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Biotech Clinical Research Jobs in Indiana (NOW HIRING)

Simotechnology

Senior OSI PI Engineer

Indianapolis, IN · On-site

$90 - $120/hr

* Industry Pharma/Biotech/Clinical Research * City Indianapolis * Province Indiana * Country United States Why SimoTech Whatis it like to work at SimoTech? With a strong collaborative teamworkculture ...

Simotechnology

CSV Engineer

Indianapolis, IN · On-site

$90 - $130/hr

* Industry Pharma/Biotech/Clinical Research * City Indianapolis * Province Indiana * Country United States Why SimoTech What is it like towork at SimoTech? With a strong collaborative teamwork ...

IQVIA

CRA 2/Senior CRA

Indianapolis, IN · On-site

$90K - $175K/yr

IQVIA Biotech is seeking CRA 2 and Sr. CRA 1 candidates with onsite monitoring experience in oncology. Join a Team That's Advancing Clinical Research We're looking for a passionate and driven ...

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Biotech Clinical Research information

What is a biotech clinical research?

A Biotech Clinical Research job involves conducting and managing clinical trials to evaluate the safety and efficacy of new drugs, medical devices, or treatments developed by biotechnology companies. Professionals in this field ensure compliance with regulatory guidelines, collect and analyze clinical data, and collaborate with cross-functional teams such as scientists, medical professionals, and regulatory authorities. Their work helps bring innovative therapies to market, improving patient care and advancing medical science.

What are the key skills and qualifications needed to thrive in biotech clinical research?

To thrive in Biotech Clinical Research, you need a solid background in life sciences, clinical trial methodologies, and regulatory compliance, usually supported by a relevant degree such as biology, biochemistry, or pharmacology. Experience with data management systems, statistical analysis software, and certifications like GCP (Good Clinical Practice) are highly valued. Exceptional attention to detail, effective communication, and strong problem-solving abilities are important soft skills for success in this role. These skills ensure clinical trials are conducted accurately, ethically, and efficiently, supporting the advancement of safe and effective biotech products.

What are some common challenges faced by professionals in biotech clinical research?

Professionals in biotech clinical research often encounter challenges such as managing complex regulatory requirements, adapting to frequent protocol amendments, and coordinating among diverse teams across multiple sites. Ensuring high data quality and maintaining strict timelines can also be demanding, especially as studies progress and new discoveries emerge. However, the dynamic nature of the work offers continuous learning opportunities and the reward of contributing to groundbreaking scientific advancements. Team members typically collaborate closely with clinical monitors, project managers, and regulatory affairs specialists to ensure every aspect of the research process runs smoothly.

What does a biotech clinical research do?

A biotech clinical research professional designs, manages, and monitors clinical trials to evaluate the safety and effectiveness of new drugs or therapies. They ensure compliance with regulatory standards, collect and analyze data, and collaborate with healthcare providers and regulatory agencies throughout the development process.

What qualifications do you need to be a biotech clinical researcher?

Biotech clinical researchers typically need a bachelor's degree in a life science, such as biology, chemistry, or related fields. Many roles require experience with clinical trial protocols, data analysis, and familiarity with regulatory requirements; advanced positions may require a master's or doctoral degree. Certifications like Good Clinical Practice (GCP) training can also enhance qualifications.

What are the most commonly searched types of Biotech Clinical Research jobs in Indiana?

The most popular types of Biotech Clinical Research jobs in Indiana are:

What are popular job titles related to Biotech Clinical Research jobs in Indiana?

For Biotech Clinical Research jobs in Indiana, the most frequently searched job titles are:

What job categories do people searching Biotech Clinical Research jobs in Indiana look for?

The top searched job categories for Biotech Clinical Research jobs in Indiana are:

Biotech Clinical Research jobs near you
Infographic showing various Biotech Clinical Research job openings in Indiana as of August 2026, with employment types broken down into 2% As Needed, 72% Full Time, 18% Part Time, and 8% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution.

Senior Clinical Laboratory Associate -- Pharmaceutical (Hybrid -- Indianapolis, IN) Contract (Possible

Pharmavise Corporation

Indianapolis, IN • On-site

$120 - $180/hr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted yesterday

New

Job description

Senior Clinical Laboratory Associate — Pharmaceutical (Hybrid — Indianapolis, IN) Contract (Possible Extension)

Indianapolis, United States

  • Industry Pharma/Biotech/Clinical Research
  • City Indianapolis
  • State/Province Indiana
  • Country United States
About Us

From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology. Our business mission is to ensure our clients exceed their compliance goals while improving patient health and safety. Visit us at www.pharmavise.com and follow us on LinkedIn: https://www.linkedin.com/company/pharmavisecorp

Job Description

Our Fortune 500 global Pharmaceutical client is seeking an experienced Clinical Laboratory Associate.

Job Summary

The Clinical Laboratory Services (CLS) currently has a business need for surge capacity coverage for delivery based Clinical Laboratory Associate (cCLA). This surge capacity model would utilize US-based contractor CLAs (cCLAs) to focus on specific tasks/deliverables. The cCLAs would not be trained on study startup activities but would be the single point of contact representing CLS to study teams and TPOs throughout study maintenance and closeout.

Key Responsibilities
  • Study level project management – including maintenance, data lock and closeout, document flow (review/approvals), budget management
  • Single point of contact for study teams and CLS TPOs
  • Tracking of safety, biomarker, PK and ADA samples as well as imaging and connected devices
  • Query tracking and management
  • Internal & External Engagement - Collaborate with internal business partners regarding CLS processes and business operations
  • Collaborate with business partners and TPOs to ensure data delivery
Other Details

Schedule: 40 hours/week

Work Setup: Hybrid (3 days onsite, 2 days remote – flexible) in Indianapolis, IN

RequirementsRequired Qualifications
  • Master’s and/or PH.D degree in the Medical Science field
  • 10-15+ years of experience in the Project/Program Management field
  • Prior experience in pharma, diagnostics or CRO environment
  • Experience in clinical research or a closely related field
  • Demonstrated ability to communicate clearly
  • Demonstrated attention to detail and organization
  • Skilled in excel for report combining and tracking
Benefits
  • Health Insurance: Eligibility to enroll in medical, dental, and vision insurance plans. You may also participate in a Flexible Spending Account (FSA) or Health Savings Account (HSA) for qualified healthcare and dependent care expenses.
  • Voluntary Benefits: Option to enroll in employee-paid voluntary benefits, including life insurance, short- and long-term disability insurance, and long-term care insurance.
  • 401(k) Plan: Eligibility to participate in the company’s 401(k) retirement plan. Please note, this plan does not include an employer contribution.
  • Commuter Benefits: Eligibility to participate in a commuter benefits program, allowing the use of pre-tax dollars for transit and/or parking expenses.
  • Paid Time Off (PTO): You will accrue two weeks of vacation annually (prorated based on your start date), in addition to sick leave accrued in accordance with applicable state laws. You will also receive 11 company-paid holidays each year.

Note: Benefits will be effective after 30 days.

Pharmavise Corporation is an Equal Opportunity Employer and does not discriminate on the basis of race or ethnicity, religion, sex, national origin, age, veteran disability or genetic information or any other reason prohibited by law in employment.

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