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Apex Clinical Research Associate Jobs in Santa Clara, California

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 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:
Cra (Clinical Research Associate)
By Agilent Technologies At Santa Clara, CA, United States
Assist with site audits and site quality management activities, as needed.
Please update the minimum qualifications below to reflect the requirements for your specific role.
Ensure monitoring activities (remote and on-site) are completed in accordance with Agilent procedures and study monitoring plan.
Assures adherence to GCP, study protocol, and all applicable requirements through routine monitoring visits.
3+ years direct clinical research experience at a sponsor or CRO as a CRA/study monitor, or equivalent experience.
Diagnostic/IVD experience highly preferred, oncology or other medical device experience is also accepted.
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
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).
Data Analyst (Apex Legends)
By Respawn Entertainment At Los Angeles, CA, United States
You will communicate results to designers, product managers, analysts, and others throughout the organization.
At least 3 years of relevant experience
Experience with applied statistics and advanced analytics.
Strong knowledge of Power BI
Experience creating compelling data stories for partners.
Experience managing a small team
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 ...

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).
Clinical Research Associate I
By Nevro Corp. At , Redwood City, 94065, Ca $67 an hour
2 years of related experience in supporting medical device clinical trials
Strong interpersonal and communication skills
Able to manage multiple tasks
Experience working directly with US and EU sites strongly desired
Experience working with clinical data and databases (desirable)
Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation

Are you looking for an exciting opportunity to join a dynamic team of clinical research professionals? Apex Clinical Research is looking for a Clinical Research Associate to join our team and help us make a difference in the lives of patients. As a Clinical Research Associate, you will be responsible for managing clinical trials, ensuring compliance with regulatory requirements, and providing support to clinical teams. If you have a passion for clinical research and want to make a difference, this is the job for you!

Overview Apex Clinical Research Associates are responsible for conducting clinical research studies in a variety of settings. They are responsible for collecting and analyzing data, preparing reports, and presenting findings to stakeholders. They must be knowledgeable in clinical research protocols and regulations, and must be able to work independently and collaboratively with other members of the research team. Detailed Job Description Apex Clinical Research Associates are responsible for conducting clinical research studies in a variety of settings. They are responsible for designing and implementing research protocols, collecting and analyzing data, preparing reports, and presenting findings to stakeholders. They must be knowledgeable in clinical research protocols and regulations, and must be able to work independently and collaboratively with other members of the research team. They must also be able to communicate effectively with research participants and other stakeholders. Job Skills Required
• Knowledge of clinical research protocols and regulations
• Ability to design and implement research protocols
• Ability to collect and analyze data
• Ability to prepare reports and present findings
• Ability to work independently and collaboratively
• Excellent communication and interpersonal skills
Job Qualifications
• Bachelor’s degree in a related field
• Previous experience in clinical research
• Knowledge of clinical research protocols and regulations
• Ability to design and implement research protocols
• Ability to collect and analyze data
• Ability to prepare reports and present findings
• Ability to work independently and collaboratively
• Excellent communication and interpersonal skills
Job Knowledge Apex Clinical Research Associates must have a comprehensive understanding of clinical research protocols and regulations. They must be knowledgeable in the design and implementation of research protocols, data collection and analysis, and report preparation and presentation. Job Experience Apex Clinical Research Associates must have previous experience in clinical research. They must be able to work independently and collaboratively with other members of the research team. Job Responsibilities
• Design and implement research protocols
• Collect and analyze data
• Prepare reports and present findings
• Communicate effectively with research participants and other stakeholders
• Ensure compliance with clinical research protocols and regulations
• Work independently and collaboratively with other members of the research team