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Clinical Research Associate Jobs in San Francisco, California

Clinical Research Associate Jobs
By Vial At San Francisco, CA, United States
Site management and monitoring activities across all US clinics
Minimum of 2 years work experience as a Clinical Research Associate
You should be life science degree educated with independent on-site monitoring experience.
Flexibility and ability to travel are paramount with strong communication, written and presentation skills.
Must have experience in Dermatology and Ophthalmology studies.
Work with sites to adapt, drive and track subject recruitment plan
Senior Clinical Research Associate
By Olema Oncology At , San Francisco, Ca $143,170 - $158,104 a year
Advanced site monitoring; study site management; and registry administration skills.
Substantial site management experience or equivalent experience in clinical research, with an understanding of clinical trials methodology and terminology.
Manage vendors to ensure timely and quality deliverables. Develop trackers for sample management.
Comfortable working with different levels of the company including senior level management.
Participate in preparation of vendor requirements and project scope and selection of study vendors.
Manage recruitment and enrollment metrics, provide weekly study updates and slides for Clinical Development.
Clinical Research Associate Jobs
By FibroGen, Inc. At , San Francisco, 94158, Ca $98,000 - $113,100 a year
Manages submission of documents and maintenance of the Trial Master File (TMF); reviews TMF to ensure inspection-readiness
At least 2 years of relevant experience in the pharmaceutical industry, Biotech or equivalent
Knowledge of GCP and ICH guidelines required
Excellent communication and interpersonal skills
Strong computer skills in MS Word, Excel, Outlook, and PowerPoint
Responsible for ensuring external service providers execute activities in a quality manner and per the established contract
Clinical Research Associate Jobs
By Integrated Resources, Inc ( IRI ) At Mountain View, CA, United States
The Clinical Research Intern will apply analytical, project management skills and enthusiasm for healthcare and commitment to improving healthcare through research.
The candidate will Product practical experience within the Clinical Research operations at ***.
Complies with established policies, health and safety regulations and requirements, procedures, and department objectives.
Bachelor's Degree in biological or life sciences or health related field OR attending/completed a clinical research certification program.
Proficient computer skills using Microsoft Office products.
May assist with follow up and closing of clinical studies.
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.
Excellent Job Opportunity For Role: Clinical Research Associate At Alameda, Ca
By Intellectt Inc At Alameda, CA, United States
Must have 5+ years of relevant experience in site monitoring, clinical project management, clinical trial practices and regulations.
Proactively and effectively communicate the status of clinical studies to management.
Clinical Operations Manager as needed
TMF upload experience is preferred.
Experience coordinating site initialization and site close
Experience editing/revising CRF "case report forms"
Clinical Research Associate (Cra) - B
By Intellectt Inc At Alameda, CA, United States
5+ years of relevant experience in site monitoring and clinical project management.
Project management and organizational skills.
Communicate study progress to management.
Understanding of clinical trial process, data management, and analysis.
Manage clinical monitoring, site compliance, and adherence to protocols.
Experience in medical device, in-vitro diagnostics, or pharmaceutical studies.
Senior Clinical Research Associate
By Collabera At Alameda, CA, United States
Experience working on Clinical Trial Research and Clinical Research Trial Documentation
Previous experience within the Medical Device or Pharma industry
5+ years’ experience in Clinical Research
Comfortable working with a lot of documentation
Bachelor’s Degree – Any life sciences related degree
Clinical Research Associate Jobs
By ProKatchers LLC At West Sacramento, CA, United States
Position Requirements: Bachelor's degree in a Life Science or related field with 2+ years’ experience in laboratory experience.
Location:West Sacramento CA 95691 United States
Pay Rate:$45/ HR to $50/ HR
Clinical Research Associate Jobs
By KlinEra Global Services At San Francisco Bay Area, United States
Excellent interpersonal, judgment, and time management
You will also manage regular site liaison, tracking, query resolution, and maintaining investigator site file and TMF.
Approximately 3-5yr Experience as Clinical Research Associate
Fundamental knowledge and good understanding of GCP’s, clinical study development process, and logistics.
Proficient knowledge of MS Office Applications (Word, Excel, PowerPoint, Etc.
Support study start-up activities including site selection, collecting essential documents and CTRA, register study on ANZCTR.
Clinical Research Associate Jobs
By Jobot At Los Angeles, CA, United States
Strong Benefits And Compensation Package
Clinical Research Associate opportunity in the oncology space!
Want to learn more about this role and Jobot?
Clinical Research Associate Ii
By DermTech At San Diego Metropolitan Area, United States
Effective time and financial management skills.
Or equivalent combination of education and experience
or equivalent combination of education and experience
Years of independent monitoring experience within a Contract Research Organization/Pharmaceutical company
Good therapeutic and protocol knowledge as provided in-company training.
Strong written and verbal communication skills including good command of the English language.
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 Jobs
By Intuitive At Sunnyvale, CA, United States
Clinical research/clinical trial management certification/education preferred
Must be clinically savvy and possess time management, organizational skills and problem-solving skills
Skills, Experience, Education, & Training:
Perform on-site (preferred) and remote (as needed) site qualification visits, site initiation visits, interim monitoring visits and close out visits.
Collaborate with data management to support CRF build, amendment, and data cleaning process.
Manage site start-up and activation process, including:
Clinical Research Associate (Cra)
By Select Source International At Alameda, CA, United States
Job Title: Clinical Research Associate (CRA) - B
• Minimum of 3 to 5 years of clinical exp. within industry
• Specifically looking for monitoring exp. on the sponsor side
• Will be supporting a multi-site study
• Exp. with site selection
• Will be doing monitoring visits
Clinical Research Associate Jobs
By Compliance Group Inc At Alameda, CA, United States

Description: Member of the clinical team responsible for conducting Phase I-IV single or multi center studies according to Federal Regulations and ICH guidelines. Responsible for assisting senior ...

Cancer Clinical Research Coordinator Associate - Hematology
By Stanford University School of Medicine At Stanford, CA, United States
Monitor expenditures and adherence to study budgets and resolve billing issues in collaboration with finance and/or management staff.
Knowledge, Skills And Abilities (required)
Ensure essential documentation and recording of patient and research data in appropriate files per institutional and regulatory requirements.
Knowledge of the principles of clinical research and federal regulations.
Previous experience with clinical research.
Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred.
Clinical Research Associate Jobs
By Aven Talent Resources At Solana Beach, CA, United States
 Manage sample inventory with superior organizational skills
 Superior molecular biology bench skills with great attention to details
 Experience with nucleic acid technologies relating to PCR and qPCR required
 Prior experience in oncology and NGS prefered
 Experience in liquid biopsy is a plus
 Experience working under design control highly desired
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).

Are you looking for a challenging and rewarding career in clinical research? We are looking for a Clinical Research Associate to join our team and help us develop and execute clinical studies. You will be responsible for managing clinical trials, ensuring compliance with applicable regulations, and providing support to investigators and sponsors. If you have a passion for clinical research and want to make a difference, this is the job for you!

Overview:

A Clinical Research Associate (CRA) is a healthcare professional who works in clinical research and is responsible for monitoring the progress of clinical trials. The CRA is responsible for ensuring that clinical trials are conducted in accordance with the protocol, applicable regulations, and ethical standards.

Detailed Job Description:

A Clinical Research Associate is responsible for the planning, coordination, and execution of clinical trials. This includes the development of study protocols, the selection of clinical sites, the recruitment of study participants, the collection and analysis of data, and the reporting of results. The CRA is also responsible for ensuring that the clinical trial is conducted in accordance with the protocol, applicable regulations, and ethical standards.

What is Clinical Research Associate Job Skills Required?

• Knowledge of clinical research principles, regulations, and guidelines
• Excellent organizational and communication skills
• Ability to work independently and as part of a team
• Ability to manage multiple tasks and prioritize work
• Attention to detail and accuracy
• Proficiency in Microsoft Office applications

What is Clinical Research Associate Job Qualifications?

• Bachelor’s degree in a related field
• Previous experience in clinical research or related field
• Certification as a Clinical Research Associate (CCRA) or Clinical Research Professional (CRCP)

What is Clinical Research Associate Job Knowledge?

• Knowledge of clinical research principles, regulations, and guidelines
• Knowledge of Good Clinical Practice (GCP)
• Knowledge of medical terminology
• Knowledge of clinical trial design and data analysis

What is Clinical Research Associate Job Experience?

• Previous experience in clinical research or related field
• Experience in monitoring clinical trials
• Experience in data collection and analysis

What is Clinical Research Associate Job Responsibilities?

• Develop and implement clinical trial protocols
• Monitor clinical trial sites to ensure compliance with protocol and applicable regulations
• Recruit and screen study participants
• Collect and analyze data
• Prepare and submit reports to regulatory agencies
• Maintain accurate and up-to-date records
• Ensure the safety of study participants