate in Oak Brook, Illinois. This full-time role requires at least 2 years of on-site monitoring experience and a Bachelor's Degree in a scientific discipline or health care. The responsibilities include site management...Full time- ...Advanced Clinical in Chicago is seeking a Senior Clinical Research Associate (Sr. CRA) to conduct monitoring activities at clinical trial sites. This position requires ensuring that the studies comply with protocols and regulatory requirements while mentoring other staff...Work at officeWork from home
- ...Job Title Responsible for providing Clinical Research support for all clinical trials. Job Information Date Opened 12/14/2023... ...forms, and other necessary materials. Conduct ongoing study monitoring, including frequent periodic site visits, protocol adherence...Full timeWork experience placement
- ...Clinical Research Associate - Early Development Multi Therapeutic - Midwest Region... ...selection, initiation, routine monitoring, and close-out Ensure... ...) Collaborate with cross-functional partners including... ...early development Phase I/II clinical studies, across multiple...Local areaVisa sponsorshipFlexible hours
$101.6k - $169.3k
...IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology, cardiovascular, renal, metabolic, CNS, Obesity (GLP-... ...NASH, dermatology, or respiratory: Job Overview: Perform monitoring and site management work to ensure that sites are conducting...Full timePart timeLocal areaImmediate startWorldwide$71.9k - $189k
IQVIA Argentina is seeking a Clinical Research Associate in Oak Brook, Illinois. This full-time role requires at least 2 years of on-site monitoring experience and a Bachelor's Degree in a scientific discipline or health care. The responsibilities include site management...Full time$54.4k - $111.5k
A national financial institution is seeking a Credit Analyst II to support underwriting and monitoring credit for asset-based lending. This role requires building proficiency in analytics, risk assessment, and addressing compliance issues. Candidates should possess a Bachelor...- ...pipeline by striving for excellence in clinical research, turning science into medicine for our... ...site training, routine, and site closure monitoring activities with compliance to the... ...applicable policies. Demonstrate strong cross-functional collaboration skills among internal...Remote jobContract workTemporary workLocal area
- ...ICON Clinical Research in Chicago is seeking a Clinical Research Associate to serve as the primary contact between investigational sites and the sponsor. Responsibilities... ..., ensuring compliance with regulations, and monitoring patient safety. The ideal candidate will have a...
- ...ICON Strategic Solutions is seeking a Clinical Research Associate in Chicago. The role involves conducting site visits, ensuring compliance, and monitoring patient safety. Ideal candidates will have a Bachelor’s degree or be qualified RNs, along with at least 2 years of...
- ...Overview The Clinical Research Associate (CRA) role focuses on supporting clinical trials, regulatory... ...study tracking tools, documentation, monitoring visits, and assisting in audits or inspections... ...an ability to work effectively in a cross-functional setting with a variety of...Work at officeImmediate startRemote work
- ...Purpose: The Site and Monitoring Health Lead (SMH Lead)... ...safeguard the quality of clinical trial execution at... ...directed by the client Associate Director (or above), Site... ...Management/Clinical Research Organization (CRO) to... ...collaboratively with cross-functional teams Builds...Local area
- ...Under the direction of the Clinical Nurse Manager, provides nursing care in accordance with departmental and hospital... ...state. BLS Certification - American Heart Association (Healthcare Provider) or American Red Cross (Healthcare Provider) required, must be current....ReliefImmediate start
$193.5k - $406.5k
...strive to build an environment where our associates are in the driver's seat of their... ...lead product Consumer platform, Credit Monitoring and Identity for TransUnion's Consumer Solutions... ...and Global markets Collaborate with cross-functional counterparts in Global Technology...Full timeWork experience placementWork at officeFlexible hours2 days per week- ...to 40 feet. Lifting Trash box, challenged passengers into their seats, assistive devices, emergency equipment. Up to 40 lbs. Crossing lot, up and down bus aisle, around exterior of bus Sitting up to 2-3 hours Climbing steps in and out of bus multiple times a...Contract workWork at officeEarly shift
- ...Join Our CRA Team in Cincinnati, Ohio! The Clinical Research Associate position at Medpace offers the unique opportunity to have an exciting... ...Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with...Contract workWork experience placementWork at officeLocal areaImmediate startRemote workWork from homeHome officeFlexible hours
$100k - $120k
...Piper Companies is currently seeking aClinical Research Associate (CRA) for an opportunity in Chicago, Illinois (IL).The Clinical Research Associate (CRA) will participate in... ...site and study visits and perform all site monitoring activities across multiple study Responsible...Remote work- ...Senior Clinical Research Associate (Sr. CRA) is responsible for: Conducting monitoring activities at assigned clinical trial site(s) Verifying the adequacy, reliability, and quality of data collected at clinical sites Ensuring the conduct of the study is in compliance...Fixed term contractInterim roleLocal areaWork from home
$120k - $135k
...Piper Companies is actively seeking Clinical Research Associates to join a toptier CRO with a proven track record of excellence, trusted by... ...evaluations Work collaboratively with the team to ensure monitoring activities meet study requirements Conduct on site...Remote work- ...Title: Clinical Research Associate *This role is located in either Chicago or Wisconsin The Clinical Research Associate (CRA) has local... ...contact with the study site and has the responsibility for monitoring the study conduct to ensure proper delivery of the study....Hourly payTemporary workLocal areaRemote work
- ...Position: Senior Clinical Research Associate (level dependent on experience) Location: Chicago, IL Job Id: CRA Ongoing IL # of Openings: 1 Senior... .... Conducts study site visits (pre-study, initiation, monitoring, and close-out) and completes site visit deliverables within...Local areaRemote workWork from homeHome office
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