172 Researchers jobs in Boston

About the Opportunity

This job description is intended to describe the general nature and level of work being performed by people assigned to this classification. It is not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of personnel so classified.

JOB SUMMARY

We are looking for a highly motivated and skilled research scientist to join our team and conduct cutting-edge research on disease dynamics and epidemiological modeling. The candidate will develop and apply mathematical and computational models to understand the transmission, evolution, and control of infectious diseases. They will collaborate with other researchers, public health agencies, and stakeholders to provide insights and guidance for disease prevention and intervention strategies. The candidate will join the Machine Intelligence Group for the Betterment of Health and the Environment (MIGHTE) led by Prof. Mauricio Santillana.

MINIMUM QUALIFICATIONS

• PhD in a quantitative field such as mathematics, statistics, physics, computer science, engineering, epidemiology, or related disciplines;
• Strong background and experience in mathematical and computational modeling of infectious disease dynamics, preferably with applications to emerging or re-emerging diseases;
• Proficiency in programming languages such as R, Python, MATLAB, C++, or similar tools for data analysis and model development;
• Experience in working with large and complex datasets from diverse sources such as surveillance systems, genomic sequences, social media, etc.;
• Excellent oral and written communication skills in English, with the ability to convey complex technical concepts to both scientific and non-scientific audiences; and
• Ability to work independently and collaboratively in a fast-paced and interdisciplinary research environment.

KEY RESPONSIBILITIES & ACCOUNTABILITIES

Research and Analysis (50%)

• Design, develop, and implement mathematical and computational models for disease transmission dynamics
• Analyze large-scale epidemiological datasets using statistical and machine learning methods
• Conduct systematic literature reviews and meta-analyses on disease dynamics topics
• Develop and validate predictive models for disease outbreak scenarios
• Perform sensitivity analyses and uncertainty quantification for model parameters
• Collaborate on multi-disciplinary research projects with epidemiologists, clinicians, and public health experts

Data Management and Computational Work (10%)

• Clean, process, and manage complex epidemiological and clinical datasets
• Develop and maintain computational pipelines for data analysis workflows
• Create reproducible research code and documentation using version control systems
• Implement quality assurance protocols for data integrity and analysis accuracy
• Maintain databases and ensure compliance with data security and privacy regulations

Scientific Communication and Dissemination (20%)

• Prepare manuscripts for publication in peer-reviewed journals
• Present research findings at national and international conferences
• Create visualizations and infographics to communicate complex results to diverse audiences
• Write technical reports and policy briefs for stakeholders and funding agencies
• Contribute to grant proposals and funding applications

Collaboration and Mentorship (10%)

• Work collaboratively with interdisciplinary research teams
• Mentor undergraduate and graduate students in research methods and analysis
• Participate in laboratory meetings, journal clubs, and departmental seminars
• Engage with external collaborators, including government agencies and international organizations
• Contribute to the development of new research initiatives and partnerships

Professional Development and Service (10%)

• Stay current with advances in disease dynamics, epidemiological methods, and computational tools
• Attend workshops, conferences, and training programs to enhance technical skills
• Participate in peer review processes for scientific journals
• Contribute to departmental and institutional service activities
• Develop independent research projects that align with laboratory and institutional goals

Position Type

Additional Information

Northeastern University considers factors such as candidate work experience, education and skills when extending an offer.

Northeastern has a comprehensive benefits package for benefit eligible employees. This includes medical, vision, dental, paid time off, tuition assistance, wellness & life, retirement- as well as commuting & transportation. Visit for more information.

All qualified applicants are encouraged to apply and will receive consideration for employment without regard to race, religion, color, national origin, age, sex, sexual orientation, disability status, or any other characteristic protected by applicable law.

Compensation Grade/Pay Type:

108S

Expected Hiring Range:

$59, $83,935.00

With the pay range(s) shown above, the starting salary will depend on several factors, which may include your education, experience, location, knowledge and expertise, and skills as well as a pay comparison to similarly-situated employees already in the role. Salary ranges are reviewed regularly and are subject to change.

Job no:

Position type: Staff Full Time

Benefit Status: Benefited-Union

Campus: UMass Lowell

Department: Electrical & Computer Eng

Salary: Anticipate salary of $55,000 - $65,000/year

Applications Open: Aug

Applications Close:

General Summary of Position:

The successful applicant will conduct analytical and experimental research in the areas of metasurfaces, antenna arrays, and help immediate supervisor in writing scholarly articles and proposals. For more information, please contact Prof. Hualiang Zhang at

The initial appointment will be for 1 year contingent upon funding, with a possibility of renewal based on productivity, successful performance and the availability of funding.

Minimum Qualifications (Required):

• PhD (or equivalent) in electrical engineering, optical engineering, physics, or closely related field
• Strong background in electromagnetics and RF/microwave engineering are highly preferred
• The ability to work effectively with diverse groups
• Familiar with optical device simulation tools (e.g. CST, HFSS, ADS)

Additional Considerations:

• Should demonstrate a minimum number of 3 publications in the field
• Experience in antennas and RF/microwave measurement
• Ability to work independently, with limited direction, as well as within a team environment
• Ability to mentor and inspire students with limited research experience

Special Instructions to Applicants:

Only current UML Employees within the Grants & Contracts (MTA/GRACE) bargaining unit will be considered during the first 10 business days of the posting. All other candidates will be considered after that period.

Initial review of applications will begin immediately and continue until position is filled. However, the position may close when an adequate number of qualified applications is received.

This position is contingent upon funding. The initial appointment will be for 1 year contingent upon productivity, successful performance and the availability of funding.

Please include a resume and cover letter with your application. Names and contact information of three references will be required during the application process.

Location

Cambridge, MA

Ref #

42959

Job Family

Research

Workplace

On-Site

Date published

11-Sep-2025

Time Type

Full time

The Zhang Lab at the Broad Institute of MIT and Harvard is looking for a full-time Research Associate with a passion for learning to join our creative, diverse, and dynamic research team. The Zhang lab is broadly focused on developing programmable therapeutics and working to improve human health and wellbeing. Examples of this work include biodiscovery efforts to discover and engineer novel biological systems for use as molecular tools, development of new modes of gene and protein delivery, and exploring ways to engineer physiology to combat disease and maintain healthy homeostasis.

This position will be focused on our engineering physiology efforts and will require extensive work with animal models (including surgeries, behavioral assays, etc). It offers an excellent opportunity to directly participate in an exciting and fast-paced field of research. The successful candidate will work closely with a small team of scientists, learning a variety of laboratory skills, including cutting-edge molecular biology techniques, cellular and immunology assays, small animal work, and rigorous data analysis. Beyond the bench, the successful candidate will also have the opportunity to develop scientific communication skills, both written and oral, and learn how to tackle complex scientific problems.

Ideal candidates demonstrate deep intellectual curiosity, have strong organizational and communication skills, work well in teams, and desire to strive for excellence. Previous experience working with mice is required.

The Zhang lab is a member of the Howard Hughes Medical Institute, the Broad Institute of MIT and Harvard, the McGovern Institute at MIT, and a part of the greater Boston life-science community including MIT and Harvard. Our lab is a fun, generous, nurturing, stimulating, fast-paced, impact-driven, and collaborative environment. We are a unique multidisciplinary lab working to bridge fundamental biology and development of biotechnology to improve human health.

The Broad Institute of MIT and Harvard offer an outstanding place to work. The workplace culture is diverse, dynamic, progressive, and supports a healthy work-life balance. To support this mission, the Zhang Lab strives for a workplace culture that supports diversity, intellectual curiosity, flexibility, and integrity. Broad employees receive a generous benefits package (including a highly competitive salary, dental, vision and health insurance, retirement plan, and additional benefits) and a range of possibilities for career advancement. Details on our benefits package can be found here.

Characteristic Duties and Responsibilities:

•Manage the Zhang lab mouse colony, including maintaining an inventory system for the lab as well as breeding and genotyping animals

•Perform routine mouse procedures, including blood collection, surgeries, and behavioral assays

•Maintain procedure room for animal work

•Design and execute research plans, analyze data, and communicate scientific results to team members at regular project update meetings

•Perform molecular biology techniques, including nucleic acid purification, molecular cloning, DNA/RNA purification, PCR, and gel electrophoresis

•Develop and execute cell-based assays to validate delivery vehicles both in vitro and in vivo

•Prepare next generation sequencing libraries and analyze the results

•Work dynamically and flexibly with team members to move projects forward, and pitch in around lab when needed

•Troubleshoot scientific problems with guidance

•Prepare, order, and maintain stocks of necessary reagents and supplies

Requirements:

•A bachelor's degree in molecular/cellular biology, neurobiology, chemistry, or a related field with lab experience

•Experience working with mice

•Ability to critically read, interpret, and adapt scientific literature

•Strong organization, documentation, and time management skills

•Ability to build excellent working relationships and foster collaboration in a team environment

Please send your resume/CV, a brief statement of interest (less than 200 words), and the contact information for at least 2 references as a single PDF to

• Manage and conduct site visits (initiation, monitoring, close-out) in accordance with the clinical trial protocol and company SOPs.
• Ensure accurate and timely data collection, source document verification, and query resolution.
• Act as the primary liaison between the investigative sites and the internal study team, fostering strong working relationships.
• Identify and report adverse events and serious adverse events promptly.
• Train and mentor junior CRAs and site staff on protocol requirements and study procedures.
• Prepare site monitoring reports and track action items to resolution.
• Contribute to the development of study documents, including protocols, case report forms (CRFs), and informed consent forms.
• Ensure compliance with all applicable regulatory requirements, including FDA, EMA, and ICH-GCP.
• Participate in investigator meetings and provide study updates.
• Assist in the review and approval of site-specific trial-related documents.

• Bachelor's degree in a life science, nursing, or related field. Advanced degree (MS, PharmD, PhD) preferred.
• Minimum of 5 years of experience as a Clinical Research Associate in the pharmaceutical or biotech industry.
• Proven experience with various therapeutic areas, with a strong understanding of drug development processes.
• Extensive knowledge of GCP, ICH, FDA regulations, and other applicable guidelines.
• Excellent communication, interpersonal, and organizational skills.
• Ability to travel up to 60% to investigative sites.
• Proficiency in electronic data capture (EDC) systems and clinical trial management systems (CTMS).
• Strong analytical and problem-solving abilities.
• Demonstrated ability to work independently and as part of a cross-functional team.

• Conduct site initiation, monitoring (routine, follow-up, and close-out), and qualification visits in accordance with GCP and company SOPs.
• Ensure accurate and timely source data verification (SDV) and review of case report forms (CRFs).
• Monitor subject safety and adherence to protocol; report adverse events and protocol deviations as required.
• Oversee site regulatory compliance, including review of essential documents and Investigator Site Files (ISF).
• Provide training and ongoing support to clinical site staff on study protocols, procedures, and regulatory requirements.
• Identify, evaluate, and recommend potential investigators and sites for clinical studies.
• Collaborate with study teams, including data management, medical monitors, and project managers, to ensure efficient trial conduct.
• Prepare monitoring reports, action items, and follow-up letters promptly.
• Participate in the development and review of study-related documents, such as protocols and monitoring plans.
• Contribute to the continuous improvement of clinical operations processes and best practices.

• Bachelor's degree in a life science, nursing, or related field; advanced degree preferred.
• Minimum of 5 years of experience as a Clinical Research Associate or in a similar clinical trial management role within the pharmaceutical or biotechnology industry.
• In-depth knowledge of ICH-GCP guidelines and other relevant regulatory requirements.
• Demonstrated experience in conducting all types of site visits and assessing site performance.
• Excellent understanding of clinical trial processes and documentation.
• Strong analytical and problem-solving skills.
• Exceptional communication, interpersonal, and organizational skills.
• Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Ability to travel to sites as required (estimated 40-60% travel).
• Commitment to ethical conduct and data integrity.

• Conducting site qualification, initiation, interim monitoring, and close-out visits in accordance with Good Clinical Practice (GCP) guidelines and protocol requirements.
• Ensuring the accuracy, completeness, and consistency of clinical trial data through source data verification and query resolution.
• Training and supporting site staff on study-specific procedures, regulatory requirements, and data collection processes.
• Monitoring investigator site compliance with all applicable regulations, SOPs, and study protocols.
• Identifying and resolving site-related issues and escalating concerns to study management as appropriate.
• Managing relationships with investigators and site personnel to foster collaboration and ensure successful trial conduct.
• Reviewing and approving essential regulatory documents submitted by trial sites.
• Participating in the development and review of clinical study protocols, case report forms (CRFs), and other study documents.
• Ensuring timely reporting of study progress, site performance, and any identified risks or issues.
• Contributing to the selection and management of clinical trial sites.
• Staying current with industry trends, regulatory changes, and best practices in clinical research.