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Clinical Research Project Coordinator Jobs in California

Project Assistant - Clinical Research
By Registry Ally At Los Angeles, CA, United States
Must have Strong Data Entry Skills
1+ years of strong data entry skills and attention to details
Provide support to the Project Managers when it comes to transcriptions & clinical research
Experience in a Medical or Laboratory setting preferred
On-site in Van Nuys, CA office
Update spreadsheets, databases, and Case Report Forms (CRF & ECRF)
Clinical Research Project Manager
By Proper Career Solutions At Los Angeles, CA, United States
• MT Group is a CRO for biospecimen sample acquisition and management
1+ years experience in any of the following:
• 2+ years of experience in a science, research, or medical setting
• Full Benefits (Medical, Vision)
As a research coordinator or research associate
• Small, Growing Company (30 people)
Clinical Research Project Manager
By Crowdstaffing powered by Prosperix At South San Francisco, CA, United States
Bachelor's degree or equivalent practical experience. 3-5 years of experience working in project management or similar discipline.
Strong working knowledge of project management tools such as spreadsheets, Google Docs, and Project tracking software.
Knowledge and experience of clinical trials.
Excellent communication skills, with experience in communication with executives.
Proven ability to manage complex projects involving multiple stakeholders, and in a fast pace environment.
Strong problem-solving and analytical skills, and ability to handle ambiguity and create order out of it.
Clinical Project Coordinator - 122977
By UC San Diego Health At San Diego, CA, United States
Strong knowledge of investigational protocols (data management, query resolution, protocol design and protocol implementation). Working knowledge of medical and scientific terminology.
Experience performing clinical research duties in a clinical research environment such as CRO, academic research institution, and/or a research hospital.
Strong experience with research protocol in order to screen patients for eligibility, initiate treatment plan, collect specimens, and orient participating physicians.
Strong knowledge of experimental protocols, data gathering, protocol design and evaluation.
Strong experience in clinical trials research.
Experience completing clinical trials case report forms via hard copy and online.

Are you looking for an exciting opportunity to join a dynamic team of clinical research professionals? We are seeking a Clinical Research Project Coordinator to join our team and help us advance our mission of providing innovative treatments to improve patient outcomes. As a Clinical Research Project Coordinator, you will be responsible for managing the day-to-day operations of clinical research projects, including data collection, analysis, and reporting. You will also collaborate with other departments to ensure the successful completion of projects. If you are a highly organized and detail-oriented individual with a passion for clinical research, this could be the perfect job for you!

Overview A Clinical Research Project Coordinator is a professional who is responsible for coordinating and managing clinical research projects. They are responsible for ensuring that the research is conducted in accordance with the protocols and regulations set by the regulatory bodies. They are also responsible for ensuring that the research is conducted in a timely and efficient manner. Detailed Job Description A Clinical Research Project Coordinator is responsible for coordinating and managing clinical research projects. They are responsible for ensuring that the research is conducted in accordance with the protocols and regulations set by the regulatory bodies. They are also responsible for ensuring that the research is conducted in a timely and efficient manner. They are responsible for the day-to-day operations of the research project, including the recruitment of participants, the collection of data, the analysis of data, and the reporting of results. They are also responsible for ensuring that the research is conducted in a safe and ethical manner. Job Skills Required
• Excellent organizational and communication skills
• Ability to work independently and as part of a team
• Knowledge of clinical research protocols and regulations
• Knowledge of data collection and analysis techniques
• Knowledge of medical terminology
• Ability to manage multiple projects simultaneously
• Ability to work under pressure and meet deadlines
Job Qualifications
• Bachelor’s degree in a related field such as healthcare, science, or research
• Previous experience in clinical research
• Certification in clinical research
Job Knowledge
• Knowledge of clinical research protocols and regulations
• Knowledge of data collection and analysis techniques
• Knowledge of medical terminology
• Knowledge of clinical research software
Job Experience
• Previous experience in clinical research
• Experience in project management
• Experience in data collection and analysis
Job Responsibilities
• Coordinate and manage clinical research projects
• Ensure that the research is conducted in accordance with the protocols and regulations set by the regulatory bodies
• Recruit participants for the research project
• Collect and analyze data
• Report results of the research
• Ensure that the research is conducted in a safe and ethical manner
• Manage multiple projects simultaneously
• Meet deadlines and work under pressure