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: $84.2K - $107K a year
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Clinical Data Manager
Osprey Life Sciences —Cambridge, MA
Engage with both clinical and technical teams. Proven track record of driving successful SDLC projects. Author, develop, and maintain key project documents.
$135,000 - $155,000 a year
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5h
Senior Environmental Engineer or Scientist
Integral Consulting Inc. —Boston, MA
Candidates should hold a B.S. or M.S. degree in hydrogeology, geology, environmental science, environmental or civil engineering, or related technical field;…
$105,000 - $165,000 a year
R&D Manager
Kayem Foods, Inc. —Chelsea, MA
One thing will never change, it’s our “Old World” food philosophy: to only make food we would share with our own friends and family.
Estimated: $90.7K - $115K a year
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6h
PLM Analyst/Scientist
Pace® Analytical Services —Woburn, MA
Bachelor's degree in Geology, or a closely related field. Visual acuity to read, to determine color, depth perception and field of vision.
Estimated: $45.9K - $58.1K a year
Associate Scientist
Validation Associates —Cambridge, MA
Monitors or follows established experimental design and protocols and performs routine tasks and studies to obtain reproducible and reliable results with…
$30 - $35 an hour
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12h
Director, Sensor Design & Development
Medica Corporation —Bedford, MA
The Director, Sensor Design and Development leads a team of scientists to conduct analytical research and development for state of the art potentiometric,…
From $160,000 a year
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11d
Antibody Licensing Scientist
Biocytogen Boston —Waltham, MA
Communication Skills: Excellent verbal and written communication skills, with the ability to convey complex technical information to a non-technical audience.
$85,000 - $110,000 a year
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8d
Lab Technician I (MA) - Science background and degree required.
Green Analytics LLC —Framingham, MA
Bachelor’s degree in Chemistry or a related field from an accredited college. POSITION SUMMARY:* This is an entry level position responsible for the collection…
$20 an hour
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12d
Senior Manager, GCP Operational Quality Assurance R&D (Remote)
Vertex Pharmaceuticals —Boston, MA
For assigned programs/ studies, leads quality issue investigations, root cause analysis and CAPA development and assist study teams in implementing corrective…
$132,880 - $199,320 a year
20h
Staff Scientist- Early Childhood Development
Boston Children's Hospital —Boston, MA
Daily project management & implementation of evaluation design, data collection & management, data analysis, and reporting; resource delegation, team management…
Interim Skilled Nursing Facility Clinical Manager/Documentation Regulatory Specialist
Kirby Bates Associates —Massachusetts
Massachusetts RN license required (Massachusetts is not a compact state). The complex provides amenities including a library, dry cleaning, barber shops, an…
$195,000 - $208,000 a year
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Laboratory Assistant
INTEGRA TESTING SERVICES —Needham Heights, MA
High school diploma or equivalent; additional education or certification in medical laboratory technology is preferred. Skill in written and oral communication.
$20.44 - $25.00 an hour
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Sr Research Associate
Cabot Corporation —Billerica, MA
Knowledge of basic principles in one of the specified fields: materials science, electrochemistry, electrocatalysis, interface & colloid science, polymer…
Payment Policy Analyst
Point32Health —Canton, MA
Experience in coding is required; certified coder (CPC, COC, RHIT, CCS, or CCS-P) is a plus, certification is required within 1 year of hire.
Estimated: $71.4K - $90.5K a year
Quick Apply
Analytical Development Scientist - Cell & Gene Therapy
Vertex Pharmaceuticals —Boston, MA
Provide expertise in experimental design, data analysis, assay trouble shooting, technical report writing, and presentations.
Estimated: $115K - $145K a year
Process Development Engineering Scientist - Cell Therapy
Vertex Pharmaceuticals —Boston, MA
Experience in design of experiments (DOE) and statistical analysis. Direct industry experience developing cell therapies for early and/or late phase clinical…
Estimated: $115K - $146K a year
Process Dev Engineering Research Associate (Contract)
Vertex Pharmaceuticals —Boston, MA
Hands-on experience with typical cell processing equipment used in cell therapy manufacturing. Bachelor's degree in a relevant field is required.
$30 - $32 an hour
Lab Technician
Actalent —Waltham, MA
Cell therapy, t cell, GMP, batch record, batch record review, biologics, tcr, validation, manufacturing technician, Lab Technician, Laboratory Technician, cell…
$33 - $44 an hour
Quick Apply
5d
Scientist - Discovery Neuroinflammation Group
Pfizer —Cambridge, MA
Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process…
$74,900 - $124,800 a year
7d

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Site Manager-Dorchester, MA

Care Access - Dorchester, MA

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Job Details

Full-time Estimated: $84.2K - $107K 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.

Job Type: Full-time

Quick Apply

Scientist jobs in Cambridge, MA

Site Manager-Dorchester, MA

Clinical Data Manager

Senior Environmental Engineer or Scientist

R&D Manager

PLM Analyst/Scientist

Associate Scientist

Director, Sensor Design & Development

Antibody Licensing Scientist

Lab Technician I (MA) - Science background and degree required.

Senior Manager, GCP Operational Quality Assurance R&D (Remote)

Staff Scientist- Early Childhood Development

Interim Skilled Nursing Facility Clinical Manager/Documentation Regulatory Specialist

Laboratory Assistant

Sr Research Associate

Payment Policy Analyst

Analytical Development Scientist - Cell & Gene Therapy

Process Development Engineering Scientist - Cell Therapy

Process Dev Engineering Research Associate (Contract)

Lab Technician

Scientist - Discovery Neuroinflammation Group

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