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Study Monitor Jobs in Indiana (NOW HIRING)

Corteva Agriscience

Study Monitor

Indianapolis, IN · On-site

Product Chemistry is thrilled to announce an exciting opportunity for a Product Chemistry Study Monitor. In this role, you will be responsible for coordinating and executing studies at global ...

Inotiv

Study Director III, Toxicology

Mount Vernon, IN · On-site

Monitor the progress of studies and after consultation with senior staff, report the results to the sponsor * Participate in in-house training programs for the technical staff * Conduct literature ...

Labcorp

Global CDx Study Manager

Indianapolis, IN · On-site

Establish and monitor performance metrics, implementing corrective actions as needed. * Provide pre ... Day-to-Day Study Operations (≈80%): * Coordinate and host CRA visits and client audits. * Develop ...

Labcorp

Global CDx Study Manager

Indianapolis, IN · Hybrid

Establish and monitor performance metrics, implementing corrective actions as needed. * Provide pre ... Day-to-Day Study Operations (80%): * Coordinate and host CRA visits and client audits. * Develop ...

Diocese of Gary

English Teacher-Full Time

Merrillville, IN · On-site

$44K - $60K/yr

Promotes Catholic Identity and nurtures the education of students by planning and tailoring courses of study; monitoring, assisting with, and correcting, academic efforts; providing a safe ...

Diocese of Gary

Substitute Teaching

Merrillville, IN · On-site

Promotes Catholic Identity and nurtures the education of students by planning and tailoring courses of study; monitoring, assisting with, and correcting, academic efforts; providing a safe ...

Ivy Tech

Federal Work Study Off-Campus

Indianapolis, IN · On-site

$18/hr

We are "higher education at the speed of life!" Through Federal Work Study, we partner with community organizations to create meaningful employment opportunities for students. These jobs not only ...

Ivy Tech

Federal Work Study Off-Campus

Indianapolis, IN · On-site

$18/hr

We are "higher education at the speed of life!" Through Federal Work Study, we partner with community organizations to create meaningful employment opportunities for students. These jobs not only ...

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All JobsStudy Monitor JobsStudy Monitor Jobs in Indiana

Study Monitor information

See Indiana salary details

$15.9K

$72.5K

$129.4K

How much do study monitor jobs pay per year?

As of Jun 24, 2026, the average yearly pay for study monitor in Indiana is $72,479.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,247.00 and $106,867.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Study Monitor position, and why are they important?

To thrive as a Study Monitor, you need a strong understanding of clinical trial protocols, regulatory guidelines (such as GCP), and data integrity principles, typically supported by a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like ACRP or SOCRA are commonly expected. Excellent attention to detail, strong organizational skills, and effective communication are crucial soft skills. These competencies ensure high-quality study oversight, compliance with regulations, and smooth collaboration among clinical research teams.

What are some common challenges Study Monitors face during clinical trials?

Study Monitors often encounter challenges such as ensuring consistent protocol adherence across multiple sites, managing discrepancies in data, and navigating tight timelines for site visits and reporting. They must adapt quickly to evolving regulatory requirements and effectively communicate any issues or deviations to investigators and sponsors. Being proactive in identifying potential risks and fostering strong relationships with site staff can help minimize these challenges. As a result, successful Study Monitors need to be resourceful, detail-oriented, and skilled at balancing regulatory compliance with practical problem-solving in dynamic trial environments.

What is a Study Monitor job?

A Study Monitor, also known as a Clinical Research Associate (CRA), is responsible for overseeing clinical trials to ensure they comply with regulatory guidelines, study protocols, and ethical standards. They monitor site activities, review data accuracy, and ensure participant safety. Study Monitors work closely with investigators, site staff, and sponsors to ensure the integrity of trial results and adherence to Good Clinical Practice (GCP) guidelines.

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Study Monitor jobs near you
Study Monitor

Study Monitor

Corteva Agriscience

Indianapolis, IN • On-site

Full-time

Medical, Retirement, PTO

Posted 14 days ago

Job description

Who We Are and What We Do
At Corteva Agriscience, you will help us grow what's next. No matter your role, you will be part of a team that is building the future of agriculture - leading breakthroughs in the innovation and application of science and technology that will better the lives of people all over the world and fuel the progress of humankind.
Product Chemistry is thrilled to announce an exciting opportunity for a Product Chemistry Study Monitor. In this role, you will be responsible for coordinating and executing studies at global contract labs that are required for crop protection and biological registrations, both for active ingredients and plant protection products. Additionally, you will troubleshoot any analytical challenges that arise with methods or studies. As a valued member of our team, you will have the chance to collaborate with talented and dedicated colleagues, while also developing and advancing your career
What You'll Do:
  • Request quotes from multiple contract labs
  • Execute product chemistry studies for all types of test materials needed for global registrations
  • Partner closely with product chemistry subject matter experts (PC SMEs)
  • Interact weekly or monthly with contract labs to review on-going studies and prioritize workloads if needed
  • Interpret analytical data. Troubleshoot and implement solutions for experimental challenges as needed to ensure study requirements are met.
  • Ensure that all data are generated and documented in a manner consistent with GLP regulations, SOPs, best practices, and study protocols.
  • Partner closely with many different stakeholders and navigating in a fast-paced environment.
  • Communicate to PC SMEs often on timelines

What Skills You Need:
  • A minimum of a bachelor's degree is required. Degree discipline in Chemistry or a related science is preferred.
  • A minimum of two years relevant work experience with chromatography and analytical chemistry techniques is preferred.
  • Thrive in a fast-paced, multi-tasking, and customer-focused environment
  • Adaptable and responsive to urgent or shifting project priorities
  • Strong project management skills
  • Highly organized with time management abilities
  • Excellent interpersonal and communication skills; able to engage effectively with diverse stakeholders and peers
  • Committed to promoting and upholding environmental health and safety standards
  • Analytical technique background in LC, GC, LC/MS, or GC/MS
  • GLP Certification is recommended but not mandatory

Benefits - How We'll Support You:
  • Numerous development opportunities offered to build your skills.
  • Be part of a company with a higher purpose and contribute to making the world a better place.
  • Health benefits for you and your family on your first day of employment.
  • Four weeks of paid time off and two weeks of well-being pay per year, plus paid holidays.
  • Excellent parental leave which includes a minimum of 16 weeks for mother and father.
  • Future planning with our competitive retirement savings plan and tuition reimbursement program.
  • Learn more about our total rewards package here - Corteva Benefits.
  • Check out life at Corteva! www.linkedin.com/company/corteva/life.

Are you a good match? Apply today! We seek applicants from all backgrounds to ensure we get the best, most creative talent on our team.
Corteva Agriscience is an equal opportunity employer. We are committed to embracing our differences to enrich lives, advance innovation, and boost company performance. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, military or veteran status, pregnancy related conditions (including pregnancy, childbirth, or related medical conditions), disability or any other protected status in accordance with federal, state, or local laws.
Benefits - How We'll Support You:
  • Numerous development opportunities offered to build your skills
  • Be part of a company with a higher purpose and contribute to making the world a better place
  • Health benefits for you and your family on your first day of employment
  • Four weeks of paid time off and two weeks of well-being pay per year, plus paid holidays
  • Excellent parental leave which includes a minimum of 16 weeks for mother and father
  • Future planning with our competitive retirement savings plan and tuition reimbursement program
  • Learn more about our total rewards package here - Corteva Benefits
  • Check out life at Corteva! www.linkedin.com/company/corteva/life

Are you a good match? Apply today! We seek applicants from all backgrounds to ensure we get the best, most creative talent on our team.
Corteva Agriscience is an equal opportunity employer. We are committed to embracing our differences to enrich lives, advance innovation, and boost company performance. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, military or veteran status, pregnancy related conditions (including pregnancy, childbirth, or related medical conditions), disability or any other protected status in accordance with federal, state, or local laws.

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