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Fda Contract Jobs in Michigan (NOW HIRING)

Biostatistician

Detroit, MI · Remote

$60 - $100/hr

... experience in pharmaceutical, contract research, hospital, or academic medical contexts ... Experience preparing submission-ready deliverables for regulatory agencies (e.g., FDA, EMA) is a ...

Background screening as required by the contract. * OIG, SAM, OFAC and NSO screening. * Current ... the 3 types of FDA-approved medications to treat opiate use disorder. * 8. Must be able to ...

... the 3 types of FDA-approved medications to treat opiate use disorder. * 8. Must be able to ... Background screening as required by the contract. * OIG, SAM, OFAC and NSO screening. * Current ...

RN Corrections

Adrian, MI · On-site

$64/hr

... the 3 types of FDA-approved medications to treat opiate use disorder. * 8. Must be able to ... Background screening as required by the contract. * OIG, SAM, OFAC and NSO screening. * Current ...

Background screening as required by the contract. * OIG, SAM, OFAC and NSO screening. * Current ... the 3 types of FDA-approved medications to treat opiate use disorder. * 8. Must be able to ...

Background screening as required by the contract. * OIG, SAM, OFAC and NSO screening. * Current ... the 3 types of FDA-approved medications to treat opiate use disorder. * 8. Must be able to ...

Background screening as required by the contract. * OIG, SAM, OFAC and NSO screening. * Current ... the 3 types of FDA-approved medications to treat opiate use disorder. * 8. Must be able to ...

... the 3 types of FDA-approved medications to treat opiate use disorder. * 8. Must be able to ... Background screening as required by the contract. * OIG, SAM, OFAC and NSO screening. * Current ...

... the 3 types of FDA-approved medications to treat opiate use disorder. * 8. Must be able to ... Background screening as required by the contract. * OIG, SAM, OFAC and NSO screening. * Current ...

... the 3 types of FDA-approved medications to treat opiate use disorder. * 8. Must be able to ... Background screening as required by the contract. * OIG, SAM, OFAC and NSO screening. * Current ...

... the 3 types of FDA-approved medications to treat opiate use disorder. * 8. Must be able to ... Background screening as required by the contract. * OIG, SAM, OFAC and NSO screening. * Current ...

Background screening as required by the contract. * OIG, SAM, OFAC and NSO screening. * Current ... the 3 types of FDA-approved medications to treat opiate use disorder. * 8. Must be able to ...

... the 3 types of FDA-approved medications to treat opiate use disorder. * 8. Must be able to ... Background screening as required by the contract. * OIG, SAM, OFAC and NSO screening. * Current ...

... the 3 types of FDA-approved medications to treat opiate use disorder. * 8. Must be able to ... Background screening as required by the contract. * OIG, SAM, OFAC and NSO screening. * Current ...

Background screening as required by the contract. * OIG, SAM, OFAC and NSO screening. * Current ... the 3 types of FDA-approved medications to treat opiate use disorder. * 8. Must be able to ...

Must be supportive of the 3 types of FDA-approved medications to treat opiate use disorder. * Must ... Background screening as required by the contract. * OIG, SAM, OFAC and NSO screening. * Current ...

Background screening as required by the contract. * OIG, SAM, OFAC and NSO screening. * Current ... the 3 types of FDA-approved medications to treat opiate use disorder. * 8. Must be able to ...

Background screening as required by the contract. * OIG, SAM, OFAC and NSO screening. * Current ... the 3 types of FDA-approved medications to treat opiate use disorder. * 8. Must be able to ...

Showing results 41-60

Fda Contract information

See Michigan salary details

$35.7K

$92.4K

$121.2K

How much do fda contract jobs pay per year?

As of Aug 17, 2026, the average yearly pay for fda contract in Michigan is $92,419.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,600.00 and $103,700.00 per year, depending on experience, location, and employer.

What is an Fda contract?

An FDA Contract job refers to a temporary or project-based position working with or for the U.S. Food and Drug Administration (FDA) through a contractual agreement. These roles can be with the FDA directly or through third-party contractors supporting FDA initiatives. Responsibilities may include regulatory compliance, data analysis, scientific research, IT support, or administrative tasks. Contract positions vary in duration and benefits but provide opportunities to work in a highly regulated environment.

What are the primary responsibilities of someone working under an Fda contract?

As an FDA Contract professional, your primary responsibilities usually include developing, reviewing, and managing documents and agreements in accordance with FDA guidelines and regulations. You may coordinate closely with regulatory affairs, legal, and project management teams to ensure that all contract terms support compliance and meet project timelines. Daily tasks might involve drafting and negotiating contract language, tracking deliverables, and supporting regulatory submissions. This role is both detail-oriented and collaborative, and it provides valuable experience for those seeking advancement into regulatory management or specialist positions.

What are the key skills and qualifications needed to thrive in the Fda contract position, and why are they important?

To thrive in an FDA Contract role, you need strong knowledge of FDA regulations, compliance processes, and contract management, often supported by a background in life sciences or regulatory affairs. Familiarity with tools such as Document Control Systems, eCTD publishing software, and experience with regulatory submission platforms are typically required. Outstanding attention to detail, negotiation skills, and the ability to collaborate across cross-functional teams help candidates excel. These competencies are critical for ensuring contracts meet strict regulatory standards and for navigating the complexities of FDA approval and compliance procedures.

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

The most popular types of Fda jobs in Michigan are:

What are popular job titles related to Fda Contract jobs in Michigan?

For Fda Contract jobs in Michigan, the most frequently searched job titles are:

What cities in Michigan are hiring for Fda Contract jobs?

Cities in Michigan with the most Fda Contract job openings:

Infographic showing various Fda Contract job openings in Michigan as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 16% Part Time, 2% Temporary, 3% Contract, and 2% Nights. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $92,419 per year, or $44.4 per hour.

Biostatistician

micro1 AI

Detroit, MI • Remote

$60 - $100/hr

Part-time

Posted 11 days ago


Job description

Role Title: Biostatistician


Role Type: Contractor


Location: Remote


micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI benchmarking. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters.


Scope of Work

  1. Design and author expert-level evaluation tasks simulating real-world biostatistics challenges, such as clinical trial analysis, regulatory submission reviews, and observational study assessments.
  2. Source, construct, and curate authentic datasets including trial data, patient records, and protocol documents for task use.
  3. Define correct methodological solutions and defensible clinical interpretations for each evaluation scenario.
  4. Develop comprehensive, 35+ item rubrics to evaluate AI agent performance with respect to methodological rigor and clinical reasoning.
  5. Ensure all tasks reflect the complexity and depth of real-world biostatistics practice, avoiding simplified or textbook-style examples.
  6. Collaborate with project stakeholders to ensure deliverables align with regulatory and scientific standards.


Preferred Qualifications

  1. MS or PhD in biostatistics, statistics, or epidemiology.
  2. 4+ years of experience in pharmaceutical, contract research, hospital, or academic medical contexts.
  3. Demonstrated command of clinical study design, regulatory documentation, and observational research methodologies.
  4. Advanced proficiency in R, Python, SAS, or Stata applied to real clinical or epidemiological datasets.
  5. Strong attention to methodological detail, clinical interpretation, and regulatory sensitivity.
  6. Experience preparing submission-ready deliverables for regulatory agencies (e.g., FDA, EMA) is a plus.
  7. Excellent written communication skills and ability to author detailed grading rubrics and technical documentation.


Compensation Structure

Compensation is output-based; experts are paid per task that meets the project specifications. The time required to complete work may vary depending on the expert’s experience and workflow. Minimum submission requirements apply. Experts must submit a minimum of tasks per week.


Start Timeline & Availability

We typically fill roles within 48 hours and are looking for experts ready to jump in right away. If selected, we expect you to start your first tasks within 24–48 hours of completing onboarding.