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Remote Biotechnology Jobs in Worcester, MA (NOW HIRING)

Alloy Therapeutics

Information Security Lead

Waltham, MA · Remote

$150K - $200K/yr

Remote The Company We are Alloy Therapeutics--a biotechnology ecosystem company empowering the global scientific community to make better medicines together. Through a community of partners, we ...

Alloy Therapeutics

Information Security Lead

Waltham, MA · On-site +1

$150K - $200K/yr

Remote The Company We are Alloy Therapeutics-a biotechnology ecosystem company empowering the global scientific community to make better medicines together. Through a community of partners, we ...

Danaher

Filtration Sales Specialist

Marlborough, MA · Remote

$100K - $130K/yr

... biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're ... The position is remote and is responsible for covering the Northeast US (New England), Quebec and ...

Dyne Therapeutics

Director, Compliance

Waltham, MA · Remote

This role is based in Waltham, MA, without the possibility of being a remote role. Primary ... Experience thriving in a small, rapidly growing biotech or start-up environment with a solutions ...

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All JobsBiotechnology JobsRemote Biotechnology JobsRemote Biotechnology Jobs in Worcester, MA

Remote Biotechnology information

See Worcester, MA salary details

$27.1K

$93.5K

$184.7K

How much do remote biotechnology jobs pay per year?

As of Aug 23, 2026, the average yearly pay for remote biotechnology in Worcester, MA is $93,550.00, according to ZipRecruiter salary data. Most workers in this role earn between $55,264.00 and $121,787.00 per year, depending on experience, location, and employer.

What is a remote biotechnology?

A Remote Biotechnology job involves conducting biotechnology research, analysis, or development from a remote location instead of working in a traditional lab or office setting. These roles can include positions in bioinformatics, regulatory affairs, scientific writing, or data analysis, often leveraging cloud-based tools and virtual collaboration. Advances in technology have enabled biotech professionals to contribute to research, product development, and regulatory compliance remotely. While some hands-on lab work may require a physical presence, many tasks—such as data analysis, computational modeling, and project management—can be effectively performed from home.

What are the key skills and qualifications needed to thrive in remote biotechnology?

To thrive in a Remote Biotechnology role, you need a strong background in biological sciences, laboratory techniques, and data analysis, often supported by relevant degrees such as a B.Sc. or M.Sc. in Biotechnology or related fields. Familiarity with bioinformatics tools, cloud-based data platforms, and laboratory information management systems (LIMS) is typically required, and certifications in specialized techniques or regulatory practices can be advantageous. Excellent written and verbal communication, problem-solving skills, and self-motivation are key for effective remote collaboration and project management. These capabilities enable remote biotech professionals to drive research or product development efficiently while maintaining high standards of scientific rigor and teamwork.

What are some common challenges faced by professionals working in remote biotechnology?

Professionals in Remote Biotechnology often face challenges such as coordinating experiments and data analysis across distributed teams, managing sensitive project data securely, and maintaining clear communication without in-person interactions. Since much of the work may involve virtual collaboration and accessing remote labs or databases, learning to use specialized software and keeping up-to-date with security protocols is important. However, with strong digital skills and proactive communication, most challenges can be effectively navigated. Many employers also support remote biotech employees with virtual training, remote-access tools, and regular check-ins to ensure smooth project progress.

What are the most commonly searched types of Biotechnology jobs in Worcester, MA?

The most popular types of Biotechnology jobs in Worcester, MA are:

What job categories do people searching Remote Biotechnology jobs in Worcester, MA look for?

The top searched job categories for Remote Biotechnology jobs in Worcester, MA are:

What cities near Worcester, MA are hiring for Remote Biotechnology jobs?

Cities near Worcester, MA with the most Remote Biotechnology job openings:

Remote Biotechnology jobs near you
Infographic showing various Remote Biotechnology job openings in Worcester, MA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution, with an average salary of $93,550 per year, or $45 per hour.

Clinical Scientist, Associate Director

Candel Therapeutics

Needham, MA • On-site, Remote

$181K - $194K/yr

Full-time

Re-posted 9 days ago

Job description

Clinical Scientist, Associate Director
Remote Role: Flexible schedule with occasional travel to our Needham, MA headquarters as business needs require.
Salary: $181,000-$194,000
Why Work With Us
At Candel, our people drive our success. We value diversity, collaboration, and bold thinking in a supportive, mission-driven environment. Like a team, we show up for each other and stay focused on making a difference for patients and families. Our leadership is transparent and empowering, and our culture is built on trust, flexibility, and accountability, encouraging ownership and innovation every day.
Our Science: Advancing Cancer Immunotherapies
Candel is a clinical-stage biopharma company developing off-the-shelf, multimodal immunotherapies that stimulate personalized, systemic anti-tumor responses. Our platforms use genetically modified adenovirus and HSV constructs. With positive Phase 3 results for our lead candidate, it's an exciting time to join us and help bring transformative cancer treatments to patients. Learn more: www.candeltx.com
The Opportunity
Candel Therapeutics is seeking an experienced and intellectually curious Clinical Scientist to support our oncology clinical development programs, with an initial focus on prostate cancer and opportunities to contribute across additional solid tumor programs, including lung and brain cancer studies.
This role is ideal for someone who enjoys analyzing clinical data, asking scientific questions, solving complex problems, and working collaboratively in a lean biotech environment. You will play a key role in clinical trial execution, medical monitoring, data interpretation, regulatory documentation, and cross-functional collaboration while helping shape the future of our oncology programs.
We're looking for someone who is excited by the science, thrives in a collaborative environment, and enjoys wearing multiple hats while contributing wherever needed.
Key Responsibilities
  • Perform ongoing clinical data review and analysis to ensure data integrity, identify trends, and support safety and efficacy assessments.
  • Support medical monitoring activities, including review of adverse events, protocol deviations, eligibility assessments, and long-term safety and efficacy outcomes.
  • Author and contribute to key clinical and regulatory documents including Clinical Study Reports (CSRs), Investigator Brochures (IBs), protocols, informed consent forms (ICFs), DSURs, clinical narratives, and IND/BLA regulatory submissions.
  • Collaborate closely with Clinical Operations, Regulatory Affairs, Translational Medicine, Biostatistics, Data Management, Medical Writing, and Pharmacovigilance to deliver high-quality clinical programs.
  • Participate in the development of study synopses, protocols, statistical analysis plans, briefing books, regulatory responses, and scientific presentations.
  • Review and interpret clinical data to identify trends, investigate unexpected findings, and provide meaningful scientific insights to study teams.
  • Contribute to literature reviews, clinical evaluation reports, abstracts, manuscripts, and scientific publications.
  • Support multiple oncology programs as business priorities evolve, serving as a collaborative scientific partner across studies.
  • Help establish and continuously improve clinical development processes within a fast-growing biotechnology company.
  • Ensure compliance with ICH GCP, FDA and EMA regulations, company SOPs, and applicable industry standards.

Qualifications & Experience
  • 5+ years of Clinical Scientist or related clinical development experience within biotechnology or pharmaceutical organizations.
  • Oncology clinical development experience required; experience supporting prostate cancer, lung cancer, brain cancer, or other solid tumor studies is highly desirable.
  • Hands-on experience with clinical data review and medical monitoring.
  • Experience authoring clinical and regulatory documents including CSRs, Investigator Brochures, protocols, DSURs, IND submissions, and related regulatory documentation.
  • Experience supporting BLA preparation or regulatory filings is a plus.
  • Experience working within a small or mid-sized biotechnology company is preferred.

Core Skills & Competencies
  • Passion for oncology science with genuine curiosity about clinical data and patient outcomes.
  • Strong analytical mindset with the ability to critically evaluate clinical data, identify trends, and investigate complex scientific questions.
  • Collaborative team player who enjoys working across multiple functions in a highly interactive environment.
  • Adaptable, flexible, and comfortable supporting multiple clinical programs in a lean biotechnology company.
  • Coachable, proactive, and eager to continuously learn and expand scientific knowledge.
  • Excellent medical writing, presentation, and communication skills.
  • Strong organizational and project management skills with the ability to balance multiple priorities.
  • High attention to detail and commitment to scientific rigor, quality, and patient safety.
  • Experience with clinical trial databases, MedDRA coding, safety reporting systems, and clinical data review tools is preferred.
  • Thorough understanding of oncology clinical trial design, execution, Good Clinical Practice (ICH GCP), FDA regulations, and global clinical development.

Applicants must be legally authorized to work in the United States at the time of hire and throughout employment. We are unable to provide, assume, or sponsor employment visas now or in the future.

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