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Biopharma Consulting Jobs (NOW HIRING)

The Biopharma Account Manager position is responsible for growth and expansion of direct sales in ... Proven ability to manage complex, consultative sales cycles involving multiple stakeholders and ...

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Biopharma Consulting information

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$11K

$96.5K

$137K

How much do biopharma consulting jobs pay per year?

As of Jun 15, 2026, the average yearly pay for biopharma consulting in the United States is $96,545.00, according to ZipRecruiter salary data. Most workers in this role earn between $50,000.00 and $125,000.00 per year, depending on experience, location, and employer.

What is biopharma consulting?

Biopharma consulting is a specialized service where experts provide advice and guidance to companies in the biotechnology and pharmaceutical industries. Consultants help organizations with areas such as regulatory compliance, clinical trial design, market access, strategic planning, and product development. Their expertise helps biopharma companies navigate complex industry regulations, accelerate time to market, and optimize operations. Biopharma consultants may work independently or as part of consulting firms, supporting startups, established companies, or investors in the sector.

What is the difference between Biopharma Consulting vs Biopharma Project Manager?

AspectBiopharma ConsultingBiopharma Project Manager
Required CredentialsTypically requires a degree in life sciences, business, or related fields; often an MBA or advanced degree is preferredRequires a degree in life sciences, engineering, or related fields; PMP certification is common
Work EnvironmentConsulting firms, client sites, or remote; project-based work with multiple clientsBiopharma companies or contract organizations; focused on managing specific projects within a company
Employer & Industry UsageConsulting firms serving biopharma clients; industry-wide applicationBiopharma companies, biotech firms, or CROs; internal project management roles

In summary, Biopharma Consulting involves advising multiple clients on biopharma strategies and solutions, often requiring broader industry knowledge and flexible work settings. In contrast, a Biopharma Project Manager focuses on overseeing specific projects within a single organization, emphasizing project execution and internal coordination.

What are some common challenges faced by biopharma consultants when working with multiple clients simultaneously?

Biopharma consultants often juggle several projects at once, each with its own unique timelines, regulatory requirements, and stakeholder expectations. Balancing these demands requires strong organizational skills and the ability to quickly adapt to different company cultures and scientific focuses. Additionally, consultants must stay up-to-date with evolving industry regulations and scientific advancements to provide relevant, high-quality advice. Effective communication and proactive project management are essential to ensure that all client needs are met and deadlines are achieved.

What are the key skills and qualifications needed to thrive as a Biopharma Consultant, and why are they important?

To thrive as a Biopharma Consultant, you need expertise in life sciences or pharmaceutical sciences, industry experience, and often an advanced degree such as a PhD, PharmD, or MBA. Familiarity with regulatory frameworks (e.g., FDA, EMA), clinical trial management systems, and data analysis tools like SAS or R is crucial. Excellent communication, problem-solving, and stakeholder management skills help consultants effectively advise clients and drive project success. These skills and qualifications are essential for providing actionable guidance, ensuring regulatory compliance, and supporting innovation within biopharmaceutical organizations.
More about Biopharma Consulting jobs
What cities are hiring for Biopharma Consulting jobs? Cities with the most Biopharma Consulting job openings:
What states have the most Biopharma Consulting jobs? States with the most job openings for Biopharma Consulting jobs include:
Infographic showing various Biopharma Consulting job openings in the United States as of June 2026, with employment types broken down into 33% Full Time, 33% Temporary, and 34% Contract. Highlights an 100% In-person job distribution, with an average salary of $96,545 per year, or $46.4 per hour.
Associate Scientist, Biopharma Solid Dosage (JP9989)

Associate Scientist, Biopharma Solid Dosage (JP9989)

3 Key Consulting

Thousand Oaks, CA

Other

Posted 9 days ago


Job description

Job Title:Associate Scientist, Biopharma Solid Dosage (JP9989)
Location:Thousand Oaks, CA.
Employment Type: Contract
Business Unit:Pivotal Synthetic Drug Product group of the Drug Product Technologies (DPT)
Duration:2 years with likely extension or conversion to permanent
Posting Date:03/28/2022
3 Key Consulting is hiring anAssociate Scientistfor a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
Seeking for an enthusiastic, highly motivated, and team-oriented scientist for the position of Associate Scientist. In this role, the scientist will serve as member of Drug Product development teams, providing hands-on formulation and process expertise during the development of clinical and commercial formulations for solid oral dosage forms. The individual will design and execute formulation experiments, organize and analyze results with minimal supervision, and communicate data and interpretation to work group. In addition, this individual will ensure that contracted studies are conducted in compliance with the respective protocol and applicable guidelines and regulations.
Skills: Degree in Chemical Engineering, Chemistry, Biochemistry, Biomedical Engineering or related fields; experience in a scientific working environment.
BS and or MS in Chemistry, Chemical Engineering, Biomedical Engineering, Material Sciences, Pharmaceutical Sciences, or other relevant field
Ideal candidate will have solid oral dosage formulation experience. Someone motivated to come in and learn something new and want to be an active part of the team.
Why is the Position Open?
Supplement additional workload on team
Top Must-Have Skill Sets:
  • BS and MS in Pharmaceutical Sciences, Material Sciences, Chemistry, Chemical Engineering, or other relevant field with 2+ years of experience in pharmaceutical industry with emphasis on oral solid dosage forms.
  • Understanding of typical unit operations for the manufacture of oral solid dosage forms and experience in statistical design of experiments.
  • Knowledge and hands-on experience in material characterization such as true/envelope density measurement, particle size distribution, powder rheometer, texture analyzer, BET, etc.
Day to Day Responsibilities:
The scientist will design and execute formulation and process design experiments, organize and analyze results with minimal supervision. The experimental results will lead to the best possible formulation and processes.
Employee Value Proposition:
The person in this role will get real time exposure to new molecule entities and appreciate new knowledge gained across multiple projects.
Red Flags:
No solid dosage experience
Interview process:
Phone interview and video interview
We invite qualified candidates to sendyour resume torecruiting@3keyconsulting.com. Ifyou decide that you're not interested in pursuing this position, please feel free to look at the other positions on our websitewww.3keyconsulting.com/careers. You are welcome to also sharethis opportunity withanyone you think might be interested in applying for this role.