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Clinical Research Scientist I Jobs in California

Clinical Lab Scientist I, Er/Ac Laboratory - Pd
By CEDARS-SINAI At , Los Angeles, Ca
One-year experience in relevant field preferred.
Baccalaureate degree in a Clinical Laboratory Science, Medical Technology, or related science.
Clinical Laboratory Scientist license issued by the State of California.
Make a difference every single day!
What will you be doing in this role?
Senior Scientist Clinical Research
By Abbott Laboratories At , Alameda, Ca $104,300 - $208,500 a year
Knowledge of laboratory techniques consistent with a skilled, experienced professional.
The salary range for this position is 104,300 - 208,500K based on experience.
Able to perform proficiently under up to date regulatory requirements.
Experience conducting electrochemical analytical techniques.
Career development with an international company where you can grow the career you dream of.
Free medical coverage for employees* via the Health Investment Plan (HIP) PPO
Clinical Research Coordinator I
By CEDARS-SINAI At , Los Angeles, Ca $23.39 - $39.76 an hour
1 year of Clinical research related experience
Schedules patients for research visits and procedures.
Maintains accurate source documents related to all research procedures.
Responsible for accurate and timely data collection, documentation, entry, and reporting including timely response to sponsor queries.
Schedules and participates in monitoring and auditing activities.

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