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Project Manager Biotech Jobs in Oregon (NOW HIRING)

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

You will partner with pharmaceutical and biotechnology clients to generate patient-centered ... Manage project risks, client expectations, resource allocation, and team performance. * Serve as a ...

Senior Director, Biostatistics

OR · On-site +1

$290K/yr

  • Medical

  • Retirement

  • PTO

... Project Management, Translational Medicine, and other staff and vendors to meet project ... within the pharmaceutical, biotech, or CRO industry. * Strong knowledge of statistical ...

OR · On-site

Serve as the regulatory lead on assigned R&D project teams and partner cross-functionally with ... biotech, or life sciences * 5+ years of experience in Regulatory Affairs * Strong background in ...

Senior Product Manager - Marketing

OR · On-site +1

$120K - $158K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... moving biotech environment. The right person combines strategic thinking with operational ... Strong project leadership and organizational skills with ability to manage multiple priorities ...

Strategic Account Manager

OR · On-site +1

  • Medical

  • Dental

  • Vision

  • Retirement

... Biotech and Cell & Gene industry * "Face to the customer" - centrally managing the customer ... Experience in defining and delivering IT projects in the regulated industry * Willingness to travel ...

Strategic Account Manager

OR · Remote

  • Medical

  • Dental

  • Vision

  • Retirement

... Biotech and Cell & Gene industry * "Face to the customer" - centrally managing the customer ... Experience in defining and delivering IT projects in the regulated industry * Willingness to travel ...

OR · On-site

... biotechnology industry by leading/influencing high-performing teams. With a deep understanding of ... of our key product projects, TLX250-CDx and TLX101-CDx (18F-FET) moving through the ...

Biostatistical Programming Senior Manager

OR · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

It is key to our becoming one of the world's leading biotechnology companies. We are global ... Plan and monitor progress of projects and address issues accordingly. * Support GSP Functional ...

Strategic Sourcing Manager

Portland, OR · On-site

$136K - $177K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Project Management Experience - able to lead teams that cut across geographic and functional ...

Knowledge of translational medicine and/or early discovery in the biotech or pharmaceutical industry is a plus * Excellent project management skills with a proven track record in leading successful ...

OR · On-site

Lead and influence complex projects and initiatives that impact organizational performance and ... biotechnology, healthcare, account management, sales, market access, or commercial leadership ...

Showing results 41-60

Project Manager Biotech information

See Oregon salary details

$23

$48

$80

How much do project manager biotech jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for project manager biotech in Oregon is $48.89, according to ZipRecruiter salary data. Most workers in this role earn between $42.45 and $53.61 per hour, depending on experience, location, and employer.

What is the difference between Project Manager Biotech vs Clinical Project Manager?

AspectProject Manager BiotechClinical Project Manager
CredentialsBachelor's or Master's in Life Sciences, Project Management CertificationBachelor's or Master's in Life Sciences, Clinical Research Certification
Work EnvironmentBiotech companies, R&D labs, manufacturingClinical trial sites, hospitals, pharmaceutical companies
Industry UsageBiotech product development, research projectsClinical trial management, regulatory compliance
Common Search/ComparisonYesYes

The main difference between a Project Manager Biotech and a Clinical Project Manager lies in their focus areas. The Project Manager Biotech oversees research and development projects within biotech companies, focusing on product development and manufacturing. In contrast, the Clinical Project Manager specializes in managing clinical trials, ensuring regulatory compliance and patient safety. Both roles require strong project management skills and relevant certifications, but they operate in different phases of the biotech and pharmaceutical industry.

How does a project manager in biotech typically collaborate with cross-functional teams to drive project success?

A Project Manager in the biotech sector routinely works with cross-functional teams that include scientists, regulatory experts, manufacturing staff, and quality assurance professionals. They coordinate meetings, align project timelines, and ensure clear communication of goals and milestones. Effective collaboration involves resolving conflicts, facilitating information flow among departments, and adapting plans as scientific or regulatory requirements evolve. This collaborative approach is essential for keeping projects on track, maintaining compliance, and achieving successful outcomes in a highly regulated and fast-paced industry.

What does a project manager in biotech do?

A Project Manager in Biotech is responsible for planning, coordinating, and overseeing projects within biotechnology companies or research organizations. They work closely with scientists, regulatory teams, and other stakeholders to ensure that projects meet deadlines, stay within budget, and comply with industry regulations. Their tasks may include setting project timelines, managing resources, mitigating risks, and communicating progress to leadership. Project Managers play a crucial role in bringing new biotech products or research initiatives from conception to completion.

What are the key skills and qualifications needed to thrive as a project manager in biotech?

To thrive as a Project Manager in Biotech, you need a solid background in life sciences or engineering, experience in project management, and often a relevant degree such as a BSc or MSc, sometimes complemented by a PMP certification. Familiarity with project management software (such as MS Project or Jira), regulatory compliance systems, and budgeting tools is frequently required. Strong leadership, problem-solving, and effective communication skills set standout candidates apart by enabling them to coordinate cross-functional teams and manage complex timelines. These skills are essential to ensure that projects meet regulatory standards, stay on schedule, and achieve scientific and business goals.

What are popular job titles related to Project Manager Biotech jobs in Oregon?

For Project Manager Biotech jobs in Oregon, the most frequently searched job titles are:

What cities in Oregon are hiring for Project Manager Biotech jobs?

Cities in Oregon with the most Project Manager Biotech job openings:

Infographic showing various Project Manager Biotech job openings in Oregon as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, 2% Contract, and 1% Nights. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $101,694 per year, or $48.9 per hour.

Director, Patient Centered Outcomes Assessment

RTI International

On-site

Full-time

Medical, Dental, Life, Retirement, PTO

Posted 29 days ago


RTI International rating

7.0

Company rating: 7.0 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

62nd of 73 rated research


Job description

About the Hiring Group

RTI Health Solutions (RTI-HS), a wholly owned subsidiary of RTI International, is an independent and internationally recognized research organization. With offices in the US, UK, Spain, France, and Sweden, we provide healthcare consulting and research expertise to optimize decision making for pharmaceutical, biotechnology, and medical device products across the development and marketing lifecycle. Clients rely on our expertise, quality standards, and integrity to guide their product development and regulatory and market access strategies. Our various practice areas include Value, Access, and HEOR; Patient-Centered and Outcomes Research; Epidemiology and Biostatistics; Medical Communications; Global Business Operations; and Strategic Consulting and Growth.

RTI Health Solutions is seeking an experienced and highly collaborative Senior Scientist to join our Patient-Centered Outcomes Assessment (PCOA) team. This role is ideal for a senior researcher who thrives at the intersection of hands-on execution, scientific leadership, and collaboration.

As a senior member of the PCOA team, you will lead multidisciplinary project teams while remaining actively engaged in the design, conduct, analysis, interpretation, and dissemination of patient-centered research. You will serve as both a scientific leader and a working manager-providing strategic direction, mentoring staff, and ensuring project success while directly contributing to high-impact client deliverables.

You will partner with pharmaceutical and biotechnology clients to generate patient-centered evidence throughout the drug development lifecycle, supporting regulatory, reimbursement, and market access objectives.

What You'll Do

Key Responsibilities

Project and Scientific Leadership

  • Lead complex patient-centered outcomes research programs from study design through final delivery.
  • Serve as project lead for multidisciplinary teams, ensuring projects are delivered on time, within scope, and to the highest scientific standards.
  • Provide strategic oversight of study design, methodology, regulatory engagement, and evidence generation plans.
  • Manage project risks, client expectations, resource allocation, and team performance.
  • Serve as a trusted scientific advisor to clients and internal stakeholders.

Research Execution and Technical Contribution

  • Personally contribute to the design, execution, analysis, interpretation, and reporting of qualitative and mixed-methods research studies.
  • Design and lead qualitative research conducted with patients, caregivers, patient advocates, and clinical key opinion leaders, including both stand-alone and clinical trial-based studies.
  • Lead the development, adaptation, and evaluation of clinical outcome assessments (COAs), including patient-reported outcomes (PROs), observer-reported outcomes (ObsROs), clinician-reported outcomes (ClinROs), and related measures.
  • Review and critically appraise published literature, COA development programs, and psychometric evidence.
  • Develop patient-centered evidence strategies to support regulatory, access & reimbursement, and healthcare decision-making needs.
  • Contribute directly to study reports, client presentations, evidence dossiers, briefing books, and negotiations with key decision makers to support patient-centered value messaging for medicines.

Client Leadership and Business Development

  • Build and maintain strong relationships with existing and prospective clients.
  • Lead scientific discussions with pharmaceutical and biotechnology sponsors regarding patient-focused drug development strategies.
  • Support business development efforts through proposal development, client meetings, capability presentations, and identification of growth opportunities.
  • Contribute to strategic planning and expansion of RTI-HS PCOA capabilities.

Publications, Dissemination, and Thought Leadership

  • Lead and contribute to scientific publications, conference abstracts, posters, presentations, and manuscripts.
  • Represent RTI-HS at scientific meetings, industry conferences, and client engagements.
  • Stay current with evolving regulatory guidance, methodological advancements, and industry best practices in patient-centered outcomes research.

People Leadership and Talent Development

  • Provide day-to-day leadership, mentorship, and coaching to junior and mid-level researchers.
  • Foster technical excellence, knowledge sharing, and professional development across project teams.
  • Support staff development through project leadership opportunities, scientific review, and career mentoring.
  • Contribute to building a collaborative, inclusive, and high-performing team culture.
What You'll Need
  • A postgraduate master's level degree plus a minimum of 8 years of experience conducting patient-centered research, or a PhD plus a minimum of 5 years of experience conducting patient-centered research.
  • Demonstrated experience leading complex patient-centered research projects and multidisciplinary teams within a consulting, pharmaceutical, regulatory, CRO, or academic research environment supporting patient-focused drug development.
  • Demonstrated success managing client relationships, mentoring research staff, and leading project teams.
  • Substantial experience developing and successfully executing patient-centered evidence-generation strategies for pharmaceutical clients.
  • Proven experience interacting with regulatory agencies, including FDA, EMA, or other global health authorities as well as supporting evidence needs for access stakeholders (payers HTA, and prescribers) .
  • Experience leading proposal development and contributing to business growth initiatives.
  • Strong publication record and experience presenting research at scientific conferences.

#LI-BM1

EEO & Pay Equity Statements

For San Francisco, CA USA Job Postings Only: Pursuant to the San Francisco Fair Chance Ordinance, we will consider for employment qualified applicants with arrest and conviction records. Further information is available here.

RTI accepts applications to our job openings from candidates with criminal histories or conviction records in accordance with all applicable laws, including the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.

For Applicants in Massachusetts Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

The anticipated pay range for this role is listed below. Our pay ranges represent national averages and may vary by location as a geographic differential may be applied to some locations within the United States. RTI considers multiple factors when making an offer including, for example: established salary range, internal budget, business needs, and education and years of work experience possessed by the applicant. Further, salary is merely one element to our offer.

At RTI, we demonstrate our commitment to rewarding individual and team achievement through a total rewards package. This package includes (among other things) a competitive base salary, a generous paid time off policy, merit based annual increases, bonus opportunities and a robust recognition program. Other benefits include a competitive range of insurance plans (including health, dental, life, and short-term and long-term disability), access to a retirement savings program such as a 401(k) plan, paid parental leave for all parents, financial assistance with adoption expenses or infertility treatments, financial reimbursement for education and developmental opportunities, an employee assistance program, and numerous other offerings to support a healthy work-life balance.

Hiring Salary Range$150,000.00-$250,000.00Employment Type: FULL_TIME

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