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Consulting Services Biotech Jobs in Indiana (NOW HIRING)

... consulting services associated with operational readiness to FDA-regulated and other mission ... Experience in biotech or pharmaceutical environments preferred over medical device In-depth ...

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Consulting Services Biotech information

What are consulting services in biotech?

Consulting services in biotech refer to specialized advisory services provided to biotechnology companies or organizations. These consultants offer expertise in areas such as regulatory compliance, product development, market analysis, clinical trial management, and business strategy. Their role is to help biotech firms navigate complex scientific, regulatory, and commercial challenges, enabling them to bring products to market efficiently and successfully. Consulting services may be offered by individuals or firms with deep industry experience and technical knowledge.

What are the key skills and qualifications needed to thrive as a consulting services biotech professional?

To thrive as a Consulting Services Biotech professional, you need a solid background in life sciences or biotechnology, analytical problem-solving abilities, and typically a relevant degree such as a BS, MS, or PhD. Familiarity with industry-specific tools like data analysis software, regulatory compliance systems, and project management platforms is often required. Strong communication, client management, and adaptability are crucial soft skills for delivering tailored solutions and building client trust. These skills enable effective guidance of biotech clients through complex challenges, ensuring successful project outcomes and fostering long-term partnerships.

How does a consulting services biotech professional typically collaborate with client teams during a project?

Consulting Services Biotech professionals frequently work closely with client teams by facilitating workshops, gathering requirements, and providing expert recommendations tailored to the client's scientific and business objectives. They act as a bridge between technical experts, project managers, and stakeholders to ensure project goals are met efficiently. Regular communication, on-site visits, and progress updates are common, fostering a collaborative environment that leverages both the consulting firm's expertise and the client's in-house knowledge.

What is the difference between Consulting Services Biotech vs Biotech Research Scientist?

AspectConsulting Services BiotechBiotech Research Scientist
CredentialsTypically requires a degree in life sciences, biotech, or related fields; certifications in project management or consulting are a plusRequires a degree in biology, biochemistry, or related fields; advanced degrees like a PhD are common
Work EnvironmentPrimarily client-facing, project-based, often in offices or labs, with travel to client sitesPrimarily in research labs or academic settings, focused on experimental work and data analysis
Employer & Industry UsageConsulting firms, biotech companies, pharmaceutical firms, and contract research organizationsBiotech companies, research institutions, universities

In summary, Consulting Services Biotech professionals focus on advising and project management for biotech clients, requiring business and communication skills, while Biotech Research Scientists conduct experimental research to develop new products or understand biological processes. Both roles require strong scientific credentials but differ in work environment and career focus.

What job categories do people searching Consulting Services Biotech jobs in Indiana look for?

The top searched job categories for Consulting Services Biotech jobs in Indiana are:

What cities in Indiana are hiring for Consulting Services Biotech jobs?

Cities in Indiana with the most Consulting Services Biotech job openings:

Associate Director, ExploR&D Consultation Agreements

100 Eli Lilly and Company

Indianapolis, IN โ€ข On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post hasย expired today.ย Applications are no longer accepted.


Job description

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless workโ€”but it's work worth doing. If you're driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us. 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 โ€” Lilly Ventures, Lilly Gateway Labs, Lilly ExploR&D, and Lilly TuneLab โ€” 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 โ€” from strategic consulting to full program execution โ€” 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 Additional Information 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. #WeAreLilly At Lilly we strive to ensure our employees are part of a team that cares about them and our shared purpose of making life better for those around the world. How do we do this? We continue to look for ways to include, innovate, accelerate and deliver while maintaining integrity, excellence and respect for people. We hope that you seek to join us on our journey as we create medicine and deliver improved outcomes for patients across the globe! #WeAreLilly #J-18808-Ljbffr