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Clinical Research Scientist I Jobs in Massachusetts

Scientist I/Ii - Translational Research And Operations - 2386
By Editas Medicine At Cambridge, MA, United States
Manage day to day activities of a direct report
Maintain up to date knowledge of advancements in the field including new laboratory techniques and technologies
PhD in immunology or related field with 0 to 3 years of industry experience
In depth knowledge of CRISPR based gene editing
Hands on experience with protein and cell-based assays including mammalian tissue culture, ELISA, MSD, and flow cytometry
Hands on experience with molecular biology techniques including expression systems
Senior Clinical Research Scientist
By ŌURA At Boston, MA, United States
Excellent project management skills, including the ability to prioritize tasks, manage timelines, and meet deadlines
Establish and manage research partnerships with academic organizations, healthcare institutions, commercial partners, and key opinion leaders to foster collaborative research initiatives
Ensure compliance with regulations, ethical guidelines, and data privacy requirements throughout the research process
Strong understanding of research design, methodologies, and regulatory requirements
Exceptional written and verbal communication skills, with the ability to effectively present complex scientific concepts to both technical and non-technical stakeholders
Experience in building, managing and/or mentoring a team of researchers is highly desirable
Research Scientist I, Cancer Biology
By BioSpace At Boston, MA, United States
PhD degree in a scientific discipline, or MS with 4+ years experience, or BS with 6+ years experience
Experience leveraging molecular/genetic tools for studying chromosomal/genome instability
Experience with data analysis software
What Takeda Can Offer You
and Long-Term Incentive benefits. Employees are eligible to participate in
Contribute to pre-clinical projects by developing well-defined mechanistic experiments and projects.
Senior Research Scientist I; Process Development Science
By Curia At Hopkinton, MA, United States
Provide general lab support and management.
Communicate project updates and technical reports to supervisor and senior level management.
Experience in protein purification along with the knowledge of AKTA systems is a must.
Experience with Octet, TFF systems, HPLC/UPLC is a plus.
SME for purification of biomolecules using mammalian and/or insect systems.
Lead direct reports in upstream process development.
Research Scientist I- Midas Project
By Broad Institute of MIT and Harvard At Cambridge, MA, United States
Strong interpersonal, communication, organizational and time-management skills
Strong scientific standing and background knowledge.
Strong publication record and diverse research skills is required.
Extensive experience with cell culture, molecular biology, recombinant DNA and protein biochemistry is required.
Experience and willingness to work with animals is strongly preferred, with experience generating humanized mice highly desirable.
Experience with isolation and differentiation of primary human immune progenitors is desirable.
Research Scientist I, Oncology Cell Therapy Innovation
By Takeda At Boston, MA, United States
Demonstrate broad technical program knowledge
Demonstrate effective project engagement skills
Identify, plan and execute novel scientific projects and may manage the work of others a direct or matrixed structure
Independently manage workload and expectations
Receive high level instructions on all work, determine methods on new assignments, work closely with manager, may manage junior staff
A minimum of 0- 2+ years of relevant pharmaceutical industry/academic experience is required after graduation.
Clinical Research Scientist Jobs
By SRG At Boston, MA, United States
Strong project management skills required, with demonstrable track record of success managing multiple projects simultaneously with minimal supervision.
Advanced technical writing skills is required, with demonstrated experience in writing PMCF plans / reports
Maintain strong understanding of evolving post-market evidence requirements under EU Medical Device Regulation.
Previous experience developing strategies to generate clinical evidence is strongly preferred
Develop and write high quality Post-market Clinical Follow-up PMCF plans and reports with minimal supervision.
ED&I: Impellam Group and its brands are equal opportunity employers committed to diversity and inclusion.
Research Scientist I/ Research Scientist Ii, Oncology Cell Therapy Innovation
By BioSpace At Boston, MA, United States
Demonstrate broad technical program knowledge
Demonstrate effective project engagement skills
Identify, plan and execute novel scientific projects and may manage the work of others a direct or matrixed structure
Independently manage workload and expectations
Receive high level instructions on all work, determine methods on new assignments, work closely with manager, may manage junior staff
A minimum of 0- 2+ years of relevant pharmaceutical industry/academic experience is required after graduation.
Post Market Clinical Research Specialist I
By Boston Scientific At Marlborough, MA, United States
In collaboration with PMCF management, supports the planning, execution and management of schedules for PMCF activities.
Manages internal and external project materials and timelines.
Bachelor’s degree and 1+ years of related work experience in a clinical/scientific field.
Excellent problem solving and analytical skills.
Strong verbal and written communication skills.
Collaborates to create and maintain documentation (such as plans, protocols, reports) for PMCF surveys, focus groups, and retrospective data reviews.
Clinical Research Scientist Jobs
By Abiomed At Danvers, MA, United States
1-3 years lrelevant post-graduate research experience preferred
Clinical science/research experience in cardiology/cardiovascular space or medical devices preferred
Strong work ethic, self-motivated, team player with excellent English written and oral communication skills and strong interpersonal skills
Support execution of Abiomed’s scientific objectives within Abiomed-sponsored clinical studies
Support protocol development, revisions, submission, and approval, including collaboration with study steering committee and principal investigators and communication with FDA
Support the production of trial-related interim analyses, hypothesis testing, publications, and presentations
Clinical Research Coordinator I With Transplantation
By Beth Israel Lahey Health At Burlington, MA, United States
Implements assigned research studies by reviewing study and assessing protocol and institutional requirements:
Ensures appropriate training and certification for all members of the study team involved in the research protocol.
Works collaboratively with research finance to process clinical trial agreements, study budget development and other finance issues, as applicable.
Conducts assigned research studies per protocol requirements, departmental and institutional policy:
Participates in and actively seeks continuing education opportunities.
Maintains required continuing education credits per institutional and departmental SOPs.
Research Scientist I - Sabeti Lab
By Broad Institute of MIT and Harvard At Cambridge, MA, United States
Support the development of project budgets and works with Institutional administrative staff in the close management of those budgets
Experience assessing new technologies and approaches as well as matching novel technologies with biomedical or public health applications
Experience in leading diagnostic products from early development through deployment/implementation work
Experience working in the scientific or global health field, ideally in Africa
Experience in regulatory review and approvals is a plus
Makes substantial contributions to determining goals, objectives, and research methods for new and existing projects.

Are you looking for a challenging and rewarding career in clinical research? We are looking for a Clinical Research Scientist I to join our team and help us develop innovative treatments for a variety of diseases. As a Clinical Research Scientist I, you will be responsible for designing and executing clinical trials, analyzing data, and reporting results. You will also be involved in the development of new therapeutic strategies and the evaluation of existing treatments. If you are passionate about making a difference in the lives of patients, this is the job for you!

Overview Clinical Research Scientist I is a professional who is responsible for conducting clinical research studies and trials. They are responsible for designing, planning, and executing clinical research studies and trials, as well as analyzing and interpreting the data collected. They also provide guidance and support to other clinical research professionals. Detailed Job Description Clinical Research Scientist I is responsible for designing, planning, and executing clinical research studies and trials. They are responsible for developing protocols, collecting and analyzing data, and preparing reports. They also provide guidance and support to other clinical research professionals. They are responsible for ensuring that all clinical research studies and trials are conducted in accordance with applicable regulations and guidelines. Job Skills Required
• Knowledge of clinical research principles and methods
• Knowledge of regulatory requirements and guidelines
• Excellent organizational and communication skills
• Ability to work independently and as part of a team
• Ability to analyze and interpret data
• Ability to manage multiple projects simultaneously
• Proficiency in computer applications
Job Qualifications
• Bachelor’s degree in a related field
• At least two years of experience in clinical research
• Certification in clinical research (e.g., CCRA, CCRP, etc.)
Job Knowledge
• Knowledge of clinical research principles and methods
• Knowledge of regulatory requirements and guidelines
• Knowledge of medical terminology
• Knowledge of clinical trial design and implementation
• Knowledge of data analysis and interpretation
Job Experience
• At least two years of experience in clinical research
• Experience in designing, planning, and executing clinical research studies and trials
• Experience in analyzing and interpreting data
• Experience in preparing reports
Job Responsibilities
• Design, plan, and execute clinical research studies and trials
• Develop protocols and collect data
• Analyze and interpret data
• Prepare reports
• Provide guidance and support to other clinical research professionals
• Ensure that all clinical research studies and trials are conducted in accordance with applicable regulations and guidelines