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Remote Biotech Analyst Jobs in Michigan (NOW HIRING)

Danaher

Field Service Engineer-South East Michigan

Ypsilanti, MI · Remote

$38/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... biotechnology? At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work ... From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to more ...

Danaher

Field Service Engineer-South East Michigan

Ann Arbor, MI · Remote

$38/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... biotechnology? At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work ... From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to more ...

Danaher

Technical Applications Supervisor - Central

Detroit, MI · On-site +1

$105K - $120K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... biotechnology? At Beckman Coulter Diagnostics , one of Danaher's 15+ operating companies, our work ... From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to more ...

Danaher

Field Service Engineer-South East Michigan

Canton, MI · Remote

$38/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... biotechnology? At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work ... From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to more ...

Danaher

Field Service Engineer-South East Michigan

Detroit, MI · Remote

$38/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... biotechnology? At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work ... From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to more ...

Deloitte

System Test and Validation Lead

Detroit, MI · On-site +1

Lead CAPA activities for validation findings, including root cause analysis, effectiveness checks ... This compensation range is specific to a remote role and takes into account the wide range of ...

Deloitte

System Test and Validation Lead

Midland, MI · On-site +1

Lead CAPA activities for validation findings, including root cause analysis, effectiveness checks ... This compensation range is specific to a remote role and takes into account the wide range of ...

Deloitte

System Test and Validation Lead

Midland, MI · On-site +1

Lead CAPA activities for validation findings, including root cause analysis, effectiveness checks ... This compensation range is specific to a remote role and takes into account the wide range of ...

Deloitte

System Test and Validation Lead

Midland, MI · On-site +1

Lead CAPA activities for validation findings, including root cause analysis, effectiveness checks ... This compensation range is specific to a remote role and takes into account the wide range of ...

Deloitte

System Test and Validation Lead

Detroit, MI · On-site +1

Lead CAPA activities for validation findings, including root cause analysis, effectiveness checks ... This compensation range is specific to a remote role and takes into account the wide range of ...

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Showing results 21-40

All JobsBiotech Analyst JobsRemote Biotech Analyst JobsRemote Biotech Analyst Jobs in Michigan

Remote Biotech Analyst information

What is a remote biotech analyst?

Remote Biotech Analysts are professionals who analyze data, trends, and research in the biotechnology sector while working from a location outside of a traditional office, typically from home. They assess scientific advancements, company reports, and market developments to provide insights for investors, companies, or research institutions. Their work often involves reviewing clinical trial results, evaluating new technologies, and monitoring regulatory changes. Remote Biotech Analysts use digital communication tools to collaborate with colleagues and clients, making their expertise accessible regardless of location.

How do remote biotech analysts typically collaborate with laboratory teams and other stakeholders while working offsite?

Remote Biotech Analysts frequently use digital communication tools such as video conferencing, project management platforms, and secure data-sharing systems to stay connected with laboratory teams and other stakeholders. They participate in virtual meetings to discuss project updates, analyze data, and provide recommendations. Building strong communication habits and proactively scheduling check-ins are essential for overcoming the challenge of not being physically present. Additionally, clear documentation and timely reporting help ensure alignment and project success, making collaboration seamless despite the remote nature of the role.

What are the key skills and qualifications needed to thrive as a remote biotech analyst, and why are they important?

To thrive as a Remote Biotech Analyst, you need a strong background in biology or biotechnology, data analysis, and research methodologies, typically supported by a relevant degree. Familiarity with bioinformatics software, statistical tools like R or Python, and experience using databases such as PubMed are commonly required. Strong attention to detail, critical thinking, and effective written communication are vital soft skills for analyzing complex data and presenting findings clearly. These competencies are crucial for delivering accurate insights and supporting data-driven decisions in biotech organizations operating remotely.

What are popular job titles related to Remote Biotech Analyst jobs in Michigan?

For Remote Biotech Analyst jobs in Michigan, the most frequently searched job titles are:

What job categories do people searching Remote Biotech Analyst jobs in Michigan look for?

The top searched job categories for Remote Biotech Analyst jobs in Michigan are:

What cities in Michigan are hiring for Remote Biotech Analyst jobs?

Cities in Michigan with the most Remote Biotech Analyst job openings:

Remote Biotech Analyst jobs near you

Senior Biostatistician - Remote (US)

MMS Holdings Inc.

Canton, MI • On-site, Remote

Full-time

Re-posted 5 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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