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Apex Clinical Research Associate Jobs

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.
Clinical Research Associate I, Dcri
By Duke University At , Durham, 27710
Review education and training experience with line manager and complete identified training needs within designated time period.
*Basic knowledge of site management and clinical monitoring for clinical research studies
Maintain job knowledge and skills through independent self-study.
OR EQUIVALENT COMBINATION OF EDUCATION AND EXPERIENCE
None required beyond that described above. OR AN EQUIVALENT COMBINATION OF RELEVANT EDUCATION AND/OR EXPERIENCE
Perform assessment of site personnel and facilities for study conduct through feasibility and site telephone qualification
Clinical Research Associate Ii - Phoenix / Tucson
By ICON At , Phoenix
Knowledge of ICH and local regulatory authority regulations regarding drug
Experience in monitoring all trial components (PSSV to COV)
Ability to travel as needed (greater than 40%)
Associate Clinical Research Coordinator
By Mayo Clinic At , Scottsdale, 85259 $24.75 - $36.69 an hour

Affirmative Action and Equal Opportunity Employer

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 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.
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.
Associate Clinical Research Associate (Remote -West Region)
By Merck Sharp & Dohme At , Rahway, 07065, Nj $72,880 - $114,600 a year
Developing skills in Site Management including management of site performance and patient recruitment
Effective time management, organizational and interpersonal skills, conflict management
Able to work with other experienced research professions to develop skills across multiple protocols, sites and therapy areas.
Coordinates & manages various tasks in collaboration with other sponsor roles to achieve Site Ready.
Manages and maintains information and documentation in CTMS, eTMF and various other systems as appropriate and per timelines.
Good understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines.
Clinical Research Associate, Sponsor Dedicated
By IQVIA At , Remote
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
2 years of clinical research coordinator experience strongly preferred
While projects vary, your typical responsibilities might include:
We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe
Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
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 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) ...

Research Associate, Clinical Biomarker Laboratory, Virus Neutralization Assays & Bio-Analytics
By Moderna At Norwood, MA, United States
Identify and resolve quality issues and report issues to upper management
Good computational skills, preferably experienced with Word, Excel, Power Point, GraphPad Prism
Conduct assay development, qualification/validation and sample analysis on a variety of platforms (ELISA, MSD, Ella, Automated ELISA Workstation etc.)
Assume assigned general laboratory responsibilities, e.g., safety coordinator, instrument/process/technology owner etc.
Bachelor or MSc in bioanalysis or related field with immunoassay experience preferably in a regulated environment
Good written, presentation, and interpersonal communication skills
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 (Usa)
By Premier Research At , Remote
4+ years of independent on-site monitoring experience with all types of site visits
We are Built by You. Your ideas influence the way we work, and your voice matters here
Identify and escalate potential risks and possible retraining opportunities for investigative sites.
Bachelor’s degree, or local equivalent, in a clinical, biological, scientific, or health-related field or its international equivalent
Completion of a CRA training program through a CRO
You must live in United States
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.
Clinical Research Associate Jobs
By WEP Clinical At Raleigh-Durham-Chapel Hill Area, United States
High organizational and logistics skills to ensure effective management of multiple sites and protocols within timeframes and on budget
Approximately 2-5 years of on-site and remote monitoring experience
Broad range of therapeutic experience
Superior written and verbal communication skills
Wren Nursing (Clinical Trial Home Nursing & Clinical Education)
Contribute to the development of protocols, study tools, materials, and documentation for clinical sites.
Clinical Research Associate Jobs
By ProTrials Research, Inc. At , $85,000 - $120,000 a year
Bachelor and/or advanced degree in biological sciences or related field, or equivalent combination of relevant experience, education or training
Managing and training of site personnel on therapeutic area, protocol requirements, proper source documentation, and case report form completion
Excellent organizational skills, strong interpersonal and communications skills, and strong problem-solving skills
Extensive knowledge of FDA regulations and their practical implementation
2 years of prior experience as a Clinical Research Associate preferred
Full medical, dental, and vision benefit packages
Clinical Research Associate-208919 Jobs
By Medix™ At Florida, United States

The CRA is expected to work cooperatively with study team and operations management to proactively drive project success.

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