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Oncore Jobs in Michigan (NOW HIRING)

McLaren

Clinical Research Coordinator II

Detroit, MI · On-site

$24 - $32/hr

Maintain logs, including tracker submissions and update the CTO Oncore database in a timely manner according to CTO SOPs. * Design systems for coordinating, compiling and submission of data; design ...

McLaren

Clinical Research Coordinator II

Detroit, MI · On-site

$24 - $32/hr

Maintain logs, including tracker submissions and update the CTO Oncore database in a timely manner according to CTO SOPs. * Design systems for coordinating, compiling and submission of data; design ...

University of Michigan

RESEARCH ASST I (TEMP)

Ann Arbor, MI · On-site

$18.75 - $26/hr

Additional responsibilities include entering research data into electronic data capture systems such as OnCore, MQUARK, SharePoint, REDCap, and MyDataHelps, as well as maintaining paper case report ...

All JobsOncore JobsOncore Jobs in Michigan

Oncore information

See Michigan salary details

$213.5K

$328.4K

$348.6K

How much do oncore jobs pay per year?

As of Aug 7, 2026, the average yearly pay for oncore in Michigan is $328,373.00, according to ZipRecruiter salary data. Most workers in this role earn between $323,400.00 and $348,600.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Oncore position?

To thrive in an Oncore Clinical Research Associate role, a background in life sciences, clinical trial monitoring experience, and knowledge of regulatory guidelines such as GCP are essential. Proficiency in electronic data capture (EDC) systems, trial management software, and certifications like ACRP or SOCRA are often required. Excellent organizational skills, attention to detail, and effective communication help candidates excel in multi-site coordination and team settings. These capabilities ensure the smooth execution, compliance, and high-quality outcomes of clinical research studies.

What does an Oncore Clinical Research Associate do?

A typical day for an Oncore Clinical Research Associate involves monitoring ongoing clinical trials, ensuring they are conducted according to protocol, and reviewing data for accuracy and compliance. You'll frequently interact with study site staff, coordinate with investigators, and document findings in clinical trial management systems like OnCore. The role may also include onsite visits, remote monitoring, and regular meetings with sponsors or regulatory teams. Timely communication and attention to protocol details are crucial, making it a dynamic and collaborative work environment with opportunities to learn and grow within the clinical research field.

What is an Oncore?

An Oncore job typically refers to a position within the Oncore platform, a workforce management system used for contingent labor and project-based work. These jobs can vary across industries and may include contract, temporary, or gig-based roles. Oncore helps businesses efficiently manage and pay their contingent workforce while ensuring compliance with labor regulations. If you are hired for an Oncore job, you may work as an independent contractor or temporary employee depending on the arrangement.

What are popular job titles related to Oncore jobs in Michigan? For Oncore jobs in Michigan, the most frequently searched job titles are:
What job categories do people searching Oncore jobs in Michigan look for? The top searched job categories for Oncore jobs in Michigan are:
Oncore jobs near you
Infographic showing various Oncore job openings in Michigan as of August 2026, with employment types broken down into 2% Internship, 90% Full Time, 6% Part Time, and 2% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $328,373 per year, or $157.9 per hour.

Clinical Research Coordinator II

McLaren

Detroit, MI • On-site

$24 - $32/hr

Full-time

Re-posted 25 days ago

Job description

Provide study coordinator/data management/regulatory specialist support to the Clinical Trials Office (CTO). Manage independent assignment, providing excellent customer support and guidance in the clinical trials arena.
Responsibilities:
  • Assure all study requirements are met and documented and meet both internal and external regulations in accordance with protocol guidelines.
  • Maintain logs, including tracker submissions and update the CTO Oncore database in a timely manner according to CTO SOPs.
  • Design systems for coordinating, compiling and submission of data; design workflow processes and participate in quality assurance measures; coordinate site visits.
  • Manage all patient and/or protocol data as assigned and respond to queries in a timely fashion.
  • Schedule and participate in monitoring visits and participate in multidisciplinary team program meetings as required.

• Bachelor's degree required or equivalent combination of education and experience.
• Medical and/or science experience/education preferred.
• Clinical research certification preferred.
Equal Opportunity Employer of Minorities/Females/Disabled/Veterans
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About McLaren

Sourced by ZipRecruiter

McLaren Group is globally renowned as one of the world’s most illustrious high-technology brands. Since the formation of McLaren Racing in 1963, McLaren has been pioneering and innovating in the competitive world of Formula 1, forging a formidable reputation which has seen the racing team win 20 World Championships and over 180 races. The Group has built on its successful racing expertise and diversified to include a global, high-performance sports car business, McLaren Automotive, and a game-changing technology and innovation business, McLaren Applied. Despite the broadening of the group’s business interests, McLaren’s goal remains singular: we exist to win in everything we do.

Industry

Automobile dealers and manufacturing

Company size

10,000+ Employees

Headquarters location

Woking, Surrey, GB

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