Job Summary The Associate Director, ExploR&D Consultation Agreements is responsible for leading the ... Communicate with biotech counterparts regarding contract structure, timelines, and Lilly ...
Job Summary The Associate Director, ExploR&D Consultation Agreements is responsible for leading the ... Communicate with biotech counterparts regarding contract structure, timelines, and Lilly ...
Job Summary The Associate Director, ExploR&D Consultation Agreements is responsible for leading the ... Communicate with biotech counterparts regarding contract structure, timelines, and Lilly ...
Job Summary The Associate Director, ExploR&D Consultation Agreements is responsible for leading the ... Communicate with biotech counterparts regarding contract structure, timelines, and Lilly ...
... biotech with the global expertise and resources of a leading innovator in oncology. Our mission is ... The Associate Director, Radiopharmaceutical Manufacturing Operations will provide strategic and ...
... biotech with the global expertise and resources of a leading innovator in oncology. Our mission is ... The Associate Director, Radiopharmaceutical Manufacturing Operations will provide strategic and ...
Associate Director, Radiopharmaceutical Manufacturing Operations
Indianapolis, IN · On-site
$165 - $200/hr
... biotech with the global expertise and resources of a leading innovator in oncology. Our mission is ... Associate Director, Radiopharmaceutical Manufacturing Operations will provide strategic and ...
Associate Director, Radiopharmaceutical Manufacturing Operations
Indianapolis, IN · On-site
$165 - $200/hr
... biotech with the global expertise and resources of a leading innovator in oncology. Our mission is ... Associate Director, Radiopharmaceutical Manufacturing Operations will provide strategic and ...
... biotech with the global expertise and resources of a leading innovator in oncology. Our mission is ... The Associate Director, Radiopharmaceutical Manufacturing Operations will provide strategic and ...
... biotech with the global expertise and resources of a leading innovator in oncology. Our mission is ... The Associate Director, Radiopharmaceutical Manufacturing Operations will provide strategic and ...
... biotech with the global expertise and resources of a leading innovator in oncology. Our mission is ... The Associate Director, Radiopharmaceutical Manufacturing Operations will provide strategic and ...
... biotech with the global expertise and resources of a leading innovator in oncology. Our mission is ... The Associate Director, Radiopharmaceutical Manufacturing Operations will provide strategic and ...
As the Associate Director of Engineering, you will lead the engineering and maintenance function ... Bachelor's degree in Engineering and 8+ years of experience in pharmaceutical or biotech ...
As the Associate Director of Engineering, you will lead the engineering and maintenance function ... Bachelor's degree in Engineering and 8+ years of experience in pharmaceutical or biotech ...
Associate Director, ExploR&D Consultation Agreements
Indianapolis, IN · On-site
$132 - $194/hr
Job Summary The Associate Director, ExploR&D Consultation Agreements is responsible for leading the ... Communicate with biotech counterparts regarding contract structure, timelines, and Lilly ...
Associate Director, ExploR&D Consultation Agreements
Indianapolis, IN · On-site
$132 - $194/hr
Job Summary The Associate Director, ExploR&D Consultation Agreements is responsible for leading the ... Communicate with biotech counterparts regarding contract structure, timelines, and Lilly ...
Associate Director, Radiopharmaceutical Manufacturing Operations Indianapolis - RayzeBio - IN R16057
Indianapolis, IN · On-site
$165 - $200/hr
... biotech with the global expertise and resources of a leading innovator in oncology. Our mission is ... The Associate Director, Radiopharmaceutical Manufacturing Operations will provide strategic and ...
New
Associate Director, Radiopharmaceutical Manufacturing Operations Indianapolis - RayzeBio - IN R16057
Indianapolis, IN · On-site
$165 - $200/hr
... biotech with the global expertise and resources of a leading innovator in oncology. Our mission is ... The Associate Director, Radiopharmaceutical Manufacturing Operations will provide strategic and ...
New
Associate Director, Radiopharmaceutical Manufacturing Operations Indianapolis - RayzeBio - IN R16057
Indianapolis, IN · On-site
$165 - $200/hr
... biotech with the global expertise and resources of a leading innovator in oncology. Our mission is ... The Associate Director, Radiopharmaceutical Manufacturing Operations will provide strategic and ...
New
Associate Director, Radiopharmaceutical Manufacturing Operations Indianapolis - RayzeBio - IN R16057
Indianapolis, IN · On-site
$165 - $200/hr
... biotech with the global expertise and resources of a leading innovator in oncology. Our mission is ... The Associate Director, Radiopharmaceutical Manufacturing Operations will provide strategic and ...
New
Associate Director, Reliability Engineering
$94K - $119K/yr
... biotech companies to bring their sterile injectable products to market. With facilities in ... The Associate Director of Reliability Engineering is responsible for developing, leading, and ...
Associate Director, Reliability Engineering
$94K - $119K/yr
... biotech companies to bring their sterile injectable products to market. With facilities in ... The Associate Director of Reliability Engineering is responsible for developing, leading, and ...
We are building a new kind of biotech company, one that maintains its roots as a science-based ... The Field Based Associate Director Market Access Germany ensures alignment of local implementation ...
We are building a new kind of biotech company, one that maintains its roots as a science-based ... The Field Based Associate Director Market Access Germany ensures alignment of local implementation ...
Associate Director, Reliability Engineering
Bloomington, IN · On-site
$94K - $119K/yr
... biotech companies to bring their sterile injectable products to market. With facilities in ... The Associate Director of Reliability Engineering is responsible for developing, leading, and ...
Associate Director, Reliability Engineering
Bloomington, IN · On-site
$94K - $119K/yr
... biotech companies to bring their sterile injectable products to market. With facilities in ... The Associate Director of Reliability Engineering is responsible for developing, leading, and ...
... biotech companies to bring their sterile injectable products to market. With facilities in ... The role: The Associate Director Quality Operations is accountable for end-to-end Quality ...
... biotech companies to bring their sterile injectable products to market. With facilities in ... The role: The Associate Director Quality Operations is accountable for end-to-end Quality ...
... biotech companies to bring their sterile injectable products to market. With facilities in ... The role: The Associate Director Quality Operations is accountable for end-to-end Quality ...
... biotech companies to bring their sterile injectable products to market. With facilities in ... The role: The Associate Director Quality Operations is accountable for end-to-end Quality ...
Your Role As Associate Director, Regulatory Affairs - Biologics, you will lead regulatory strategy ... The ideal candidate brings experience in biologics, vaccines, biotechnology, or pharmaceutical ...
Your Role As Associate Director, Regulatory Affairs - Biologics, you will lead regulatory strategy ... The ideal candidate brings experience in biologics, vaccines, biotechnology, or pharmaceutical ...
Your Role As Associate Director, Regulatory Affairs - Biologics, you will lead regulatory strategy ... The ideal candidate brings experience in biologics, vaccines, biotechnology, or pharmaceutical ...
Your Role As Associate Director, Regulatory Affairs - Biologics, you will lead regulatory strategy ... The ideal candidate brings experience in biologics, vaccines, biotechnology, or pharmaceutical ...
Associate Director, RMS Quality (Small Animal and NHP)
Indianapolis, IN · On-site
$101K - $142K/yr
The Associate Director, RMS Quality (Small Animal and Non-Human Primate) provides strategic ... biotechnology, CRO, or related industries, including leadership of quality programs and teams.
Associate Director, RMS Quality (Small Animal and NHP)
Indianapolis, IN · On-site
$101K - $142K/yr
The Associate Director, RMS Quality (Small Animal and Non-Human Primate) provides strategic ... biotechnology, CRO, or related industries, including leadership of quality programs and teams.
Associate Director, Field Access Manager - Central
Indianapolis, IN · On-site
$142K - $224K/yr
The Associate Director, Field Access Management serves as the leader to a team of subject-matter ... Bachelor's Degree; 5+ years in the pharmaceutical/biotech industry. Minimum 3 years of experience ...
Associate Director, Field Access Manager - Central
Indianapolis, IN · On-site
$142K - $224K/yr
The Associate Director, Field Access Management serves as the leader to a team of subject-matter ... Bachelor's Degree; 5+ years in the pharmaceutical/biotech industry. Minimum 3 years of experience ...
$142K - $224K/yr
The Associate Director, Field Access Management serves as the leader to a team of subject-matter ... Minimum Requirements:- Bachelor's Degree; 5+ years in the pharmaceutical/biotech industry.- Minimum ...
$142K - $224K/yr
The Associate Director, Field Access Management serves as the leader to a team of subject-matter ... Minimum Requirements:- Bachelor's Degree; 5+ years in the pharmaceutical/biotech industry.- Minimum ...
Biotechnology Associate Director information
What does a biotechnology associate director do?
What are the key skills and qualifications needed to thrive as a biotechnology associate director?
What are some common challenges biotechnology associate directors face when leading cross-functional teams?
What is the difference between Biotechnology Associate Director vs Biotechnology Scientist?
| Aspect | Biotechnology Associate Director | Biotechnology Scientist |
|---|---|---|
| Required Credentials | Master's or PhD in Biotechnology, Life Sciences, or related field; extensive industry experience | Master's or PhD; focus on research and development |
| Work Environment | Leadership roles in R&D teams, project management, strategic planning | Laboratory research, experimental design, data analysis |
| Employer & Industry Usage | Biotech companies, pharmaceutical firms, biotech divisions | Research institutions, biotech companies, academia |
| Common Search & Comparison | Often compared for leadership and strategic roles | Focused on scientific research and experimentation |
The Biotechnology Associate Director typically holds a leadership position overseeing research teams and strategic projects, requiring extensive experience and advanced degrees. In contrast, a Biotechnology Scientist primarily conducts laboratory research and experiments. Both roles are vital in biotech companies, but they differ in responsibilities, focus, and career level.
What are popular job titles related to Biotechnology Associate Director jobs in Indiana?
For Biotechnology Associate Director jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Biotechnology Associate Director jobs in Indiana look for?
The top searched job categories for Biotechnology Associate Director jobs in Indiana are:
What cities in Indiana are hiring for Biotechnology Associate Director jobs?
Cities in Indiana with the most Biotechnology Associate Director job openings:

Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 12 days ago
Eli Lilly and Company rating
8.8
Based on 63 frontline employees who took The Breakroom Quiz
11th of 86 rated pharmaceutical
Job description
Organization Overview
Lilly Catalyze360 is a comprehensive approach to enabling the early-stage biotech ecosystem by democratizing access to infrastructure, expertise, and resources. Through its interconnected pillars - Lilly Ventures, Lilly Gateway Labs, Lilly ExploR&D, and Lilly TuneLab - Catalyze360 strategically removes barriers that traditionally block bold science from becoming life-changing medicines, providing biotechs with flexible combinations of capital, physical lab space, R&D capabilities, AI/ML tools, and decades of enterprise learning.
Lilly ExploR&D is a team of drug discovery and development experts who partner with biotechs from discovery through clinical proof-of-concept, putting Lilly's industry-leading capabilities behind their missions. We provide flexible support - from strategic consulting to full program execution - making it faster, easier, and more capital-efficient for innovators to transform bold science into life-changing medicines.
Job Summary
The Associate Director, ExploR&D Consultation Agreements is responsible for leading the negotiation and execution of consultation agreements between Lilly ExploR&D and external biotech partners across preclinical and development matters. This is a hands-on, high-throughput contracting role focused on drafting, redlining, and moving a large volume of consultation agreements through negotiation to signature quickly and cleanly.
Key Responsibilities
- Lead end-to-end negotiation of consultation agreements with biotech partners across preclinical and development matters, from initial term discussions through executed contract
- Move a high volume of agreements through negotiation to signature efficiently, balancing speed with rigor
- Serve as the primary interface for biotechs engaging ExploR&D through the consultation pathway, translating scientific scope into commercial terms
- Partner with ExploR&D leadership and subject-matter experts to structure consultations that align with Lilly's R&D capabilities
- Draft, redline, and finalize consultation agreements in collaboration with Legal, ensuring commercial terms, scope, and deliverables are clearly captured, and that contractual provisions reflect the risk of the scientific engagement
- Partner with Lilly scientists to translate technical scope into precise, bounded work plans, defining deliverables and responsibilities clearly
- Negotiate change orders and amendments to existing consultation agreements as scope, timelines, or deliverables evolve
- Communicate with biotech counterparts regarding contract structure, timelines, and Lilly's engagement model with clarity and credibility
- Maintain rigorous deal tracking, pipeline visibility, and cycle-time discipline across the active consultation portfolio
- Identify and drive process improvements to reduce friction, standardize terms where appropriate, and shorten time-to-signature
- Partner with Finance, Legal, and Compliance to ensure all consultations meet Lilly's governance, risk, and approval standards
- Potential to extend scope into alliance management responsibilities over time
Minimum Requirements
- Bachelor's degree in any field
- 7+ years of relevant experience in business development, contracting, or R&D consulting
- 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 Skills/Preferences
- Advanced degree in a life sciences, biomedical, or related STEM field (PhD, PharmD, MS)
- Deep R&D fluency across drug discovery and/or development, with the credibility to engage biotech scientific leaders as a peer
- Demonstrated experience negotiating agreements with external partners in biotech, pharma, or life sciences
- Direct experience drafting, redlining, and executing contracts, with strong command of terms and contract structure
- Track record of managing multiple concurrent contracts with high attention to detail and disciplined follow-through
- Experience with early-stage biotech ecosystem or external innovation
- Alliance management experience with biotech companies
- Excellent written and verbal communication, with the ability to distill complex scientific and contractual terms for varied audiences
- High comfort operating with ambiguity and building repeatable processes from the ground up
- Strong cross-functional collaboration skills across Legal, Finance, and R&D
Additional Information
- Travel up to 10% US and/or OUS
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 (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women's Initiative for Leading at Lilly (WILL).
Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is
$132,000 - $193,600
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
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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