20 Best Scientist jobs in Cambridge, MA (Hiring Now!)

Site Manager-Dorchester, MA
Care Access —Dorchester, MA
Act as a primary point of contact in the therapeutic field for Care Access Research. Ability and willingness to mentor and guide less experienced CRC as they…
Estimated: $89.2K - $113K a year
Quick Apply
Research Scientist, Integrated Pharmacology (Contract)
Vertex Pharmaceuticals —Boston, MA
Propose and develop innovative approaches to small molecule discovery based on the latest technologies and publications in the field.
$47 - $50 an hour
Research Coordinator-Brazelton Touchpoints
Boston Children's Hospital —Boston, MA
Education in child development, psychology, early childhood education or related field. Keep abreast of trends & developments in the field.
Analytical Chemist (Contract)
Vertex Pharmaceuticals —Boston, MA
The role of the Analytical Chemist contractor position will be a combination of hands-on method optimization and data review.
$45 - $48 an hour
Customer Service Technician
Reiser —Canton, MA
Participate in meetings and conference calls with sales staff and customers. Bachelor’s degree in food science or technical and or equivalent work experience.
From $25 an hour
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1d
Medical Technologist II, Blood Bank, 40 hrs Nights
Boston Medical Center —Boston, MA
Requires a Bachelor's degree from an accredited university or college in Medical Technology or Clinical Laboratory Science which includes successful completion…
Estimated: $46.1K - $58.3K a year
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Scientist
Acrivon Therapeutics —Watertown, MA
Demonstrated hands-on experience with mid to high-throughput plate-based assays including target engagement, cell viability, and cell death assays (e.g., ADP…
Estimated: $100K - $127K a year
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Quality Control Senior Associate (Contract) 22321
Vertex Pharmaceuticals —Boston, MA
Performs technical reviews of raw data. A minimum of a Bachelor's Degree in science (Biology) or related discipline is required.
$30 - $35 an hour
Scientist I
Codetru —Boston, MA
Experience with bulk RNA-seq or single cell sequencing library preparation *Demonstrated ability to perform accurate data analysis and carefully maintain a…
$25 - $27 an hour
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23h
Research Assistant III - Carmargo Lab
Boston Children's Hospital —Boston, MA
Boston Children’s Hospital offers competitive compensation and unmatched benefits including flexible schedules, affordable health, vision and dental insurance,…
Antibody Discovery- In Vitro, Director, Global Biologics
Takeda Pharmaceutical —Boston, MA
Excellent knowledge of data analysis tools to ensure thorough evaluation of datasets and information based next step decisions.
$169,400 - $266,200 a year
Cell Therapy Manufacturing Lead
Harba Solutions —Cambridge, MA
Bachelor’s Degree in Life Sciences or a related field with 2-4+ years of experience in a regulated environment. Maintain audit readiness in operations.
$28 - $29 an hour
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7d
Scientist, Protein/Antibody Purification & Analytics
Pinetree Therapeutics —Cambridge, MA
Master Degree with 3-5 years postgraduate or Ph.D. with 0-3 years postgraduate of hands-on experience with protein and/or antibody analysis, purification,…
Estimated: $86.3K - $109K a year
Quick Apply
2d
Principal Analyst - Trade, Research & Monitoring, Fidelity Digital Assets℠
Fidelity Investments —Boston, MA
You’ll be helping identify and document requirements, work with user design, legal and compliance as well as multiple technical and business partners to ensure…
Estimated: $76.7K - $97.2K a year
3d
Principal Engineer, Hydrogeologist, or Geologist
Integral Consulting Inc. —United States
M.S. or Ph.D. in civil or environmental engineering, hydrogeology, geology, or related field. Candidates should hold an advanced degree in engineering,…
$160,000 - $200,000 a year
Analytical Development Principal Research Scientist - Cell & Gene Therapy
Vertex Pharmaceuticals —Boston, MA
The individual in this role will collaborate closely with research, process development, manufacturing, regulatory and quality to develop and innovate Vertex…
Estimated: $151K - $191K a year
Scientist
Pfizer —Andover, MA
As needed, participate in the design, development and implementation of cell-based, PCR and other bioanaytical assays to meet the needs of the portfolio.
$74,900 - $124,800 a year
1d
Forensic Scientist I - Toxicology
Department of State Police —Maynard, MA
Calibrate laboratory equipment by following documented procedures and laboratory protocols, ensuring that equipment is functioning within the operating…
$64,517.96 - $93,926.30 a year
Lab Technician, Chryso, Wilmington - Construction Chemicals
Saint Gobain —Wilmington, MA
Associates degree in engineering, technical or science related field. The Lab Technician role is responsible for assignments related to the day to day…
Quick Apply
1d
Scientist, Immuno-Oncology
Merck KGaA —Billerica, MA
In addition, the candidate will be expected to develop, evaluate, and implement well-controlled in vitro experiments to interrogate target biology, and generate…
7h

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Site Manager-Dorchester, MA

Care Access - Dorchester, MA

Quick Apply

Job Details

Full-time Estimated: $89.2K - $113K a year

Benefits

Health savings account
Disability insurance
Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance
Life insurance

Qualifications

Microsoft Word
Microsoft Excel
Clinical research
LVN
RN License
Phlebotomy
5 years
Writing skills
Research
IVR
Bachelor's degree
Clinical trials
Good Clinical Practice
Computer skills
LPN
Leadership
Communication skills
FDA regulations

Full Job Description

What We Do

Care Access is delivering the future of medicine today! Care Access has a revolutionary model that breaks down traditional barriers to clinical trials that limit participation among physicians and patients to 3%. By removing this bottleneck, Care Access is helping accelerate the approval and delivery of critical and life-saving therapies.

Who We Are

We care. Our people are the engines behind our mission: to revolutionize access to clinical trials for the benefit of patients everywhere. We care for one another, find new ideas to accelerate medicine, and seed a long-term impact for generations.

Position Overview

The Site Manager is responsible for the most pivotal and complex protocols and study designs being conducted at Care Access Research sites.

What You'll Be Working On

Duties include but not limited to:

Site Support Responsibilities:

Supports Key Sponsors and CROs
Manages some of the sites most challenging therapeutic areas and study designs
Able to monitor and mentor all levels of CRCs to ensure complete understanding of Care Access Research processes, SOPs and values, ensuring that a successful transition to more demanding opportunities and responsibilities
Assist Region Manager
Assist Region Manager in performing quality control check of all study source documents for completeness and quality

Therapeutic Responsibilities:

Demonstrate deep knowledge about the therapeutic area of responsibility
Demonstrate comprehensive understanding of related Protocol designs, outcomes and timelines
Engage in continuous independent learning within the therapeutic area of responsibility
Act as a primary point of contact in the therapeutic field for Care Access Research

Study Preparation:

Study Management:
Prioritize activities with specific regard to protocol timelines
Maintain adherence to FDA regulations and ICH guidelines in all aspects of conducting clinical trials.
Maintain effective relationships with study participants and other care Access Research personnel.
Interact in a positive, professional manner with patients, sponsor representatives, investigators and Care Access Research personnel and management.
Communicate clearly verbally and in writing.

Patient Coordination:
Prescreen study candidates
Obtain informed consent per Care Access Research SOP .
Complete visit procedures in accordance with protocol.
Train others and complete basic clinical procedures, such as blood draws, vital signs, ECGs, etc.
Review laboratory results, ECGs, and other test results (e.g., MRIs) for completeness and alert values, ensuring investigator review in a timely fashion.
Identify adverse events (AEs) and Serious Adverse Events (SAEs) and promptly notify Principal Investigator and Sponsor (where appropriate)

Documentation:
Record data legibly and enter in real time on paper or e-source documents
Accurately record study medication inventory, medication dispensation, and patient compliance.
Resolve data management queries and correct source data within sponsor provided timelines
Assist regulatory personnel with completion and filing of regulatory documents.
Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.
Physical and Travel Requirements
This is an on-site position with regional commute requirements. Regularly planned travel within the region will be required as part of the role.

Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive

What You Bring

Role Requirements:

Knowledge, Skills and Abilities:

Excellent working knowledge of medical and research terminology
Excellent working knowledge of federal regulations, good clinical practices (GCP)
Understanding of issues affecting clinical research in the identified therapeutic area of expertise
Ability and willingness to mentor and guide less experienced CRC as they develop and gain experience in all therapeutic areas
Ability to communicate and work effectively with a diverse team of professionals
Excellent organizational, prioritization and leadership skills and capabilities with a strong attention to detail
Excellent computer skills with demonstrated abilities using clinical trials database, IVR systems, electronic data capture, MS word and excel
Critical thinker and problem solver
Excellent interpersonal skills, detailed oriented and meticulous
Friendly, outgoing personality with the ability to maintain a positive attitude under pressure
High level of self-motivation and energy
Excellent professional writing and communication skills
Ability to work independently in a fast-paced environment with minimal supervision

Certifications/Licenses, Education, and Experience:

RN or LPN/LVN preferred
Research Professional Certification- CRCC preferred
Bachelor’s Degree preferred, or equivalent combination of education, training and experience.
A minimum of 5 years experience as a Clinical Research Coordinator requied
Prefer1 year of experience as a Care Access Research Clinical Research Coordinator
Recent phlebotomy experience required

Benefits (US Full-Time Employees Only)

PTO/vacation days, sick days, holidays.
100% paid medical, dental, and vision Insurance. 75% for dependents.
HSA plan
Short-term disability, long-term disability, and life Insurance.
Culture of growth and equality
401k retirement plan

Diversity & Inclusion

We serve patients and researchers from diverse cultures and communities around the world. We are stronger and better when we build a team representing the people we aim to support. We maintain an inclusive culture where people from a broad range of backgrounds feel valued and respected as they contribute to our mission. We value diversity and believe that unique contributions drive our success.

At Care Access, every day, we are advancing medical breakthroughs. We’re uniting standard patient care with cutting-edge treatments and research. Our work brings life-changing therapies to those in need and paves the way for newer and greater treatments to reach the world. We’re proud to advance these breakthroughs and work with the big players while engaging with the best

physicians and caring for patients. Our team of experts is paving the way to take this vision forward through innovation and a unique technology-enabled.

We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.

Care Access currently is unable to sponsor work visas.

Employment Statement

Care Access complies with all employment laws and regulations with respect to its employment practices, terms and conditions of employment, and pay equity and wages. Care Access does not engage in any unfair or forced labor practice and does not tolerate, under any circumstances, the use of any form of forced or involuntary labor, child labor, or human trafficking. This extends to suppliers, partners, or other third parties with whom Care Access does business. Care Access values and promotes the protection of human rights everywhere.

Job Type: Full-time

Quick Apply

Scientist jobs in Cambridge, MA

Site Manager-Dorchester, MA

Research Scientist, Integrated Pharmacology (Contract)

Research Coordinator-Brazelton Touchpoints

Analytical Chemist (Contract)

Customer Service Technician

Medical Technologist II, Blood Bank, 40 hrs Nights

Scientist

Quality Control Senior Associate (Contract) 22321

Scientist I

Research Assistant III - Carmargo Lab

Antibody Discovery- In Vitro, Director, Global Biologics

Cell Therapy Manufacturing Lead

Scientist, Protein/Antibody Purification & Analytics

Principal Analyst - Trade, Research & Monitoring, Fidelity Digital Assets℠

Principal Engineer, Hydrogeologist, or Geologist

Analytical Development Principal Research Scientist - Cell & Gene Therapy

Scientist

Forensic Scientist I - Toxicology

Lab Technician, Chryso, Wilmington - Construction Chemicals

Scientist, Immuno-Oncology

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