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Biotech Operations Manager Jobs in Cambridge, MA

Vrtx

Global Travel Operations, Senior Manager

Boston, MA · Hybrid

$117K - $176K/yr

Manage the day-to-day operations of the outsourced travel support model including vendor management ... Experience working in a global corporate environment within biotech or comparable regulated ...

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All JobsBiotech Operations JobsBiotech Operations Manager JobsBiotech Operations Manager Jobs in Cambridge, MA

Biotech Operations Manager information

See Cambridge, MA salary details

$33.9K

$69.4K

$129.5K

How much do biotech operations manager jobs pay per year?

As of Aug 23, 2026, the average yearly pay for biotech operations manager in Cambridge, MA is $69,356.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,800.00 and $84,700.00 per year, depending on experience, location, and employer.

What does a Biotech Operations Manager do?

A Biotech Operations Manager is responsible for overseeing the daily operations of biotechnology facilities, ensuring that production processes run efficiently and comply with industry regulations. They manage teams, coordinate schedules, oversee supply chains, and implement quality control measures. Additionally, they work closely with research and development, regulatory, and quality assurance teams to ensure products meet all safety and efficacy standards. Their role is crucial in maintaining productivity, safety, and compliance in a biotech organization.

What are the key skills and qualifications needed to thrive as a Biotech Operations Manager, and why are they important?

To thrive as a Biotech Operations Manager, you need a solid background in life sciences, business management, and regulatory compliance, often supported by a relevant degree and industry experience. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and project management tools is typically required, along with certifications like Six Sigma or PMP being advantageous. Strong leadership, problem-solving abilities, and effective communication are crucial soft skills for managing teams and cross-functional projects. These skills ensure efficient operations, regulatory adherence, and successful product delivery in the highly regulated biotech industry.

What are some common challenges faced by Biotech Operations Managers, and how can they be addressed?

Biotech Operations Managers often face challenges such as maintaining regulatory compliance, managing cross-functional teams, and ensuring smooth production processes. These challenges can be addressed by staying updated on industry regulations, fostering clear communication between departments, and implementing robust quality control systems. Additionally, leveraging project management tools and continuous process improvement strategies can help streamline operations and minimize risks.

What is the difference between Biotech Operations Manager vs Biotech Laboratory Supervisor?

AspectBiotech Operations ManagerBiotech Laboratory Supervisor
CredentialsBachelor's or Master's in Life Sciences, Business, or related fields; experience in biotech operationsBachelor's or Master's in Life Sciences; laboratory management experience; relevant certifications often preferred
Work EnvironmentOversees multiple departments, manages projects, and ensures compliance across operationsManages daily lab activities, supervises lab staff, and maintains lab safety and procedures
Employer & Industry UsageUsed in biotech companies for operational oversightCommon in research labs, biotech firms, and pharmaceutical companies for lab management

The Biotech Operations Manager focuses on overseeing overall biotech operations, including project management and compliance, while the Biotech Laboratory Supervisor concentrates on managing daily lab activities and staff. Both roles require relevant scientific credentials, but their scope and responsibilities differ significantly.

What job categories do people searching Biotech Operations Manager jobs in Cambridge, MA look for?

The top searched job categories for Biotech Operations Manager jobs in Cambridge, MA are:

What cities near Cambridge, MA are hiring for Biotech Operations Manager jobs?

Cities near Cambridge, MA with the most Biotech Operations Manager job openings:

Biotech Operations Manager jobs near you
Infographic showing various Biotech Operations Manager job openings in Cambridge, MA as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 9% Part Time, 1% Temporary, 12% Contract, and 1% Nights. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $69,356 per year, or $33.3 per hour.

Clinical Operations Senior Manager

Kiniksa Pharmaceuticals

Lexington, MA • On-site

$170K - $190K/yr

Full-time

Re-posted yesterday

Job description

Kiniksa Pharmaceuticals is a commercial-stage biopharmaceutical company developing and commercializing novel therapies for diseases with unmet need, with a focus on cardiovascular indications. With deep expertise in immunology and inflammation, Kiniksa is advancing a growing portfolio of approved and investigational medicines, anchored by its lead product, ARCALYST®, the first and only FDA-approved therapy for recurrent pericarditis. Grounded in rigorous science and bold innovation, the company fosters a highly collaborative, patient-first culture led by accomplished life sciences leaders. At Kiniksa, talented individuals are trusted and empowered to make a real impact-shaping the future of medicine while improving the lives of patients who need it most.
This is an exciting time to join Kiniksa as the company continues on a strong growth trajectory. You will join a dynamic Clinical Operations team working in a fast-paced, highly collaborative environment, with the opportunity to help shape how we deliver high-quality clinical programs and contribute to the future success of the organization.
The Senior Manager, Clinical Operations provides / supports the operational leadership and strategic oversight of the planning, conduct, and delivery of global clinical trials. This role partners cross-functionally and with external service providers to ensure studies are executed in accordance with quality, timeline, budget, and regulatory expectations.
This role is based in our Lexington, MA office and requires employees to be onsite five days per week.
Responsibilities (including, but not limited to):
  • Provide operational oversight and leadership for assigned clinical development activities.
  • Partner with cross-functional stakeholders to support effective study planning, execution, and decision-making.
  • Drive proactive identification, assessment, and escalation of operational risks and issues.
  • Oversee vendors to ensure quality delivery and performance against study objectives.
  • Support development, maintenance, and execution of study operational plans and associated deliverables.
  • Ensure implementation of protocol amendments, study changes, and operational processes in alignment with program objectives.
  • Maintain inspection readiness and support compliance with GCP, regulatory requirements, and company procedures.
  • Communicate study and program status, risks, and key metrics to stakeholders and senior management.
  • Contribute to continuous improvement initiatives that enhance clinical trial execution and operational effectiveness.

Standout Skills:
  • Strong knowledge of ICH-GCP and international clinical trial regulations.
  • Understanding of clinical trial planning, execution, risk management, and vendor oversight.
  • Ability to operate well in complex matrix environment and vendor setup and lead without authority.
  • Strong organizational, communication, and stakeholder management skills.
  • Ability to manage multiple priorities in a dynamic and ambiguous environment.
  • Demonstrated problem-solving and decision-making abilities.
  • Technical understanding of clinical trial systems and integrations.

Qualifications and Experience:
  • Bachelor's degree in a scientific, healthcare, or related field required.
  • Advanced degree preferred.
  • 7+ years of clinical operations experience within a biotechnology, pharmaceutical, or CRO environment.
  • Experience supporting and/or leading global Phase 1, 2, and/or 3 clinical trials.
  • Demonstrated experience managing CROs and external vendors.
  • Experience working within cross-functional clinical development teams.
  • Proficient with Microsoft Office and clinical systems (eTMF, CTMS, IRT, EDC).

Compensation decisions are based on objective criteria including role responsibilities, experience/qualifications, internal equity, geographic location, and external market benchmarks.
Pay Range
$170,000-$190,000 USD
Kiniksa is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, transgender status, age, genetics, national origin, protected veteran status, or disability status, or any other legally protected category. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
Kiniksa does not accept unsolicited resumes from staffing agencies or search firms. Any resumes submitted without a signed agreement will be considered property of Kiniksa, and no fees will be paid.

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