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Remote Science Jobs in Worcester, MA (NOW HIRING)

Revvity

Sr. Tax Manager (REMOTE)

Waltham, MA · On-site +1

$134K - $167K/yr

... scientists, researchers, and clinicians solve the world's greatest health challenges. We pair the enthusiasm of an industry disruptor with the experience of a longtime leader. Our team of 11,000 ...

Revvity

Sr. Tax Manager (REMOTE)

Waltham, MA · Remote

$134K - $167K/yr

... scientists, researchers, and clinicians solve the world's greatest health challenges. We pair the enthusiasm of an industry disruptor with the experience of a longtime leader. Our team of 11,000 ...

micro1 AI

AI Trainer - Microbiology Expert

Worcester, MA · Remote

$70 - $90/hr

Remote micro1 is engaging Microbiologists to contribute their scientific expertise to a unique customer project. In this role, you'll apply your expertise to help train next-generation AI systems.

Mondo

Data Product Manager

Marlborough, MA · Remote

$50 - $65/hr

Remote (Preference for candidates local to Marlborough, MA) Start Date Is: ASAP Duration: 6-month ... Partner with data engineering and data science teams to deliver scalable data solutions.

Danaher

Senior Counsel

Marlborough, MA · On-site +1

$185K - $204K/yr

Are you ready to accelerate your potential and make a real difference within life sciences ... The role is designated as fully remote ; however, there is a strong preference for the incumbent to ...

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Showing results 21-40

All JobsScience JobsRemote Science JobsRemote Science Jobs in Worcester, MA

Remote Science information

See Worcester, MA salary details

$24.4K

$48.3K

$78.8K

How much do remote science jobs pay per year?

As of Sep 5, 2026, the average yearly pay for remote science in Worcester, MA is $48,285.00, according to ZipRecruiter salary data. Most workers in this role earn between $38,400.00 and $51,900.00 per year, depending on experience, location, and employer.

What is remote science?

Remote science jobs are positions in scientific fields that can be performed outside of traditional laboratory or office environments, typically from home or any location with internet access. These jobs may include roles in research, data analysis, scientific writing, consulting, or education. Advances in technology and communication tools have made it possible for scientists to collaborate, conduct experiments, and analyze data remotely. Remote science jobs offer flexibility and can help employers and employees reach a broader talent pool. Common areas include biology, chemistry, environmental science, and healthcare research.

What skills and qualifications are needed to thrive as a remote science professional?

To thrive as a Remote Science professional, you need a strong background in your scientific discipline, analytical skills, and typically a relevant degree or higher qualification. Familiarity with data analysis tools, virtual collaboration platforms, and scientific software such as Python, R, or MATLAB is important. Excellent written communication, time management, and self-motivation are standout soft skills in this remote environment. These abilities ensure effective research, collaboration, and productivity while working independently from various locations.

What are common challenges faced by professionals working in remote science roles, and how can they be addressed?

Professionals in remote science roles often face challenges such as effective communication across time zones, limited access to lab equipment, and maintaining collaboration with team members. To address these issues, it is helpful to establish regular virtual check-ins, utilize collaborative digital tools, and set clear expectations for project milestones. Many teams also adopt cloud-based data sharing and remote access to specialized software, ensuring that scientific work continues smoothly despite physical distance.

What is the difference between Remote Science vs Remote Data Analyst?

AspectRemote ScienceRemote Data Analyst
Required CredentialsScience degrees, research experience, technical skillsStatistics, data analysis certifications, technical skills
Work EnvironmentResearch labs, academic institutions, remote research projectsBusiness, finance, tech companies, remote data analysis roles
Employer & Industry UsageUniversities, research institutes, biotech firmsCorporations, consulting firms, tech startups
Search & Comparison IntentUnderstanding research roles, scientific projectsData analysis tasks, business insights

Remote Science and Remote Data Analyst roles share a focus on technical skills and remote work environments. However, Remote Science typically involves research, scientific experiments, and academic or biotech settings, while Remote Data Analysts focus on interpreting data for business insights in corporate environments. Both roles require analytical skills but differ in industry application and specific credentials.

What remote science jobs are there?

Remote science jobs include roles such as research scientists, data analysts, laboratory technicians, and scientific writers. These positions often require specialized knowledge, relevant degrees, and skills in data analysis, laboratory techniques, or scientific software, and may involve collaboration through digital communication tools.

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

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

What are popular job titles related to Remote Science jobs in Worcester, MA?

For Remote Science jobs in Worcester, MA, the most frequently searched job titles are:

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

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

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

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

Remote Science jobs near you
Infographic showing various Remote Science job openings in Worcester, MA as of August 2026, with employment types broken down into 11% Internship, 74% Full Time, and 15% Part Time. Highlights an 100% Remote job distribution, with an average salary of $48,285 per year, or $23.2 per hour.

Clinical Scientist, Associate Director

Candel Therapeutics

Needham, MA • On-site, Remote

$181K - $194K/yr

Full-time

Re-posted 23 days ago

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.

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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