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Project Manager Biotech Jobs in Boston, MA (NOW HIRING)

Project Manager

Boston, MA ยท On-site

$115K - $145K/yr

Summary ROLE The Project Manager (PM) is an important member of the Alira Health Clinical team. The ... biotechnology / CRO industry with 1 year of management experience TECHNICAL COMPETENCES & SOFT ...

The Project Manager II operates independently within PMO standards, defines scope and schedule, and ... Biotech, pharma, clinical, lab, or IVD experience is also acceptable. * Working knowledge of GxP ...

The Project Manager II operates independently within PMO standards, defines scope and schedule, and ... Biotech, pharma, clinical, lab, or IVD experience is also acceptable. * Working knowledge of GxP ...

The Project Manager II operates independently within PMO standards, defines scope and schedule, and ... Biotech, pharma, clinical, lab, or IVD experience is also acceptable. * Working knowledge of GxP ...

Manage overall C&Q scope, budget, schedule, resource planning, and project risks. * Serve as the ... regulated pharmaceutical, biotechnology, cell and gene therapy, or medical device projects.

^Program Project Manager - 6419102

Boston, MA ยท On-site

$70.36 - $80.36/hr

The Project Manager for the DTE Infrastructure is a role within the Technology Program Management ... Biopharmaceutical or biotechnology experience * Experience with high-growth stage companies * Agile ...

Project Manager, Connected Care

Boston, MA ยท Remote

$110K - $125K/yr

Experience working with enterprise customers within the pharmaceutical, biotech, clinical research ... Experience managing customer implementations, onboarding projects, or operational workflows for ...

Showing results 21-40

Project Manager Biotech information

See Boston, MA salary details

$23

$50

$83

How much do project manager biotech jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for project manager biotech in Boston, MA is $50.24, according to ZipRecruiter salary data. Most workers in this role earn between $43.61 and $55.10 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 Boston, MA? For Project Manager Biotech jobs in Boston, MA, the most frequently searched job titles are:
What job categories do people searching Project Manager Biotech jobs in Boston, MA look for? The top searched job categories for Project Manager Biotech jobs in Boston, MA are:
What cities near Boston, MA are hiring for Project Manager Biotech jobs? Cities near Boston, MA with the most Project Manager Biotech job openings:
Infographic showing various Project Manager Biotech job openings in Boston, MA as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $104,489 per year, or $50.2 per hour.

Project Manager

Alira Health

Boston, MA โ€ข On-site

$115K - $145K/yr

Full-time

This job post hasย expired today.ย Applications are no longer accepted.


Job description

Are you being referred to one of our roles by a connection in Alira Health? If so, please apply using the referral link emailed to you.

Join our global team dedicated to innovation and initiative, where physical walls and different time zones donโ€™t limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others.

Job Description Summary

Job Description

ROLE

The Project Manager (PM) is an important member of the Alira Health Clinical team. The PM ensures the efficient implementation of one or more study protocols, works closely with all Clinical team members, and communicates directly with study sponsors and vendors.

KEY RESPONSABILITIES
  • Manages clinical research studies to ensure studies are conducted in accordance with approved scope of work/budget, ICH GCP guidelines, and FDA regulations and within established timelines.

  • Serves as study lead and primary contact for sponsors.

  • Manages clinical study functions, which may include investigational supply, IWRS/IXRS, data management, biostatistics, pharmacovigilance, and central laboratory.

  • Generates and presents frequent study status updates and reports to sponsor.

  • Supervises and provides support to the Clinical team, including Clinical Assistants, In-house Clinical Research Associates, and Clinical Research Associates.

  • Supervises and trains Associate PMs.

  • Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/form templates, study manuals and plans, site binders, etc.

  • Drives and facilitates clinical teamwork and communications to ensure timely attainment of trial milestones.

  • Ensures accuracy of reports and material work product.

  • Provides monthly billing information to finance team.

  • Presents at project meetings such as investigator meetings and new client meetings.

  • Updates management accurately and regularly through frequent communication.

  • Identifies issues and develops problem-solving strategies to ensure study timelines are met.

  • Manages subject accrual, retention, and compliance.

  • Assists in TMF management and manages TMF reviews as needed.

  • Prepares for and participates in third-party audits and FDA inspections.

  • Complies with and ensures team compliance with ICH GCP guidelines, FDA regulations, and company SOPs.

  • Participates in internal, client/sponsor, scientific, and other meetings as required.

  • Performs additional duties as assigned.

DESIRED QUALIFICATION & EXPERIENCE
  • BS/BA from an undergraduate program (life sciences or related discipline preferred) or equivalent experience

  • 3 years of experience in the pharmaceutical / biotechnology / CRO industry with 1 year of management experience 

TECHNICAL COMPETENCES & SOFT SKILLS
  • Proven ability to be careful, thorough, and detail-oriented 

  • Strong organizational skills and the ability to multi-task and work effectively in a fast-paced environment

  • Strong analytical, negotiation, meeting management, cross-functional team, and leadership skills

  • Self-starter who thrives in a collaborative, yet less structured team environment

  • Ability to problem-solve unstructured or ambiguous challenges 

  • Strong command of English, both written and verbal 

  • Excellent communication and interpersonal skills with customer service orientation 

  • Proficient with MS Office Suite, particularly Word and Excel

Compensation: USD $115,000 - 145,000

Languages

English

Education

Bachelor of Science (BS): Biology, Bachelor of Science (BS): Life Sciences, Bachelor of Science (BS): Pharmacy

Contract Type

Regular

Salary Range


The final offer will be determined within the applicable location-specific range and will depend on the candidateโ€™s confirmed work location, relevant experience, skills, qualifications, internal equity, and role scope.