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Field 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
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 (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.
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 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 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 Jobs
By USC At , San Diego, Ca $42.26 - $52.60 an hour
Confirm sites are following GCP, regulatory requirements, study protocol, and ATRI policies. Work with sites to document deviations from standard procedures.
Experience in AD research is preferred.
Act as main point of contact for assigned clinical sites.
Thorough understanding of study protocol and manuals.
Work closely with Lead Clinical Monitor/Lead CRA to escalate site compliance issues.
Participate in monitoring activities to achieve study milestones.
Clinical Research Associate Jobs
By Infosoft, Inc. At Irvine, CA, United States
Solid understanding and knowledge of principles, theories, and concepts relevant to clinical trial management
3 years of previous hands-onclinical researchexperience
Good computer skills in usage of MS Office Suite including MS Project and excellent Excel skills required
Excellent written and verbal communication skills and interpersonal relationship skills
Solid knowledge of human anatomy and physiology
Good problem-solving, organizational, analytical, and critical thinking skills
Clinical Research Associate Jobs
By BioPhase At San Diego Metropolitan Area, United States
Conduct study site selection, qualification, training, start up, and close out .
Assist with data entry as necessary.
-A minimum of 2 years' direct experience in clinical study monitoring is required.
-Experience in IVD studies is preferred, with a proven track record of progressive clinical study responsibility.
-Knowledge of medical terminology and good clinical practice required.
Detail-oriented with a high level of organizational skills.
Clinical Research Associate Jobs
By Ansun BioPharma Inc At , San Diego, 92121, Ca $75,000 - $95,000 a year
Qualification / Education/ Experiences/ Skills
Late-stage clinical trial experience and working knowledge of US regulatory agency requirements, preferred
Conduct medical monitoring, pharmacovigilance, regulatory, data management related to delegated clinical study.
Manage investigational product (IP) accountability and reconciliation process
Minimum BA/BS in scientific, life science, or related field with 2+ years CRA related experiences
Sponsor-side clinical trial experience in the pharmaceutical industry is preferred
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 Rangam At Alameda County, CA, United States
Bachelor’s degree REUIRED WITH A PREFERANCE IN Biological Sciences which fit best BUT “Life Sciences” degrees will also be considered
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
Will be doing monitoring visits
Medical device exp. of at least 1 year
Clinical Research Associate Jobs
By Intellectt Inc At Alameda, CA, United States
• 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
• Medical device exp. of at least 1 year
Clinical Research Associate Ii
By Labcorp At , San Diego, 92128, Ca $90,000 - $125,000 a year
Thorough knowledge of ICH Guidelines and understanding of local regulatory requirements
Thorough knowledge of monitoring procedures; Basic understanding of the drug accountability process
Good planning, organization and problem-solving abilities; Ability to work with minimal supervision
Organize and make presentations at Investigator Meetings
Participate in the development of protocols and Case Report Forms as assigned
Negotiate study budgets with potential investigators and assist the Covance legal department with statements of agreements as assigned
Clinical Research Associate Jobs
By iCell Gene Therapeutics At Stony Brook, NY, United States
At least two years of experience as a clinical research associate
Excellent writing, editing, and communication skills
Strong Administrative and Organizational skills to support several team members
A bachelors degree in Health Sciences, Nursing or Medical Biotechnology, or Biological Sciences
Familiarity with various computer document formats, styles, and standards
· Collecting, analyzing, and recording data
Clinical Research Associate Jobs
By Juno Search Partners At Greater Philadelphia, United States
Able to manage multiple and competing priorities through effective organizational management skills.
Effective interpersonal skills; able to build effective relationships with study management team colleagues and business partners.
Excellent time management skills; able to accomplish established goals efficiently.
Supply chain management support may include:
Support Trial Management team member with assigned study specific projects and tasks.
Two years Clinical Research work experience, or relevant experience
Clinical Research Associate Jobs
By Talencio At Greater Minneapolis-St. Paul Area, United States
Clinical Trial Collaboration: Work alongside our clinical team, focusing on site qualification, initiation, management, and data integrity.
Data Management: Oversee data activities, generate, and resolve queries, and report on study metrics including enrollment and adverse events documentation.
Regulatory Oversight: Manage investigational product accountability, monitor IRB requirements, and ensure prompt processing of regulatory documents.
Bachelor’s degree in a medical/scientific field, with 4+ years of clinical research experience (Master’s degree can substitute for 1 year).
Strong organizational, multitasking, and relationship-building abilities.
Effective communication skills and keen attention to detail.
Clinical Research Associate Jobs
By Lumicity At Austin, TX, United States
5+ years of CRA experience.
3+ years of experience working on oncology studies.
BS in a relevant scientific discipline.
Ability to travel and be on-site. (Austin, TX or Portland, OR).
6-month contract. - 40 hours per week. - Monday to Friday.
Austin, TX or Portland, OR
Clinical Field Specialist Jobs
By Natera At Montana, United States
Effective time management skills required with a demonstrated ability to assess and prioritize opportunity required.
Market knowledge and experience selling to OB/GYN or MFM strongly preferred.
Minimum three years’ physician sales experience in diagnostic laboratory business (preferably in a genetics laboratory).
Excellent organizational and communication skills (written and verbal) with demonstrated ability to effectively present to both internal and external customers.
Increasing revenue and driving market development through direct sales to individual MFMs, Ob/Gyns and Genetic Counselors.
Sales efforts include effective prospecting, cultivating and maintaining key relationships.
Ophthalmology Clinical Research Associate
By SRG At United States
Minimum of four (4) years of experience in clinical research specifically in Ophthalmology surgical medical devices.
Experience in glaucoma devices is strongly preferred.
Knowledge of medical and ophthalmology terminology
Remotely monitor data and support clinical sites for protocol compliance and recruitment activities
Manage clinical trial close-out activities, including return of investigational product, final reconciliation of all required documentation, and EDC close-out
** Candidates must have experience in Ophthalmology Clinical Research trials to be considered!
Clinical Research Associate Jobs
By Brain Tumor Network At Ponte Vedra Beach, FL, United States
• Maintains on-going professional education on clinical trials and research
• Minimum requirement: master’s degree in nursing/Healthcare related field
• Clinical work experience in oncology
• Excellent organizational and communications skills, with team-player proven ability to meet project deadlines
• Knowledge of data analytics
• Serves as a liaison to industry sponsored, consortium and Investigator initiated Brain Tumor Trials
Clinical Research Associate Jobs
By AstraZeneca At , Wilmington, 19803
Good understanding of Clinical Study Management including monitoring, study drug handling and data management
1.5+ years of CRA experience in Cardiovascular/Metabolic, Respiratory and/or Immunology therapeutic experience
Fluent knowledge of spoken and written English
Excellent knowledge of international guidelines ICH/GCP, basic knowledge of GMP/GDP
Good knowledge of relevant local regulations
Good medical knowledge in relevant AZ Therapeutic Areas
Clinical Research Associate/Site Manager
By Relmada Therapeutics, Inc At United States
·3+ years of clinical monitoring or site management experience.
Delivers high quality and timely reports following each site management or site monitoring visit.
May include managing query resolution process with clinical sites and data management groups.
·Thorough knowledge and understanding of ICH/GCPs and applicable regulatory requirements.
·Solid computer skills, including working knowledge of Microsoft Office applications (Word, Excel Outlook, etc.).
Prepares for and conducts site qualification and site initiation, visits. May also include interim and closeout monitoring visits.
Clinical Research Associate Jobs
By Candel Therapeutics At , Needham, 02494
Knowledge of project management tools and practices, and proficiency in using normal office software; Microsoft Word, Excel and PowerPoint.
Participate in maintaining accuracy within clinical management systems and internal reports and trackers.
Able to manage multiple projects independently and use varying databases and management systems.
Minimum 1-3 years relevant clinical research experience.
Excellent verbal and written communication skills, good organizational and interpersonal skills, and a team drive.
Knowledge of GCP and FDA regulations related to clinical trial conduct and familiarity with industry best practices.
Clinical Research Associate Jobs
By Balt USA At , Irvine
Experience in clinical study management required.
Manages Trial Management Filing (TMF) system, including document inspection, filing, and auditing.
Serves as key facilitator and liaison for shipping, receiving, and management of study devices.
Ability to constructively interact directly with senior management teams.
Recognition of work, respect, and our multicultural community are key aspects of the employee experience and contribute to our continued success.
Manages study and site materials, including, but not limited to study binders, study trackers, training documentation.
Clinical Research Associate Ii
By BeiGene At , Remote $90,500 - $120,500 a year
Familiar with industry CTMS and data management systems
Provides site level management for established protocols and portfolio under general supervision
Project Management - Communicates changes and progress; Completes projects on time and budget.
Serve as mentor/trainer for less experienced CRAs to assist with general and study-specific monitoring issues
Understands clinical trial processes with a thorough knowledge of ICH and associated regulatory guidelines
Excellent communication and interpersonal skills
Clinical Research Associate Jobs
By Philips At , Cambridge
Shipping/ labeling/Site Management and Team meeting facilitator
Database Lock (listing review as needed/ Data query & resolution/Source data verification – onsite or remotely)
Read more about our employee benefits.
Generation of Study Documents (Clinical Monitoring Plans/ Informed Consents/ data source work sheets/Device accountability/training slides and work instructions)
Site start up to Site Activation (SA) to include Investigator Site File/Inventory and Device
Study Duration (Enrollment tracking/Key Performance Indicators/Adverse Events/ Serious Adverse Events)
Clinical Research Associate (Fsp) - Poland
By Parexel At United States
Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology.
Excellent time management and social skills
Minimum of 2 years of active independent field monitoring experience - all types of visits.
Strong interpersonal, written, and verbal communication skills within a matrixed team.
Experience working in a self-driven capacity, with a sense of urgency and limited oversight.
Benefits Of Working With Parexel FSP
Clinical Research Associate (Cra)
By Merck Sharp & Dohme At , Guaynabo
Proven Skills in Site Management, including management of site performance and patient recruitment.
Effective time management, organizational and interactive skills, conflict management, problem solving skills.
Performs clinical study site management/monitoring activities;
Performs remote and on-site monitoring & oversight activities.
Works in partnership with GCTO country operations, finance, regulatory affairs, pharmacovigilance, legal and regional operations;
Mininum 2 years of direct site monitoring experience in a bio/pharma/medical industry.
Clinical Research Associate Jobs
By HemoSonics, LLC At , Durham, 27703
Experience in clinical research protocols, reporting, regulatory submissions, development of monitoring/analysis/data management plans with technical support
Strong written, oral, and interpersonal communication skills including proficient knowledge of medical terminology
Ability to identify customer requirements and manage expectations for clinical studies
ESSENTIAL JOB DUTIES AND RESPONSIBILITIES
Strong knowledge of World Health Organization (WHO) Good Clinical Practice (GCP) and International Conference on Harmonization (ICH)
Working knowledge of clinical research methods and practices for medical devices, including IDE and CE Mark studies.
Clinical Research Associate Jobs
By ImmunityBio, Inc. At Home Creek, VA, United States
Detail oriented, with solid organization and time management skills
Serve as Subject Matter Expert for clinical sites including providing guidance on protocol interpretation and eligibility requirements
Provide guidance to sites including protocol interpretation and eligibility requirements
Conduct site visits including (but not limited to) site qualification visit, site initiation visits, interim montoring visits, study close-out visits.
Train vendors, investigators, and study coordinators on study requirements and provide guidance on site issues as needed
Train sites on specimen and shipment requirements for central laboratory and serve as liaison with contracted vendors
Clinical Research Associate - Sponsor Dedicated
By IQVIA At , Remote
Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.
Effective time and financial management skills.
Alternatively, you should have an equivalent combination of education, training and experience
A Bachelor's degree in a health care or other scientific discipline or educational equivalent
Good therapeutic and protocol knowledge as provided in company training.
Written and verbal communication skills including good command of English language.