Labcorp Posted September 29, 2026

Study Technician - Dose Formulations (Early Talent)

Greenfield, Indiana, United States of America FULL_TIME
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Labcorp is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world’s most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you’ll have the opportunity to do meaningful work, grow your career and make a real impact on people’s health around the world. Together, we’re improving health and improving lives.

Labcorp is seeking a Study Technician - Dose Formulations to join our team in Greenfield, IN!

Work Schedule:

During training: 8:00am-4:30pm Monday-Friday for approximately 2 months.

Once training is completed this position offers a 4-day work week!!

Job Summary:

The Study Technician – Dose Formulation is an entry-level laboratory role responsible for learning and supporting the preparation of test materials for dose administration. This position operates in compliance with Standard Operating Procedures (SOPs), Good Laboratory Practices (GLPs), and applicable regulatory guidelines. The role provides hands-on training in scientific techniques, data documentation, and study support activities within a regulated laboratory environment.

Job Responsibilities:

Learn to review and interpret study protocols to support accurate test material formulation procedures.

Assist in conducting study tasks in compliance with protocols, SOPs, and GLPs.

Accurately collect, document, and maintain laboratory data (both manual and electronic).

Perform basic study-related calculations and formulation techniques under supervision.

Support study setup, execution, and data organization efforts.

Assist with quality checks and respond to QA audits as needed.

Develop effective communication skills with internal teams and, when appropriate, external clients.

Operate and maintain laboratory equipment relevant to assigned tasks.

Prepare laboratory reagents, vehicles, diets, solutions/suspensions, and capsules according to protocols.

Assist with sample handling, including storage, tracking, and disposition of dose materials.

Support formulation verification processes.

Follow procedures for the safe handling of test materials and maintain compliance with safety standards.

Maintain a clean, organized, and safe laboratory workspace.

Identify and report deviations or issues that may impact study integrity.

Escalate concerns to Study Directors, Principal Investigators, or management as appropriate.

Participate in daily workload planning and manage multiple assignments effectively.

Collaborate within a team environment and contribute to shared goals.

Support continuous improvement and process enhancement initiatives.

Perform additional duties as assigned.

Minimum Qualifications:

Bachelor’s degree (BS/BA) in Chemistry, Biology, or a related scientific field

Additional Job Standards:

Basic computer proficiency (e.g., Microsoft Word and Excel)

Strong attention to detail and data accuracy

Ability to learn technical laboratory procedures

Effective communication and teamwork skills

Core competencies: Customer Focus

Innovation & Adaptability

Scientific & Process Excellence

Collaboration

Results Orientation

This is a future hire position with an future start date.  The ideal candidate would be available to start in May 2027 through October 2027. Candidates who have recently completed a degree or will complete a degree within the next academic year may find this opportunity aligns well with their career goals. #LifeatLabcorp

Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees are only eligible to participate in the 401(k) Plan. For more detailed information, please  click here .

Relocation assistance available.

Labcorp is proud to be an Equal Opportunity Employer:

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.

We encourage all to apply

If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our  accessibility site  or contact us at  Labcorp Accessibility. For more information about how we collect and store your personal data, please see our  Privacy Statement .

Job details

Seniority
Not listed
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Greenfield, Indiana, United States of America
Employment type
FULL_TIME

How this role compares

Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.

We currently track 2648 comparable Manufacturing & CMC roles across 168 biopharma companies.

2648Comparable roles tracked
2485Currently active
168Companies hiring similar roles
61Countries represented

Salary context

688 of 2648 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Highest disclosed · Head of Analytical Development · ModernaTX, Inc. $272,200/yr – $490,100/yr
Peer group range $0 – $381,150 (median $121,696)

Where these roles are based

Top locations among the 2648 comparable roles

United States1278
India155
Germany139
France127
Ireland93
China80

+ 55 more countries

Seniority mix

1242 of 2648 peers have a known seniority level

Senior343
Manager280
Intern/Fellow/Postdoc171
Associate145
Principal94
Associate Director90
Director77
Senior Director35
Executive/VP7

Therapeutic area mix

19 of 2648 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease12
Oncology3
Rare Disease2
Respiratory1
Dermatology & Aesthetics1

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The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

40%similar
AstraZeneca New Haven, Connecticut, United States of America
Same function Same country
40%similar
40%similar
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Same function Same country
40%similar
Lilly Indianapolis, Indiana, United States of America Intern/Fellow/Postdoc
Same function Same country
40%similar
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Same function Same country
40%similar
Lilly Indianapolis, Indiana, United States of America Director
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Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

40%
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Function Therapeutic area Seniority Country
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Function Therapeutic area Seniority Country
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Director, Site Lead Combination Product Development, R&D
AbbVie · North Chicago, IL · Director
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.