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Remote Data Scientist Risk Jobs in Brighton, MA (NOW HIRING)

Axiom

Data Architect (Remote)

Boston, MA · On-site +1

$69.25 - $89/hr

Data Architect 1 - US Remote About Axiom: As the leading alternative legal services provider ... Serve as the primary data architecture liaison to the Product, Operations, and Data Science ...

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.

Wood Plc

Human Health Risk Assessor

Chelmsford, MA · On-site +1

... scientists, engineers, chemists, and database specialists. We realize that our people are what make ... Enter data into, and extract data from, standard computer programs and risk assessment spreadsheet ...

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.

Globalchannelmanagement

Remote AI Architect

Boston, MA · Remote

$90 - $92/hr

Strong understanding of data governance, privacy, security, and model risk management. * Prior ... Bachelor's degree in Computer Science, Engineering, or a related technical field. * 5+ years of ...

Synex Talent

Oncology Data Specialist

Northborough, MA · Remote

$120K - $150K/yr

... remote position. Based in Northborough, this role plays a crucial part in harnessing data to ... Associate's degree in Data Science, Health Informatics, or a related field * 1-3 years of ...

State Street Global Advisors

Market Risk

Boston, MA · On-site +1

$82K - $180K/yr

... data and risk calculations. Substantial interaction with traders and other support functions ... Hybrid remote telecommuting permitted pursuant to company policy. Minimum requirements: Master ...

IQVIA

Senior Data Team Lead (Remote)

Boston, MA · Remote

$86K - $217K/yr

This is a remote/WFH position with all necessary equipment provided. What You'll Do * Lead data ... Bachelor's degree in life sciences, health, clinical, biological, or mathematical field. * No less ...

IQVIA

Senior Data Team Lead (Remote)

Boston, MA · Remote

$86K - $217K/yr

This is a remote/WFH position with all necessary equipment provided. What You'll Do * Lead data ... Bachelor's degree in life sciences, health, clinical, biological, or mathematical field. * No less ...

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All JobsData Scientist Risk JobsRemote Data Scientist Risk JobsRemote Data Scientist Risk Jobs in Brighton, MA

Remote Data Scientist Risk information

See Brighton, MA salary details

$40.9K

$133.8K

$214.2K

How much do remote data scientist risk jobs pay per year?

As of Jul 15, 2026, the average yearly pay for remote data scientist risk in Brighton, MA is $133,764.00, according to ZipRecruiter salary data. Most workers in this role earn between $107,300.00 and $148,200.00 per year, depending on experience, location, and employer.
What are the most commonly searched types of Data Scientist Risk jobs in Brighton, MA? The most popular types of Data Scientist Risk jobs in Brighton, MA are:
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Remote Data Scientist Risk jobs near you
Infographic showing various Remote Data Scientist Risk job openings in Brighton, MA as of July 2026, with employment types broken down into 1% As Needed, 82% Full Time, 13% Part Time, and 4% Contract. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution, with an average salary of $133,764 per year, or $64.3 per hour.
Senior Safety Scientist

Senior Safety Scientist

Viridian Therapeutics, Inc.

Waltham, MA • On-site, Remote

$151K - $185K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 22 days ago

Job description

Description
At Viridian Therapeutics, we are focused on developing best-in-class medicines for people living with autoimmune and rare diseases. Leveraging our team's expertise in antibody discovery and engineering, we have created a robust pipeline of differentiated investigational therapeutic candidates for well-validated targets. Our team consists of talented, entrepreneurial-minded professionals dedicated to improving the lives of patients suffering from serious diseases. We strive for data-driven decisions, thoughtful risk-taking, and efficient use of time and funds to best position our ideas for success. We value thoughtful ideas, open communication, and transparency, and are committed to a culture that allows employees to contribute at a high level, grow their careers, and balance their personal and professional ambitions.
Reporting to the Director, Pharmacovigilance Sciences, the Senior Safety Scientist is responsible for ensuring the safety of clinical trial participants and the integrity of clinical trial data. This role involves monitoring, analyzing, and assessing adverse events and other safety data from clinical trials and other sources, to identify and validate safety signals. The Senior Safety Scientist collaborates primarily with the Product Safety Lead/Safety Physician for assigned products, and also with cross-functional team members to ensure active safety surveillance of SAEs and other clinical trial safety data and lead/assist in the preparation of safety-related documents. The Senior Safety Scientist will support the Product Safety Lead to organize and prepare for the Quarterly Safety Management Team, and other safety review meetings, as well as prepare and archive the meeting minutes. They will work with other functional groups to develop and implement risk management strategies to mitigate identified and potential risks for clinical trial participants during clinical development. They will be responsible for developing and maintaining key SOPs and controlled documents related to their scope of work.
This role may be remote or based in our Waltham, MA headquarters. Our office-based employees are required to work in the office three (3) days a week. For a remote role, travel to headquarters may be required at discretion of management.
Responsibilities (including, but not limited to):
  • Safety Data Monitoring: Continuously monitor safety data from clinical trials to identify potential safety signals
  • Safety Management Team: Organize meetings, summarize and analyze safety data and prepare meeting minutes
  • Adverse Event Reporting: Ensure the timely collection, analysis, and reporting of adverse events in accordance with regulatory requirements and company policies. Track and monitor all SAEs and SUSARs
  • Risk Management: Develop and implement risk management plans to mitigate potential safety risks
  • Regulatory Compliance: Ensure compliance with all relevant regulatory guidelines, including FDA, EMA, and ICH guidelines
  • Safety Documentation: Prepare and review safety-related documents, including Safety Management Plan, Study Protocols and Amendments, Informed Consent Forms, Investigator Brochure, DSUR/PSUR, CTD Module 2.5 & 2.7.4, Risk Management Plan and Company Core Data Sheet
  • Cross-Functional Collaboration: Work closely with clinical operations, clinical development, regulatory affairs, and other departments, including the PV vendor, to ensure the safety of clinical trial participants
  • Safety Signal Detection: Oversee the use of statistical methods and data analysis tools to detect and evaluate safety signals
  • Literature Surveillance: Oversee the PV vendor literature surveillance plan and operations
  • Training and Education: Provide training and support to clinical trial staff on safety reporting and regulatory requirements

Requirements
  • Requires a Bachelor's degree in a scientific discipline (e.g., biology, pharmacy, nursing) with 8+ years of clinical safety or pharmacovigilance
  • Advanced degree (e.g., Master's, PhD) preferred
  • Strong understanding of clinical trial processes, regulatory requirements, and safety reporting guidelines
  • Thorough knowledge of relevant EU GVP, FDA and ICH guidelines, including Good Clinical Practices (GCP) guidelines
  • Knowledge of MedDRA and WHO Drug Dictionary terminology and its application as well as experience with common safety database systems (Argus/ArisG/Veeva Safety)
  • Development and review of SOPs and Work Instructions
  • Excellent organizational skills and demonstrated ability to navigate in a fast-paced environment with changing priorities
  • Excellent verbal and written communication skills including the ability to present to both internal and external partners
  • Attention to detail and high level of accuracy
  • Ability to work both independently and as part of a team
  • Strong problem-solving skills and sound decision-making under pressure
  • The salary range for this position is commensurate with experience

Viridian offers a comprehensive benefits package including:
• Competitive pay and stock options for all employees
• Medical, dental, and vision coverage with 100% of premiums paid by Viridian for employees and their eligible dependents
• Fertility and mental health programs
• Short- and long-term disability coverage
• Life, Travel and AD&D
• 401(k) Company Match with immediate company vest
• Employee Stock Purchase plan
• Generous vacation plan and paid company holiday shutdowns
• Various mental, financial, and proactive physical health programs covered by Viridian
Viridian Therapeutics, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination, harassment, or retaliation of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by Federal, State, and Local laws. Viridian 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.
Viridian Therapeutics, Inc participates in E-Verify, the federal program for electronic verification of employment eligibility.

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