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Clinical Research Coordinator Associate Jobs

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 Coordinator Jobs
By Rady Children's Hospital-San Diego At San Diego County, CA, United States

Job Summary: Initiates & manages multiple cooperative group trials such as Children's Oncology Group (COG) clinical trials related to pediatric cancer to include, but not limited to: execution ...

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 Coordinator Jobs
By Duke University At , Durham, 27710
May develop resources and tools for management of international studies, and/or coordinate with other entities or offices.
Proactively seeks opportunities to add relevant skills and certifications to own portfolio.
Knowledgeable in regulatory and institutional policies and processes; applies appropriately in study documentation, protocol submissions, and SOPs.
Develops data entry or collection SOPs or tools.
Recognizes and reports security of physical and electronic data vulnerabilities.
Uses required EMR functionalities to manage participants and study visits.
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 Coordinator Jobs
By Mayo Clinic At , Scottsdale, 85259 $29.39 - $44.09 an hour

Graduate or diploma from a study coordinator training program is preferred. Medical terminology course preferred.

Affirmative Action and Equal Opportunity Employer

Dps Clinical Research Coordinator
By City of Hope At Duarte, CA, United States
Bachelor’s Degree or Certified CRA or Certified Tumor Registrar in lieu of degree. Experience may substitute for minimum education requirements.
Basic education, experience and skills required for consideration:
Preferred education, experience and skills:
Conducts protocol database management for an assigned set of multiple research protocols.
Makes recommendations and participates in Policy and Procedure development regarding particular areas of team assignment and general data management issues.
Identifies and communicates important protocol and data management issues or problem areas to supervisor.
Clinical Research Coordinator Jobs
By Northwell Health At , Lake Success, 11020 $58,540 - $92,650 a year
Bachelor's Degree required, or equivalent combination of education and related experience.
Collects labels, logs, processes, and ships biological specimens for analysis according to protocol and training requirements.
1-3 years of relevant experience, required.
Responsible for coordination of a designated study or group of studies.
In research projects, oversees recruitment of subjects, implementation of study procedures, and the collection and processing of data.
Keeps accurate and up-to-date records.
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)
Associate Clinical Research Coordinator - Cbru
By Mayo Clinic At , Jacksonville, 32224 $22.91 - $33.27 an hour
Preference given to candidates with the following qualifications:
Sincere interest in promoting research within local underrepresented communities.
Affirmative Action and Equal Opportunity Employer
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 Coordinator Jobs
By Phoenix Children's Hospital At , Phoenix
Creates study budgets and works with management to determine financial feasibility and resources necessary to conduct the trial
Reviews all regulatory requirements to ensure implementation of appropriate methods, practices, and procedures for all research activities in designated area
With the principal investigator, explains the study purpose, parameters, and requirements of the studies to the participants
Completes case report forms, data entry, and maintains source documentation for all study participants
Offering the most comprehensive care across ages, communities and specialties
Advancing education and training to shape the next generation of clinical leaders
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 Coordinator Jobs
By Hospital for Special Surgery At , New York, 10021
2 years experience in Clinical Research is preferred
Proficient use of computers and software Working of knowledge of Microsoft Excel is strongly desired; Word, PowerPoint, EDC, EMR (preferably EPIC)
Knowledge of Orthopaedic and/or Rheumatologic terminology is a plus.
Working of knowledge of Microsoft
Recruitment process (conducts informed consent process)
The development and build of Clinical Research Forms
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 Coordinator Ii
By Sutter Health At , Palo Alto $40.85 - $61.28 an hour
Mentors and fosters a constructive teaching environment that helps students and new teammates build confidence in their skills, knowledge and abilities.
Performs information management functions, including maintaining databases, entering and auditing data, may perform trending.
Ensures compliance with protocol guidelines and requirements of regulatory agencies.
2 years experience conducting clinical research.
2 years experience ensuring compliance with research regulations.
Equivalent experience will be accepted in lieu of the required degree or diploma.
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 Coordinator Jobs
By The University of Pittsburgh At , Pittsburgh
Will this position accept substitution in lieu of education or experience?
Minimum Years of Experience Required
Med-Medicine - Pennsylvania-Pittsburgh - (23005905)
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.