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Clinical Research Scientist I Jobs

Research Scientist I Jobs
By Seattle Childrens Hospital At , Seattle, 98105 $50,669 - $76,003 a year
Prior experience in a laboratory setting.
Research experience in biochemistry, molecular biology, and tissue culture techniques is highly preferred.
Bachelor's Degree in biology, microbiology, immunology, molecular biology or biochemistry.
Min to Max Hourly Salary$24.36 - $36.54 /hr
Min to Max Annual Salary$50,668.80 - $76,003.20 /yr
The union pay ranges can be found on the Seattle Children's website here: -
Clinical Research Coordinator I
By University of Alabama at Birmingham At , Birmingham
Be organized, show attention to detail, and have exceptional follow-through abilities.
Have clinical decision-making and assessment skills, enjoy face-to-face interactions with patients and study participants, and interfacing with investigators and clinicians.
Work Arrangement (final schedule to be determined by the department/hiring manager): Onsite
To collect and record preliminary data for clinical research programs.
To recruit and perform follow-up with research participants as protocols outline.
To schedule visits according to research protocols.
Clinical Research Coordinator I
By Velocity Clinical Research, Inc. At Covington, LA, United States
The Clinical Research Coodinator I conducts and manages clinical trials in accordance with the study protocol,GCP, and Velocity’s SOPs.
Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Velocity’s SOPs
Implement research and administrative strategies to successfully manage assigned protocols.
Create, collect, and submit regulatory documents to Sponsors and IRBs as required per protocol, GCP/ICH regulations, and IRB requirements.
Bachelor’s degree with 1 year of relevant experience in the life science industry OR
Associate’s degree with 2 years of relevant experience in the life science industry OR
Clinical Research Associate I - Smidt Heart Institute
By Cedars-Sinai At Los Angeles, CA, United States
Participates in required training and education programs.
1-year Clinical Research Related Experience
Join our team and use your skills with an organization known nationally for excellence in research!
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.
Clinical Research Coordinator I
By Seattle Childrens Hospital At , Seattle, 98105, Wa $55,765 - $83,637 a year
Bachelor's Degree in related discipline, or equivalent combination of education and experience.
Prior experience in research or a related field/setting.
Confirmed proficiency in a second language via successful completion of a language assessment may be required for certain departments.
Min to Max Hourly Salary$26. 81 - $40.21 /hr
Min to Max Annual Salary$55,764.80 - $83,636.80 /yr
The union pay ranges can be found on the Seattle Children's website here: -
Clinical Research Associate I (Part-Time)
By Binghamton University At Stony Brook, NY, United States

In accordance with the Title II Crime Awareness and Security Act

Research Scientist I Jobs
By Public Health Institute At , Sacramento, Ca $80,043 - $118,302 a year
Three years of relevant research and/or evaluation experience.
Bachelor’s degree required, or substitute with four additional years of related experience.
Intermediate to advanced skills in MS Office Word, Excel, and PowerPoint.
Research or evaluation experience with quantitative statistical software, such as SAS, SPSS, or R.
Demonstrated abilities of independent work, scientific reasoning, verbal presentation of scientific data, and production of written reports and/or scientific publications.
Substantial experience with evaluation-related technical assistance to local agencies.
Clinical Laboratory Scientist I/Ii - Generalist And Lis
By County of Riverside At , Moreno Valley, 92555, Ca
Please ensure your resume reflects your laboratory experience in specialty areas, LIS or as a Generalist.
Generalist positions - Evening shift 3pm-11:30pm; Graveyard shift 11pm-7:30am rotating holidays/weekends
Laboratory Information Systems - day shift with periodic on-call schedule required
Per diem evening shift opportunities as well
Riverside University Health System (RUHS)
Riverside University Health System-Medical Center
Clinical Research Coordinator I
By Inova Health System At , , Va
Explains and performs non-GCP related study management activities.
Competitive salary: Pay based experience
Two years patient care experience or one year clinical research experience with a bachelor's degree
Masks are provided to patients entering our buildings, and offered free to visitors
What We Have to Offer
See Full List of Benefits Here: 2022 INOVA BENEFITS GUIDE
Research Scientist I Jobs
By Public Health Institute At Greater Sacramento, United States
Three years of relevant research and/or evaluation experience.
Bachelor’s degree required, or substitute with four additional years of related experience.
Intermediate to advanced skills in MS Office Word, Excel, and PowerPoint.
Research or evaluation experience with quantitative statistical software, such as SAS, SPSS, or R.
Demonstrated abilities of independent work, scientific reasoning, verbal presentation of scientific data, and production of written reports and/or scientific publications.
Substantial experience with evaluation-related technical assistance to local agencies.
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
Clinical Research Associate I - Hybrid/Remote
By Talentify.io At United States
Knowledge of clinical research study processes, protocol management, and regulatory guidelines.
Proficiency in medical terminology and computer skills.
Strong attention to detail and excellent written and oral communication skills.
Ability to manage multiple deadlines and prioritize tasks effectively.
Minimum three years of experience in conducting clinical research studies or verifying clinical data.
Knowledge across multiple therapeutic areas, including blood and marrow transplant.
Clinical Research Scientist Jobs
By BioSpace At Arlington, VA, United States
Excellent organization, time management, ability to meet deadlines
Excellent oral, written, and interpersonal communication skills
3-5 years of clinical research experience required
Prior biomedical device development experience preferred
Work closely with the Medical Director and Clinical Research leader (as needed)
Assist to execute the clinical trial as indicated in the clinical development plan (CDP)
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.
0-2 years of 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.
Secures, delivers and ships clinical specimens as required by the protocol.
Clinical Research Associate I
By Exact Sciences At United States
Excellent organizational, time management, and problem-solving skills.
Support and comply with the company’s Quality Management System policies and procedures.
Basic proficiency of ICH GCP and monitoring practices with a track record for ensuring quality data and performing outstanding site management.
Supports the Clinical Study Manager to develop study-specific training materials.
Conducts thorough site qualifications visits. Ensures all required information concerning site/staff qualifications is clearly documented and communicated to project teams.
Works with clinical study manager to manage vendors (ie. Central Laboratory, CRF printers, CROs, etc).
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.
Clinical Research Coordinator I-Personalized Med
By Mount Sinai Health System At United States
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
Collect and record study data and input all information into a database.
Assist in IRB/GCO applications as needed.
Collect, process, deliver and ship clinical specimens as required by the protocol.

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