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Associate Merck Clinical Trials Jobs in Chicago, IL

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Associate Merck Clinical Trials information

See Chicago, IL salary details

$17

$41

$72

How much do associate merck clinical trials jobs pay per hour?

As of May 28, 2026, the average hourly pay for associate merck clinical trials in Chicago, IL is $41.19, according to ZipRecruiter salary data. Most workers in this role earn between $33.17 and $45.34 per hour, depending on experience, location, and employer.

What is the difference between Associate Merck Clinical Trials vs Clinical Research Coordinator?

AspectAssociate Merck Clinical TrialsClinical Research Coordinator
Required CredentialsBachelor's degree, relevant certifications (e.g., CCRP)Bachelor's degree, often similar certifications
Work EnvironmentPharmaceutical company, clinical trial sites, research labsHospital, research sites, clinics
Employer & IndustryPharmaceutical industry, biotech firmsHealthcare facilities, research organizations
Common Search & ComparisonYesYes

The Associate Merck Clinical Trials role typically involves supporting clinical trial activities within a pharmaceutical company, focusing on drug development and regulatory compliance. In contrast, a Clinical Research Coordinator manages patient recruitment, data collection, and trial logistics at research sites. Both roles require similar educational backgrounds and certifications, but their work environments and specific responsibilities differ, with the Associate Merck Clinical Trials position being more industry-focused and the Clinical Research Coordinator more patient-facing.

What are the most commonly searched types of Merck Clinical Trials jobs in Chicago, IL? The most popular types of Merck Clinical Trials jobs in Chicago, IL are:
Infographic showing various Associate Merck Clinical Trials job openings in Chicago, IL as of May 2026, with employment types broken down into 70% Full Time, 29% Part Time, and 1% Contract. Highlights an 99% Physical, and 1% Hybrid job distribution, with an average salary of $85,677 per year, or $41.2 per hour.

Clinical Research Associate 1

Allen Spolden

Chicago, IL

Other

Medical, Dental, Vision, Retirement, PTO

Posted 20 days ago


Job description

Clinical Research Associate

Responsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee, this position will serve as support for the clinical study team. Essential Duties And Responsibilities Participate and assist in design and preparation of protocols and case report forms. Generate clinical SOPs, policies, charters, and plans according to US and international guidelines. Participate in the evaluation of potential clinical sites according to established criteria of acceptability. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to clinical research functions. Initiate studies performing initiation site visits, arrange for shipment of clinical supplies, case report forms, and other necessary materials. Conduct ongoing study monitoring, including frequent periodic site visits, protocol adherence checks, material handling procedures, inspection of study files, and related monitoring functions. Prepare site visit reports with identification of key accomplishments, key issues for resolution and recommendations for follow-up actions for assigned study sites. Conduct study termination visits, obtain final reports from investigators, and participate in the preparation of final reports for regulatory submission. Assist with the maintenance of clinical archive and electronic files. Other tasks as assigned.

Requirements To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. BA, BS, RN, BSN or equivalent Basic knowledge and adherence to GCPs 1-2 years of clinical research experience or equivalent experience or training Strong attention to detail Ability to multi-task Unquestionable integrity and highest ethical standards Excellent written and verbal communication skills Self-motivated, assertive, and driven Benefits Dental, Medical, Vision, PTO and 401K