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Associate Director Clinical Research Jobs in Mountain View, 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:
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 (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 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
Associate Director, Clinical Transplant
By CEDARS-SINAI At , Los Angeles, Ca $143,000 - $257,200 a year

Job Summary: The Associate Director reports to the Executive Director and is responsible for the daily planning, organizing, directing, and controlling of the daily operations, research and ...

Program Director, Clinical Research Informatics - Clinical Research
By Keck Medical Center of USC At , Los Angeles, 90015, Ca $158,080 - $260,832 a year
Program Planning and Management - Plans and develops CRI objectives and content. Identify trends and research needs and establish priorities accordingly.
Identify technical education opportunities to enhance user experience.
Develops and manages program budgets and recommends or makes budgetary and resource allocations. Provides financial status reports as requested.
Ensures all information systems products meet standards and user requirements. Tests software and hardware and monitors and resolves problems.
Advises leadership regarding Informatics systems requirements. Facilitates planning and directs the design, installation, modification, and operations of research information systems.
Reviews and prioritizes systems development requests. Prepares cost estimates for current and proposed projects, reflecting staff and equipment requirements.
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.
Associate Director / Director Clinical Operations
By CymaBay Therapeutics At Newark, CA, United States
Experience in line management of Clinical Operations team members
Identify risks to study timelines and propose mitigations and implement solutions with team and executive management support.
Strong program-level fiscal management and able to contribute to departmental budget
Ensure compliance with protocol, overall clinical objectives, and regulatory requirements.
Complete other responsibilities as needed and agreed upon.
Bachelor’s degree or equivalent training and experience (i.e., technical degree)
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
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 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 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 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 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 (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.
Associate Director, Clinical Qa (Archived)
By GXPeople At ,
BSc/BA, MSc or PhD and a minimum 10 years’ experience in Clinical QA.
Expert knowledge of relevant guidelines and regulations.
Experience working with CROs or other third-parties.
The desire to change / save the world then…
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
Associate Director, Research & Evaluation
By Jumpstart For Young Children Inc At , New York, 10018 $74,000 - $78,000 a year
People Management Skills: Experience managing direct reports.
Project Management Skills: Experience managing multiple projects or tasks under deadlines.
Data Skills: Ability to manage, analyze, and draw interpretations from large datasets in Microsoft Excel.
Partnership Skills: Experience working across departments, preferably within the context of empowering non-data people to embrace research and evaluation.
Knowledge of the Field of Education: Understanding of the education landscape, including early education, higher education, and workforce development
Knowledge of the Field of Education:
Director – Clinical Research, Skinceuticals Dmi
By L'Oréal At New York, NY, United States
Leads and develops contracts, Invoices, and Finances related to procedures and protocols for Global team for 7-10 projects.
Monitors and oversees study requirements are conducted, including ensuring the study inclusion/exclusion factors, products, time points, and panelists are included.
Advanced Clinical/Science degree or professional credentials required (BS, MS, PhD, PharmD, and/or scientific background/experience)
Rele ant transferable experience (clinical practice, clinical or scientific training, academic research, and regulatory/scientific).
Experience in Medical/Cosmetic Dermatology, Plastic Surgery, Cellular Biology, and/or Facial Aesthetic disciplines strongly desired.
Strong analytical skills and presentation skills
Clinical Research Associate (Cra)
By Peachtree BioResearch Solutions At Atlanta, GA, United States
Work closely with the Site Management team and sponsor stakeholders so you can plan and manage your work most effectively
Work with Peachtree's Data Management team and sites to ensure all queries are resolved
1-5 years of experience working on clinical trials (CRO or Sponsor) as either a coordinator or CRA I
Experience with CNS, rare disease and/or oncology studies preferred
Experience working in a CTMS and EDC system
Excellent organizational and critical thinking skills
Clinical Research Associate Jobs
By Candel Therapeutics At Needham, MA, United States
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 Lyra Therapeutics At Watertown, MA, United States

Lyra Therapeutics, Inc. is a clinical-stage biotechnology company developing novel, integrated drug and delivery solutions for the localized treatment of patients with chronic rhinosinusitis (CRS) ...

Clinical Research Associate (Cra)
By LumaBridge At United States
Ability to independently prioritize tasks with excellent time management skills.
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans.
Perform other duties as assigned by management.
Excellent verbal and written communication skills and conflict resolution abilities.
Oversee and conduct monitoring activities, including remote monitoring and risk-based monitoring.
Lead assigned sites through regular contact to ensure site compliance, adequate enrollment, and understanding of study requirements.