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Remote Biopharma Jobs in Seattle, WA (NOW HIRING)

The hire will report into senior leadership, represent Syner-G in the market, and shape how we show up to the West Coast biotech and biopharma community. WORK LOCATION: This position is remote with ...

Automation Sales Representative

Seattle, WA · On-site +1

$79K - $129K/yr

... Biopharma, Academia, Government and Life Sciences markets is required. * Previous exposure to ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

Redmond, WA with travel to Seattle, WA site, This role could be Hybrid or remote. Shifts: Days ... working in biopharmaceutical cGMP manufacturing preferred. * Be able to successfully work ...

Redmond, WA with travel to Seattle, WA site, This role could be Hybrid or remote. Shifts: Days ... working in biopharmaceutical cGMP manufacturing preferred. * Be able to successfully work ...

Redmond, WA with travel to Seattle, WA site, This role could be Hybrid or remote. Shifts: Days ... working in biopharmaceutical cGMP manufacturing preferred. * Be able to successfully work ...

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Remote Biopharma information

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How much do remote biopharma jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for remote biopharma in Seattle, WA is $24.47, according to ZipRecruiter salary data. Most workers in this role earn between $20.53 and $26.01 per hour, depending on experience, location, and employer.

What is a remote biopharma?

A Remote Biopharma job involves working in the biopharmaceutical industry from a remote location, rather than in a traditional office or lab setting. Roles can vary and include positions in regulatory affairs, medical writing, clinical research, sales, and project management. These jobs typically require strong communication skills, the ability to work independently, and familiarity with digital collaboration tools. Many companies in the biopharma industry offer remote opportunities to attract top talent and increase flexibility.

What skills and qualifications are needed for a remote biopharma?

To excel in a Remote Biopharma role, candidates typically need a background in life sciences, pharmaceutical industry knowledge, and experience with virtual collaboration tools. Familiarity with regulatory compliance software, electronic lab notebooks, and project management platforms like MS Teams or Asana is often required. Excellent written communication, time management, and self-motivation are invaluable soft skills in a remote setting. These strengths enable effective workflows, regulatory adherence, and successful cross-functional teamwork in the biopharma industry from a remote environment.

What are common challenges faced by professionals working remotely in the biopharmaceutical industry?

Remote biopharma professionals often encounter challenges such as maintaining clear communication across geographically dispersed teams and ensuring seamless collaboration on complex projects. Navigating data security and compliance in a virtual setting can also demand extra attention to protocol and documentation. To overcome these challenges, many teams rely on regular video meetings, digital project management tools, and robust cybersecurity practices. Working remotely, you'll need to be proactive in staying connected and informed, but many companies provide strong support networks and training to help you succeed.

What are popular job titles related to Remote Biopharma jobs in Seattle, WA?

For Remote Biopharma jobs in Seattle, WA, the most frequently searched job titles are:

What job categories do people searching Remote Biopharma jobs in Seattle, WA look for?

The top searched job categories for Remote Biopharma jobs in Seattle, WA are:

Infographic showing various Remote Biopharma job openings in Seattle, WA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution, with an average salary of $50,897 per year, or $24.5 per hour.

Senior Clinical Trial Manager

Umoja Biopharma

Seattle, WA • On-site, Remote

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 9 days ago


Job description

Umoja Biopharma is an industry-leading biotech with locations in Seattle, WA and Louisville, CO, focused on transforming the treatment of cancer with a novel integrated immunotherapy platform. Our vision is to develop off-the-shelf therapies capable of treating any tumor, any time. We are a diverse and growing team working in brand-new facilities in downtown Seattle, Washington and Louisville, Colorado, and we are looking for innovative thinkers who are excited by groundbreaking science and technology, and passionate about squaring up to the challenges inherent to cutting-edge drug development. We are committed to our core values and principles that support our overall mission and strongly invite applications from enthusiastic individuals who share our commitment and help position Umoja to deliver on our goals.  We at Umoja believe in the importance of stories; we are looking for great people to join our team to help us create more stories for ourselves, for you, and most importantly for patients and their families.

Umoja Biopharma – Your Body. Your Hope. Your Cure. 

POSITION SUMMARY

The Senior Clinical Trial Manager is primarily responsible for the operational management and oversight of Umoja's clinical studies. This individual will work closely with Clinical Operations leadership, Medical Director(s), other cross-functional team members, and designated CROs to ensure the successful completion of all clinical study activities and project deliverables within specified quality, time, and cost parameters.

The ideal candidate brings clinical operations expertise in biotech and the ability to thrive in a fast-paced, entrepreneurial environment.

This role is ideally based out of our Seattle, WA location and is onsite at least 2 days/week. We are open to remote work within the US for the right candidate.

CORE ACCOUNTABILITIES

Specific responsibilities include:  

  • Ensures studies are carried out according to the study protocol, SOPs, and ICH/GCP guidelines/regulations and study specific manuals and procedures
  • Independently develop study timelines, key deliverables, and risk/mitigation strategies
  • Lead selection and performance management of CROs and other ancillary vendors during study start-up, conduct, and close-out
  • Plan and lead study team meetings
  • Lead the development of study materials (e.g., study plans, monitoring guidelines, site initiation visit materials, site tools and worksheets)
  • Contribute to the content and review of study documents (e.g., protocol, informed consent forms, case report forms (CRF), CRF completion guidelines, product administration guidelines)
  • Track and ensure optimization of site startup activities and activation, subject enrollment, data collection, and trial closeout
  • Ensure accurate and timely execution of site visit monitoring reports
  • Identify, select, and monitor performance of sites
  • Negotiate and manage the budgets and payments for sites
  • Develop and maintain strong working relationships with study investigators and site staff
  • Manage investigational product release packages and investigational product accountability
  • Coordinate with Clinical Supply Chain Operations regarding investigational product shipment to sites
  • Oversee the Trial Master File according to ICH- GCP and SOPs
  • May assist in clinical data review and query generation
  • Collaborates closely with Clinical Operations, Clinical Development, Biometrics, Clinical Data Management, Regulatory Affairs, Translational Medicine, Clinical Supply Chain, Pharmacovigilance, and Clinical Quality Assurance
  • Actively participate in and contribute to the development of department initiatives aimed at improving efficiency and best practices

The successful candidate will have:

  • Manager Level: Bachelor's degree or equivalent in Life Sciences with at least 6 years of clinical operations experience in the pharmaceutical industry with at least 1 year experience managing industry-sponsored pharmaceutical clinical studies as a sponsor employee
  • Senior Manager Level: Bachelor's degree or equivalent in Life Sciences with at least 8 years of clinical operations experience in the pharmaceutical industry with 3+ years' experience managing industry sponsored pharmaceutical clinical trials as a sponsor employee
  • Significant knowledge of GCP/ICH guidelines and the clinical development process
  • Ability to plan, organize and conduct clinical studies with minimum oversight
  • Significant experience managing CROs and other vendors and assessing performance
  • Experience leading, managing, or mentoring clinical operational staff and cross-functional teams
  • Strong organizational skills and the ability to balance changing priorities
  • Strong interpersonal and communication (written and verbal) skills
  • Demonstrated ability to work independently and as part of a multi-functional team
  • Able to solve problems under pressure
  • Self-motivated and able to work effectively in a matrix/team environment

Preferred Qualifications:  

  • Experience supporting Phase 1 and 2 clinical trials is preferred
  • Oncology experience is highly preferred

Physical Requirements:  

  • Ability to travel as needed (approximately 20%)
  • Ability to work onsite 2 days/week at our Seattle, WA office
  • Ability to sit for prolonged periods of time

Manager Level Salary Range: $125,000 - $150,000
Senior Manager Level Salary Range: $150,000 - $175,000

Benefits Offerings

Umoja Biopharma offers its employees competitive Medical, Dental, and Vision plans. Additionally, we offer Umojians access to a 401k plan through Fidelity, with a 100% match up to their first 4% deferral. Umoja also provides a generous Paid Time Off policy, employee commuter benefits, and cell phone stipend. For a full breakdown of our benefits offerings, please see the Benefits section of our website.