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Clinical Research Scientist I Jobs

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 Coordinator I-Emergency Med
By Mount Sinai Health System At United States
Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.
1-2 years of research experience
Collects and records study data. Inputs all information into database.
Assists in preparing grant applications, IRB/GCO for submission and filings.
Secures, delivers and ships clinical specimens as required by the protocol.
Bachelors or Masters degree in Science or closely related field.
Clinical Laboratory Scientist I/Ii/Iii- Pm Shift #2969
By BioSpace At Raleigh, NC, United States
Identify process improvement opportunities and report to laboratory management.
Perform and document reagent qualifications per the approved protocols.
Participate and comply with Quality and applicable regulatory requirements.
Experience in molecular biology techniques preferred
Working knowledge of local, state and federal laboratory regulations preferred
Your Qualifications And Background Will Include
Clinical Research Coordinator I-12910-049
By Mount Sinai Health System At United States
Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.
1-2 years of research experience
Collects and records study data. Inputs all information into database.
Assists in preparing grant applications, IRB/GCO for submission and filings.
Secures, delivers and ships clinical specimens as required by the protocol.
Bachelors or Masters degree in Science or closely related field.
Clinical Research Associate I - Regenerative Medicine Institute
By Cedars-Sinai At Los Angeles, CA, United States
Participates in required training and education programs.
Understanding of general clinical research objectives. One (1) year of clinical research experience is preferred.
Ability to interpret and apply knowledge of State, Federal and Agency standards to comply with regulations.
Must possess computer skills, including Word and Excel, and the ability to use standard office equipment is required.
Assists with clinical trial budgets and patient research billing.
Completes Case Report Forms (CRFs).
Clinical Research Associate I - Remote (Usa Only)
By Abbott At Illinois, United States
Must be detail-oriented and efficient in time management.
Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol.
Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff.
Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and
Basic knowledge in regulations for applicable geographies and types of studies (IDE, non-significant risk, feasibility, exempt, etc.).
Minimum 1-year clinical research experience required.
Clinical Research Scientist Jobs
By Target ALS At United States
Manage creation of complex sample management plans to ensure proper collection and storage of samples for analysis.
Oversee LIMS system in coordination with core programmanager. Collaborate with sites to streamline and codify data entry for LIMS system.
Ensure utilization of NIH Common Data Elements into the data management scheme
Collaborate with the Grant funded Biofluid and Post-mortem core facility investigators to manage and drive growth of these core resources.
Manage Target ALS diversity initiative aimed at increasing participation of rural, under-represented and minority communities in ALS research.
Manage the biosample and dataset request approval system for Target ALS Cores.
Clinical Research Coordinator I (All Of Us)
By Mount Sinai Health System At United States
Strong communication and organization skills
Obtain informed consent and educate participants regarding study requirements.
1-2 years clinical research experience
Pristine attention to detail and ability to manage time appropriately, able to multitask in a fast-paced environment
Background in clinical research or closely related field
Passion for patient care and clinical research
Research Scientist, Clinical & Translational Research
By Caris Life Sciences At Irving, TX, United States
Previous research experience in the molecular diagnostic field of oncology is preferred.
Draft to manuscripts, conference abstracts, posters, and/or presentation slides for various audiences
Work collaboratively with internal/external researchers on editing drafts until finalization and publication.
Ph.D. in a biological science related to cancer biology, biochemistry, molecular and cellular biology or biostatistics.
Conditions of Employment: Individuals must successfully complete pre-employment process, which includes criminal background check, drug screening, and reference verification.
Strong background in biostatistics or data science is preferred.
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.
Clinical Research Coordinator I - Light & Health Research Center
By Mount Sinai Health System At United States
Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.
1-2 years of research experience
Collects and records study data. Inputs all information into database.
Assists in preparing grant applications, IRB/GCO for submission and filings.
Secures, delivers and ships clinical specimens as required by the protocol.
Bachelors or Masters degree in Science or closely related field.
Clinical Research Coordinator I - Personalized Med
By Mount Sinai Health System At United States
Obtain informed consent and educate participants regarding study requirements.
Strong communication and organization skills
1-2 years clinical research experience
Pristine attention to detail and ability to manage time appropriately, able to multitask in a fast-paced environment
Collect and record study data and input all information into a database.
Assist in IRB/GCO applications as needed.
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.
Clinical Research Associate I Prdm
By Cedars-Sinai At Los Angeles, CA, United States
Participates in required training and education programs.
Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement study.
Evaluates and abstracts clinical research data from source documents.
Ensures compliance with protocol and overall clinical research objectives.
Completes Case Report Forms (CRFs).
Enters clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors.
Clinical Research Associate I, Rosser
By Cedars-Sinai At Los Angeles, CA, United States
Participates in required training and education programs.
1 year of Clinical Research Related Experience preferred
Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement study.
Evaluates and abstracts clinical research data from source documents.
Ensures compliance with protocol and overall clinical research objectives.
Completes Case Report Forms (CRFs).
Clinical Research Coordinator I - Neurology
By Mount Sinai Health System At United States
Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.
1-2 years of research experience
Collects and records study data. Inputs all information into database.
Assists in preparing grant applications, IRB/GCO for submission and filings.
Secures, delivers and ships clinical specimens as required by the protocol.
Bachelors or Masters degree in Science or closely related field.
Clinical Research Coordinator I - Tisch Cancer Institute
By Mount Sinai Health System At United States
Assists with coordination and management of clinical trials including communication with Sponsors.
Under direct supervision of the Principle Investigator(s), obtains informed consent and educates participants regarding study requirements.
1-2 years of research experience
Experience in a hospital or academic (research) environment preferred
Excellent written and oral communication skills
Collects and records study data; inputs all information into database.
Clinical Research Coordinator I
By Mount Sinai Health System At United States
Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.
1-2 years of research experience
Collects and records study data. Inputs all information into database.
Assists in preparing grant applications, IRB/GCO for submission and filings.
Secures, delivers and ships clinical specimens as required by the protocol.
Bachelors or Masters degree in Science or closely related field.
Clinical Research Data Specialist I - Cedars-Sinai Center For Outcomes Research And Education (Cs-Core) - Part-Time
By CEDARS-SINAI At , Los Angeles, Ca $23.39 - $39.76 an hour
Participates in required training and education programs.
Experience in a similar position is highly preferred.
Maintains the accuracy, integrity and security of complex, large computerized records systems.
Understands regulations, policies, protocols, and procedures to control and maintain accurate records.
Performs data searches and other related administrative tasks.
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.
Clinical Research Coordinator I - Rehabilitation And Human Performance
By Mount Sinai At , New York, 10029, Ny $58,661 - $80,000 a year
Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.
1-2 years prior research experience
Excellent written and oral communication skills
Collects and records study data. Inputs all information into database
Assists in preparing grant applications, IRB/GCO for submission and filings.
Bachelor's or Master's degree in Science or closely related field.

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