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Development Scientist Jobs in Boston, MA (NOW HIRING)

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Development Scientist information

See Boston, MA salary details

$22

$42

$66

How much do development scientist jobs pay per hour?

As of Jul 27, 2026, the average hourly pay for development scientist in Boston, MA is $42.00, according to ZipRecruiter salary data. Most workers in this role earn between $30.82 and $50.14 per hour, depending on experience, location, and employer.

Do I need a PhD to be a research scientist?

A Development Scientist typically does not require a PhD; many roles accept a bachelor's or master's degree in a relevant field such as chemistry, biology, or engineering. However, a PhD can be advantageous for advanced research positions or specialized roles that involve independent project management and deep expertise.

What is the highest paid scientist job?

The highest paid scientist roles are often in executive or specialized fields such as pharmaceutical research directors, biotechnology executives, or senior data scientists in tech companies, with salaries exceeding $150,000 annually. These positions typically require advanced degrees, extensive experience, and leadership skills, and may include bonuses and stock options that significantly increase total compensation.

How to become a development scientist?

To become a development scientist, typically a bachelor's degree in a relevant field such as chemistry, biology, or engineering is required, often followed by a master's or Ph.D. for advanced roles. Gaining experience through internships, developing skills in laboratory techniques, data analysis, and familiarity with industry tools are important steps in the career path.

What is a Development Scientist?

A Development Scientist is a professional responsible for designing, developing, and optimizing products or processes, often in industries like pharmaceuticals, biotechnology, or food science. They work to improve existing technologies or create new ones by conducting experiments, analyzing data, and collaborating with cross-functional teams. Their role typically bridges the gap between research and commercial production, ensuring products are safe, effective, and scalable for market use.

How does a Development Scientist typically collaborate with cross-functional teams during a product development cycle?

Development Scientists work closely with cross-functional teams, including engineers, quality assurance, regulatory affairs, and manufacturing, throughout the product development cycle. They often lead experimental design, interpret data, and communicate findings to ensure product specifications and regulatory requirements are met. Collaboration is essential, as input from various departments is needed to troubleshoot challenges, optimize processes, and ensure a smooth transition from research to large-scale production. Effective communication, adaptability, and teamwork are key to success in this role.

What is the difference between Development Scientist vs Research Scientist?

AspectDevelopment ScientistResearch Scientist
Required CredentialsBachelor's or Master's in Chemistry, Biology, or related fieldsBachelor's, Master's, or Ph.D. in relevant sciences
Work EnvironmentProduct development labs, manufacturing settingsResearch labs, academic institutions
Employer & Industry UsagePharmaceutical, biotech, consumer goods companiesUniversities, research institutes, R&D departments

Development Scientists focus on creating and improving products, working closely with manufacturing. Research Scientists primarily conduct experiments to generate new knowledge, often in academic or research settings. While both roles require scientific credentials, Development Scientists typically work in applied settings with product goals, whereas Research Scientists focus on fundamental research. Understanding these differences helps job seekers target the right roles based on their skills and career interests.

What does a development scientist do?

A development scientist researches and develops new products, processes, or technologies in fields such as pharmaceuticals, chemicals, or consumer goods. They design experiments, analyze data, and collaborate with teams to improve or create innovative solutions, often using laboratory equipment and scientific methods.

What are the key skills and qualifications needed to thrive as a Development Scientist, and why are they important?

To thrive as a Development Scientist, you need a strong background in life sciences or chemistry, typically with a relevant degree (such as a BSc, MSc, or PhD), and experience in experimental design and data analysis. Familiarity with laboratory instrumentation, analytical software (like HPLC or GC), and adherence to regulatory standards such as GMP or GLP are crucial. Strong problem-solving skills, attention to detail, and effective communication make candidates stand out in this role. These skills and qualities ensure reliable scientific results, successful product development, and compliance with industry regulations.
Development Scientist jobs near you
Infographic showing various Development Scientist job openings in Boston, MA as of July 2026, with employment types broken down into 1% As Needed, 79% Full Time, 18% Part Time, and 2% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $87,368 per year, or $42 per hour.
Clinical Development Scientist

Clinical Development Scientist

Viridian Therapeutics, Inc.

Waltham, MA • On-site

$127K - $155K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 21 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.
Reporting to the VP of Clinical Development, the Clinical Development Scientist will support all aspects of clinical development (safety, science, and operations), including the safety and pharmacovigilance team and trial activities. Additionally, the Clinical Development Scientist will author and review key trial data-related documents and be responsible for the life cycle management of these documents.
This role may be based in Waltham, MA, which would be a hybrid role, or it can also be fully remote. Our office-based employees are required to work in the office three (3) days a week. If remote, travel to headquarters for meetings would be required at the discretion of management.
Responsibilities (including, but not limited to):
  • Contribute to the development of clinical trial strategies and study design and work with the VP of Clinical Development in study protocol development, Investigator's Brochure updates, procedure manual development, Clinical Study Report development and scientific strategy
  • Support the VP of Clinical Development in collaborating with clinical leadership and cross-functional study teams to plan and execute clinical trials, with scientific integrity, from protocol concept through the clinical study report
  • Collaborate closely with Clinical Operations colleagues on clinical trial activities and timelines, including Informed consent development and review, data management activities and review of data management plans and other documents, and management of clinical development document deliverables to meet the operational needs of the program
  • Support Clinical Development in the activities associated with execution of clinical trials and data collection, including training of the internal team, vendors, and site staff; preparation of case report forms; identification and prevention of protocol deviations; and resolution of issues
  • Collaborate closely with Safety/Pharmacovigilance colleagues on clinical trial activities and timelines, including monitoring data to characterize safety information, in collaboration with the Medical Monitor and management of safety communications with clinical investigators
  • Contribute to overall clinical data review including data listings review to detect data trends and ensure data quality and coordinate these activities with cross-functional teams and engaged vendors
  • Responsible for the management of Data Safety Monitoring Board (DSMB) activities including collection of required qualification documents, development of DSMB Charters, coordinating DSMB meetings (scheduling, preparing materials and meeting minute responsibilities)
  • Support the interface with preclinical research and clinical development in the evaluation of scientific communication opportunities and management of the review and submission process
  • Partner with Viridian safety/PV and regulatory and the safety management vendor for worldwide safety reporting
  • Contribute to the preparation of clinical sections of regulatory documents (INDs); prepare for meetings with FDA/EMA
  • Stay current with GCP and worldwide regulatory requirements

Qualifications:
  • Requires a Bachelor's degree in Life Sciences and 5+ years' experience or Master's degree with 4+ years' experience or PhD with 2+ years' experience (or commensurate with other relevant Life Sciences degree)
  • Requires relevant experience in the biotechnology or pharmaceutical industry
  • Clinical experience across all phases of therapeutic development for multiple indications, with 2+ years in Clinical Development
  • Therapeutic area experience in Ophthalmology is strongly preferred; experience in Immunology or Neurology is a plus
  • Proven success record in the execution of clinical development strategies, as well as the successful submission of IND's
  • Experience authoring clinical documents eg, clinical protocols/ synopses, Investigator Brochures'; conducting literature reviews
  • Experience supporting drug safety and pharmacovigilance activities
  • Thorough knowledge of FDA regulatory requirements, clinical research concepts & practices, and ICH/GCP guidelines
  • Experience working with and managing third party vendors, such as CRO's
  • Proven ability for strategic thinking, creative problem-solving, and risk identification & mitigation skills
  • Team-oriented and works collaboratively as a team
  • Demonstrated strong written and verbal communication skills
  • Proven mindset of proactive continuous improvement
  • Efficient independent worker with ability to focus and drive for results
  • Strong attention to detail
  • Ability to work in a fast paced-environment and to handle multiple tasks
  • Strong commitment to ethical standards
  • Proficient with Microsoft Office suite (i.e., Word, PowerPoint, Excel, Outlook, SharePoint, etc.)
  • Ability to travel up to 10-20% domestic and internationally
  • 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 insurance
  • 100% Paid Parental Leave
  • 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 fertility, mental, financial, and proactive physical health programs

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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