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Pharmaceutical Development Jobs in Michigan (NOW HIRING)

Varsity Tutors

Biomedical Engineering Tutor

Kalamazoo, MI · Remote

$18 - $40/hr

Emphasizes interdisciplinary integration of engineering, biology, and medicine, connecting biomedical engineering to prosthetics, diagnostic imaging, and pharmaceutical development. * Curriculum ...

Varsity Tutors

AP Chemistry Tutor

Kalamazoo, MI · Remote

$18 - $40/hr

Emphasizes particulate-level reasoning and mathematical problem-solving, connecting chemistry to pharmaceutical development, environmental science, and materials engineering. * Curriculum Awareness ...

Varsity Tutors

AP Chemistry Tutor

Detroit, MI · Remote

$18 - $40/hr

Emphasizes particulate-level reasoning and mathematical problem-solving, connecting chemistry to pharmaceutical development, environmental science, and materials engineering. * Curriculum Awareness ...

Varsity Tutors

AP Chemistry Tutor

Ann Arbor, MI · Remote

$18 - $40/hr

Emphasizes particulate-level reasoning and mathematical problem-solving, connecting chemistry to pharmaceutical development, environmental science, and materials engineering. * Curriculum Awareness ...

Varsity Tutors

Biomedical Engineering Tutor

Detroit, MI · Remote

$18 - $40/hr

Emphasizes interdisciplinary integration of engineering, biology, and medicine, connecting biomedical engineering to prosthetics, diagnostic imaging, and pharmaceutical development. * Curriculum ...

Varsity Tutors

Biomedical Engineering Tutor

Ann Arbor, MI · Remote

$18 - $40/hr

Emphasizes interdisciplinary integration of engineering, biology, and medicine, connecting biomedical engineering to prosthetics, diagnostic imaging, and pharmaceutical development. * Curriculum ...

Violet Health PC

Partnership Development

Sylvan Lake, MI · On-site

$85 - $115/hr

Experience: 3+ years of successful experience in healthcare business development, physician liaison roles, pharmaceutical sales, or medical device sales (experience in specialty care or infusion ...

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Pharmaceutical Development information

See Michigan salary details

$20.5K

$59.6K

$114.2K

How much do pharmaceutical development jobs pay per year?

As of Aug 16, 2026, the average yearly pay for pharmaceutical development in Michigan is $59,634.00, according to ZipRecruiter salary data. Most workers in this role earn between $30,500.00 and $77,600.00 per year, depending on experience, location, and employer.

What is a pharmaceutical development?

A Pharmaceutical Development job involves researching, formulating, and optimizing new drug products to ensure safety, efficacy, and regulatory compliance. Professionals in this role work on drug formulation, process development, and scale-up for manufacturing. They collaborate with scientists, regulatory teams, and production staff to bring medications from the lab to market. This field requires strong knowledge of chemistry, biology, and regulatory requirements.

What are the key skills and qualifications needed to thrive in pharmaceutical development?

To thrive in Pharmaceutical Development, you need a strong background in pharmaceutical sciences, chemistry, or related fields, often supported by an advanced degree (MS or PhD) and experience in drug formulation and testing. Proficiency in analytical instrumentation (e.g., HPLC, GC), regulatory compliance systems, and Good Laboratory Practice (GLP) certifications are highly valued. Strong project management, problem-solving abilities, and effective communication skills set top performers apart. These competencies ensure the development of safe, effective pharmaceuticals while navigating complex regulatory requirements and cross-functional team dynamics.

What does a pharmaceutical development professional do?

Professionals in Pharmaceutical Development typically oversee the formulation and optimization of new drug products, conduct lab-based experiments, and analyze test data to ensure product efficacy and safety. They frequently collaborate with cross-functional teams such as quality assurance, regulatory affairs, and manufacturing to advance each stage of product development. Regular responsibilities also include drafting technical reports, maintaining detailed laboratory documentation, and supporting regulatory submissions. The role often requires balancing hands-on lab work with strategic planning, ensuring that all processes comply with industry standards and regulations.

What are the most commonly searched types of Pharmaceutical Development jobs in Michigan?

The most popular types of Pharmaceutical Development jobs in Michigan are:

What are popular job titles related to Pharmaceutical Development jobs in Michigan?

For Pharmaceutical Development jobs in Michigan, the most frequently searched job titles are:

What job categories do people searching Pharmaceutical Development jobs in Michigan look for?

The top searched job categories for Pharmaceutical Development jobs in Michigan are:

What cities in Michigan are hiring for Pharmaceutical Development jobs?

Cities in Michigan with the most Pharmaceutical Development job openings:

Pharmaceutical Development jobs near you
Infographic showing various Pharmaceutical Development job openings in Michigan as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 1% Temporary, and 4% Contract. Highlights an 90% Physical, 4% Hybrid, and 6% Remote job distribution, with an average salary of $59,634 per year, or $28.7 per hour.

Senior Biostatistician - Remote (US)

MMS Holdings Inc.

Canton, MI • On-site, Remote

Full-time

Re-posted 3 days ago

Job description

About MMS
Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.
Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.com or follow MMS on LinkedIn.
Senior Biostatistician:
Responsibilities:
  • Create randomization and kit schedules independently, collaborate with sponsor, randomization and drug supply management teams.
  • Develop phase 1-4 SAPs and make significant contributions to iSAPs. Create SAP TLFs shells for all phases and studies.
  • Review ADAM and TLFs; work with client and programmers to resolve comments.
  • Strong programming and logic skills (working knowledge of SAS)
  • Ability to apply drug development knowledge during production of high quality statistical analyses.
  • Perform sample size calculations for a variety of scenarios and study designs.
  • Leads projects (all phases and even a program of studies) and smaller submissions, manages client meetings, CRMs, collaborates well with regulatory, PMs and sponsor.
  • Strong knowledge of CDISC (especially SDTM and ADaM), looks to understand guidance from FDA from the different therapeutical areas.
  • Understand the various tools that we work with
  • High level knowledge of drug development as it pertains to biostatistics.
  • Provides support to Data Safety Monitoring Boards (DSMB) by preparing and presenting output as the unblinded statistician.
  • Review the statistical section of a Sponsor's protocol and ensure that the appropriate statistical methods are proposed for the study design and objectives. Provide valuable feedback to the Sponsor on the statistical aspects of the study. Create the statistical section of the Sponsor's protocol with minimal support
  • High proficiency with MS Office applications
  • Demonstrate an understanding of project management-related tasks such as timelines, scope and resource requirement estimation.
  • Provide ICH guideline based input as applicable to statistics.
  • Prepare and review statistical methods and results sections for the CSR with minimal support in collaboration with in-house medical writers.
Requirements:
  • College graduate in Biostatistics, Statistics, or Mathematics discipline or related field, masters or PhD preferred, or many years of related experience required.
  • Minimum of 5 years' experience in Biostatistics or similar field required.
  • Expert knowledge of scientific principles and concepts.
  • Has high level knowledge of drug development as it pertains to biostatistics; has the ability to apply drug development knowledge during production of high quality statistical analyses.
  • Strong SAS programming, SAS base, SAS macro experience.
  • Thorough knowledge and understanding of clinical data preferred.
  • Strong experience with data and production of TLGs.
  • Excellent scientific writing skills.
  • Strong resource for biostatistics; willing to guide others in a variety of biostatistical techniques.
  • Proficiency with MS Office applications.
  • Hands-on experience with clinical trial and pharmaceutical development preferred.
  • Good communication skills and willingness to work with others to clearly understand needs and solve problems.
  • Excellent problem-solving skills.
  • Good organizational and communication skills.
  • Familiarity with 21 CFR Part 11, FDA, and GCP requirements.
  • Basic understanding of CROs and scientific & clinical data/terminology, & the drug development process.

Please consider your application unsuccessful if we do not reach out to you within 14 days of your submission.

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