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Preclinical Project Manager Jobs in Indiana (NOW HIRING)

Associate Oligonucleotide Chemist

Indianapolis, IN · On-site

$23.25 - $30.50/hr

... management of disease, and give back to our communities through philanthropy and volunteerism. We ... Collaborate with chemists and scientists across fields to deliver on shared project goals through ...

... management of disease, and give back to our communities through philanthropy and volunteerism. We ... preclinical data is essential. Strong interpersonal skills and the ability to excel in a highly ...

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Preclinical Project Manager information

How does a Preclinical Project Manager typically coordinate with cross-functional teams during a drug development project?

A Preclinical Project Manager works closely with scientists, regulatory affairs, toxicology, and external vendors to ensure all preclinical studies are executed on time and within budget. They facilitate regular meetings to align project milestones, address challenges, and manage documentation for compliance. Effective communication and proactive issue resolution are key, as the role often requires balancing the needs of diverse stakeholders while keeping the overall project timeline on track.

What are the key skills and qualifications needed to thrive as a Preclinical Project Manager, and why are they important?

To thrive as a Preclinical Project Manager, you need a solid background in life sciences or pharmaceutical research, often with an advanced degree and experience managing preclinical studies. Familiarity with project management tools, regulatory guidelines (such as GLP), and software like Microsoft Project or similar platforms is typically required. Strong organizational, leadership, and communication skills are vital for coordinating cross-functional teams and ensuring project timelines are met. These skills and qualifications are crucial for efficiently advancing drug candidates through preclinical development while ensuring compliance and project success.

What does a Preclinical Project Manager do?

A Preclinical Project Manager oversees the planning, coordination, and execution of preclinical research projects that typically involve laboratory and animal studies before clinical trials in humans can begin. They work closely with scientists, regulatory teams, and stakeholders to ensure that studies are conducted according to protocols, timelines, and regulatory requirements. Their responsibilities include managing budgets, resources, and communication among various teams to advance drug candidates or medical devices through the early stages of development. Effective Preclinical Project Managers help ensure that projects meet scientific and business objectives, and that all data generated is reliable and compliant with industry standards.
What are popular job titles related to Preclinical Project Manager jobs in Indiana? For Preclinical Project Manager jobs in Indiana, the most frequently searched job titles are:
Infographic showing various Preclinical Project Manager job openings in Indiana as of June 2026, with employment types broken down into 93% Full Time, 5% Part Time, and 2% Contract. Highlights an 90% Physical, 4% Hybrid, and 6% Remote job distribution.
Principal Scientist - Synthetic Chemist / Peptide Therapeutics (Indianapolis)

Principal Scientist - Synthetic Chemist / Peptide Therapeutics (Indianapolis)

Lilly

Indianapolis, IN • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 23 days ago


Eli Lilly and Company rating

8.8

Company rating: 8.8 out of 10

Based on 62 frontline employees who took The Breakroom Quiz

11th of 71 rated pharmaceutical


Job description

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.

This is a lab-based position in the Peptide Therapeutics Team within Biotechnology Discovery Research in Indianapolis. The individual will synthesize, purify, characterize, and optimize therapeutic peptides and bioconjugates in support of preclinical drug discovery and development efforts. This role requires a skilled bench scientist who contributes meaningfully to structure-activity relationship (SAR) campaigns - not only generating target molecules but also analyzing data, interpreting results, and making design recommendations that help advance projects from concept toward candidate selection.

The individual will work closely with fellow chemists and cross-functional partners across such areas as Discovery Chemistry, Genetic Medicines, Therapeutic Area teams, ADME, and Bioproduct Development. Skilled synthetic chemists with limited peptide chemistry experience and deeper expertise in areas such as small molecules, oligonucleotides, or protein conjugation are welcome to apply.

KEY OBJECTIVES/DELIVERABLES:

  • Synthesis & SAR Contribution: Utilize state-of-the-art synthesis techniques to drive compound generation, including peptide synthesis, purification, and characterization. Propose alternative synthetic strategies and overcome synthetic challenges. Analyze and interpret structure-activity relationships to make informed design recommendations that move projects forward.

  • Data Integration & Problem-Solving: Apply a data-driven approach to experimental planning. Search and integrate relevant chemical and scientific literature to inform design choices. Develop growing expertise in areas such as physicochemical characterization and pharmaceutical developability as they relate to peptide optimization.

  • Cross-Functional Collaboration: Collaborate effectively with chemists, biologists, and scientists from other disciplines and drug modalities in a team-oriented environment. Communicate results clearly through verbal presentations, written reports, and accurate documentation of experimental procedures. Contribute to an inclusive and supportive team culture.

  • Scientific Growth & Engagement: Demonstrate a desire to understand how bench work connects to broader drug discovery goals. Stay current with relevant literature and bring new ideas to the group. Seek out opportunities to expand technical capabilities and take on diverse scientific challenges as they arise.

MINIMUM REQUIREMENTS:

  • B.S. in chemistry or a related field with at least 5 years of experience, OR M.S. in chemistry or a related field with at least 3 years of experience.

  • A comprehensive understanding of synthetic peptide chemistry and/or organic chemistry.

  • Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.

ADDITIONAL PREFERENCES:

  • Experience with peptide synthesis instrumentation, purification, and analysis by HPLC and mass spectrometry. Skilled synthetic organic chemists with a desire to transition to peptide therapeutics are encouraged to apply.

  • Experience with bioconjugation chemistry (e.g., conjugation of small molecules, oligonucleotides, carbohydrates, fluorescent labels, and/or proteins to synthetic peptides or other modalities).

  • Familiarity with macrocyclic peptide synthesis, characterization, or optimization.

  • Familiarity with computational methods for structure-based drug design.

  • Strong communication, organizational, and interpersonal skills, with the ability to work effectively as part of diverse cross-functional teams.

  • An eagerness to present work and understand its impact on drug discovery efforts.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.


Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.

Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is

$65,250 - $169,400

Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

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About Eli Lilly

Sourced by ZipRecruiter

Eli Lilly, based in Indianapolis, IN, US, is one of the pioneers in the pharmaceutical industry with a rich history dating back to 1876. This global pharmaceutical company focuses on discovering, developing, manufacturing and selling pharmaceutical products in approximately 120 countries. The company's product categories include endocrinology, oncology, cardiovascular, neuroscience, and immunology. Having invested over $9 billion in research and development in the past decade, Eli Lilly is also committed to creating high-quality medicines that meet real needs. As a recipient of several awards and recognitions, Eli Lilly is known for its focus on life-saving research and drug development. Their mission is to make medicines that help people live longer, healthier, and more active lives.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Indianapolis, IN, US

Year founded

1876