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Biotech Data Analyst Jobs in Oregon (NOW HIRING)

Avantor Inc.

Site Supervisor - Services

Aloha, OR · On-site

Ability to analyze operational data and communicate findings to non-technical audiences * Working ... Experience in pharmaceutical, biotech, or regulated manufacturing client environments * Managing ...

AMRESCO

Site Supervisor - Services

Aloha, OR

Ability to analyze operational data and communicate findings to non-technical audiences * Working ... Experience in pharmaceutical, biotech, or regulated manufacturing client environments * Managing ...

Mineralys Therapeutics

Senior Manager, FP&A

OR · On-site +1

$108K - $148K/yr

Own Adaptive Planning administration and enhancement, including model maintenance, data integrity ... Biotech, biopharmaceutical, pharmaceutical, or life sciences experience is required; commercial ...

Astrix Inc

Quality Inspector I

Clackamas, OR · On-site

$22 - $23/hr

This role also reviews documentation and analytical data for finished product release while ... MUST have Nutraceutical, food & beverage, biotech, pharma (GMP regulated industry working with raw ...

Mineralys Therapeutics

Territory Manager - Bronx, NY

OR · On-site +1

Analyze territory trends, customer needs, and competitive activity to identify opportunities and ... Execute strategic call plans by translating data and insights into impactful, customer-focused ...

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Showing results 21-40

All JobsBiotech Data Analyst JobsBiotech Data Analyst Jobs in Oregon

Biotech Data Analyst information

See Oregon salary details

$35.9K

$87.4K

$143.8K

How much do biotech data analyst jobs pay per year?

As of Sep 7, 2026, the average yearly pay for biotech data analyst in Oregon is $87,374.00, according to ZipRecruiter salary data. Most workers in this role earn between $66,100.00 and $102,600.00 per year, depending on experience, location, and employer.

What does a Biotech Data Analyst do?

A Biotech Data Analyst collects, processes, and interprets biological and clinical data to support research and decision-making in biotechnology and healthcare. They work with large datasets, applying statistical and machine learning techniques to uncover insights that drive innovation in drug development, genetics, and biomedical research. Their role often involves data visualization, database management, and collaboration with scientists and engineers. Strong analytical skills and proficiency in tools like Python, R, and SQL are essential for success in this role.

What are the key skills and qualifications needed to thrive as a Biotech Data Analyst?

To thrive as a Biotech Data Analyst, you need a strong background in biological sciences, statistics, and data analysis, often supported by a degree in bioinformatics, biotechnology, or a related field. Familiarity with software tools such as Python, R, SQL, and bioinformatics platforms, as well as experience using data visualization and statistical analysis software, is typically required. Strong attention to detail, effective communication, and problem-solving abilities set top candidates apart. These skills are essential for interpreting complex biological data, ensuring accurate results, and clearly conveying findings to research teams or stakeholders.

What are the most commonly searched types of Biotech Data Analyst jobs in Oregon?

The most popular types of Biotech Data Analyst jobs in Oregon are:

What are popular job titles related to Biotech Data Analyst jobs in Oregon?

For Biotech Data Analyst jobs in Oregon, the most frequently searched job titles are:

What job categories do people searching Biotech Data Analyst jobs in Oregon look for?

The top searched job categories for Biotech Data Analyst jobs in Oregon are:

What cities in Oregon are hiring for Biotech Data Analyst jobs?

Cities in Oregon with the most Biotech Data Analyst job openings:

Biotech Data Analyst jobs near you
Infographic showing various Biotech Data Analyst job openings in Oregon as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 14% Part Time, 3% Contract, and 1% Nights. Highlights an 86% Physical, 3% Hybrid, and 11% Remote job distribution, with an average salary of $87,374 per year, or $42 per hour.

Medical Director, Clinical Development

Kailera Therapeutics, Inc.

OR • On-site, Remote

Full-time

Posted 9 days ago

Job description

What You'll Do:

We are seeking an experienced, highly motivated Medical Director, Clinical Development to join our growing team. This individual will play a pivotal role in designing and executing clinical development programs that advance our pipeline of innovative therapeutics. The successful candidate will bring strong clinical insight, a deep understanding of drug development in a biotech setting, and a proven ability to work cross-functionally in a dynamic, fast-paced environment.

Required location: Waltham, MA (hub-based, onsite 3-4 days per week) OR Remote (home-based, onsite at a hub 1 week every other month).

Responsibilities:

  • Responsible for medical monitoring/reporting and safety activities
  • Provide medical leadership in the design, planning, and execution of clinical development strategies across multiple studies
  • Acts as the medical contact at the company for clinical/medical issues
  • Interprets, reports, and prepares oral and written results of product research, in concert with senior clinical personnel
  • Serve as the medical expert for assigned assets studies
  • Contribute to regulatory interactions and strategy, such as IND/CTA/NDA submissions and briefing packages
  • Collaborate and work closely with Clinical Operations to ensure appropriate site selection, patient recruitment strategies, and high-quality trial execution
  • Oversee and support data interpretation, analysis, and clinical study reports
  • Work closely with internal stakeholders, including Regulatory, Safety, CMC, and Translational Science teams
  • Partner with external collaborators, KOLs, CROs, and investigators
  • Support scientific publications, conference presentations, and other external communications
  • Participate in safety review meetings and provide clinical input into adverse event evaluation and reporting

Required Qualifications:

  • 2+ years of industry experience in clinical development, preferably in a biotech or small pharma environment
  • Hands-on experience designing and executing clinical trials
  • Experience with regulatory submissions and global regulatory filings
  • Understanding of GCP, clinical trial design, regulatory requirements, and safety monitoring
  • Excellent written and verbal communication skills, including protocol and regulatory document writing
  • Demonstrated ability to engage with KOLs, investigators, and cross-functional teams
  • Can work independently, self-starter attitude

Preferred Qualifications:

  • Experience across multiple therapeutic areas, including obesity, is advantageous
  • Proven track record of contributing to BLA/NDA submissions is a strong plus

Education:

  • MD or equivalent is required

Apply