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Bioanalytical Project Manager Jobs in Inkster, MI

MMS Holdings Inc.

Nonclinical Writer

Canton, MI · On-site

... bioanalytical reports, clinical pathology reports, PK/TK evaluation reports) * Collaborate with cross-functional teams such as project management, safety, efficacy, biostats, regulatory operations ...

MMS

Nonclinical Writer

Canton, MI · On-site

... bioanalytical reports, clinical pathology reports, PK/TK evaluation reports) * Collaborate with cross-functional teams such as project management, safety, efficacy, biostats, regulatory operations ...

All JobsBioanalytical Project Manager JobsBioanalytical Project Manager Jobs in Inkster, MI

Bioanalytical Project Manager information

See Inkster, MI salary details

$41.6K

$90.4K

$144.6K

How much do bioanalytical project manager jobs pay per year?

As of Jun 26, 2026, the average yearly pay for bioanalytical project manager in Inkster, MI is $90,371.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,200.00 and $105,800.00 per year, depending on experience, location, and employer.

Can I make 100k as a project manager?

Bioanalytical Project Managers can earn $100,000 or more annually, especially with experience, advanced certifications, and working in the pharmaceutical or biotech industries. Salaries vary based on location, company size, and project scope, with senior roles and those managing larger teams typically earning higher compensation.

What does a Bioanalytical Project Manager do?

A Bioanalytical Project Manager oversees and coordinates bioanalytical studies, ensuring that projects are completed on time, within budget, and according to regulatory standards. They act as the main point of contact between clients, laboratory teams, and regulatory agencies, managing study timelines, resources, and data quality. Their responsibilities include planning project activities, monitoring progress, troubleshooting issues, and reporting results to stakeholders. They play a critical role in drug development by ensuring that bioanalytical testing meets scientific and compliance requirements.

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

To thrive as a Bioanalytical Project Manager, you need a strong background in bioanalysis, project management experience, and typically a degree in life sciences or a related field. Familiarity with laboratory information management systems (LIMS), regulatory guidelines (such as GLP/GCP), and project management tools like MS Project is essential. Excellent communication, leadership, and organizational skills help manage cross-functional teams and client expectations. These skills ensure the successful planning, execution, and delivery of complex bioanalytical projects within regulatory and timeline constraints.

What is the highest paying project manager job?

In the field of bioanalytical project management, senior roles such as Director of Project Management or Program Manager typically offer the highest salaries, often exceeding $120,000 annually. These positions require extensive experience, leadership skills, and often involve managing multiple projects or teams in a regulated environment.

What is the job description of a bioanalyst?

A bioanalytical project manager oversees the planning, execution, and validation of bioanalytical assays used in drug development and clinical trials. They coordinate laboratory activities, ensure compliance with regulatory standards, and manage timelines and budgets, often requiring knowledge of techniques like LC-MS/MS and relevant certifications. Strong project management and scientific expertise are essential for success in this role.

What are some common challenges faced by Bioanalytical Project Managers, and how can they be addressed?

Bioanalytical Project Managers often face challenges coordinating timelines across multiple stakeholders, such as laboratory teams, clients, and regulatory bodies. Managing shifting project priorities and ensuring data integrity under tight deadlines can also be demanding. To address these challenges, effective communication, proactive risk management, and strong organizational skills are essential. Regular status meetings, clear documentation, and building strong relationships with both internal and external partners help keep projects on track and ensure compliance with regulatory standards.

Are project managers still in demand?

Bioanalytical Project Managers are in demand due to the growth of the biotech and pharmaceutical industries, which require skilled professionals to oversee complex research projects. Strong project management skills, familiarity with regulatory requirements, and experience with laboratory tools increase employability in this field.

What is the difference between Bioanalytical Project Manager vs Bioanalytical Scientist?

AspectBioanalytical Project ManagerBioanalytical Scientist
CredentialsBachelor's or Master's in Life Sciences, PMP often preferredDegree in Biology, Chemistry, or related field; PhD or Master's common
Work EnvironmentProject teams, client meetings, coordination rolesLaboratory research, data analysis, method development
Employer & Industry UsagePharmaceutical, biotech companies, CROsResearch labs, pharmaceutical companies, CROs

The Bioanalytical Project Manager oversees project timelines, budgets, and client communication, ensuring successful completion. In contrast, the Bioanalytical Scientist focuses on experimental design, data collection, and method development. Both roles are essential in the bioanalytical industry but differ in responsibilities and daily tasks.

What job categories do people searching Bioanalytical Project Manager jobs in Inkster, MI look for? The top searched job categories for Bioanalytical Project Manager jobs in Inkster, MI are:
What cities near Inkster, MI are hiring for Bioanalytical Project Manager jobs? Cities near Inkster, MI with the most Bioanalytical Project Manager job openings:
Bioanalytical Project Manager jobs near you
Nonclinical Writer

Nonclinical Writer

MMS Holdings Inc.

Canton, MI • On-site

Full-time

Posted 26 days ago

Job description

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.
This person will participate in the development, writing, and management of highly technical nonclinical documents. This is a full-time, remote position.
Roles and Responsibilities:
  • Strong experience with development and writing of nonclinical documents (eg, Module 2.4 and 2.6 eCTD submission documents, Investigator's Brochure [IB], Nonclinical Study Reports, Meeting Requests, Briefing Documents, RTQs)
  • Lead projects independently with minimal oversight, lead the writing (structure, content and messaging) of nonclinical documents, ensure the nonclinical package aligns with current regulatory guidelines and meets scientific integrity
  • Ability to author based on highly technical sources such as GLP and non-GLP nonclinical study reports, in vivo and in vitro nonclinical data
  • Ability to develop a mapping plan for the placement of nonclinical studies within structure of Module 2.4 and 2.6 eCTD submission documents
  • Interpret and analyze applicable pharmacokinetics, pharmacology, and toxicology data (eg, Prism files, bioanalytical reports, clinical pathology reports, PK/TK evaluation reports)
  • Collaborate with cross-functional teams such as project management, safety, efficacy, biostats, regulatory operations, and CMC
  • Demonstrated ability to lead others to complete complex projects
  • Ability to complete documents according to sponsor's format, processes, and according to regulatory guidelines
  • Ability to effectively operate in an environment that requires negotiation, persuasion, collaboration, and analytical judgment
  • Organizational expert within the nonclinical subject area
  • Excellent written/oral communication and strong time and project management skills
  • Ability to attend regular team meetings, lead client meeting and CRMs
  • Ability to work in various client systems (eg, SharePoint, Veeva RIM, PleaseReview, EndNote), templates and toolbars
  • Strong understanding of regulatory guidances as it applies to nonclinical submission documents and drug development (eg, ICH, FDA and EMA regulations and guidelines, GLP, GCP, GMP and GDP)
Requirements:
  • BS + in pharmacology, toxicology, biology or chemistry, or related field, with industry experience within regulatory writing, regulatory affairs, laboratory sciences, quality assurance/control
  • Knowledge of GLP, ICH guidelines, and applicable regulatory requirements
  • 2+ years of pharmaceutical regulatory nonclinical writing experience
  • Strong writing and analytical skills
  • Proficiency with MS Office applications.
  • Hands-on experience with clinical trial and pharmaceutical development preferred
  • Basic understanding of CROs and scientific & nonclinical data/terminology, & the drug development process

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