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Remote Clinical Research Associate Jobs

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 Associate - Mid-West/Central - Cns/Gen Med - Home Based
By Worldwide Clinical Trials At United States
Excellent interpersonal, oral, and written communication skills in English
Superior organizational skills with attention to details
5+ years of experience as a Clinical Research Associate
Experience in CNS is required
Conduct study initiation visits (SIVs)
Ability to work with little or no supervision
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.
Associate Clinical Research Monitor (Remote) Thv
By Edwards Lifesciences At , $64,000 - $91,000 a year
Excellent written and verbal communication skills, presentation skills, interpersonal skills, and analytical skills are required
Good problem-solving and critical thinking skills
Understanding of medical device regulatory requirements and documents, device accountability and adverse events reporting
Technical writing skills (protocols, CRF development, study tools)
Good computer skills in MS Office Suite, including Word, Excel, Adobe, and ability to operate general computer software and office machinery
Experience with electronic data capture preferred
Manager, Clinical Research Administration (Remote)
By WCG At , Madison $97,200 - $136,000 a year
Attend trainings to ensure growth in general management techniques and company‐specific knowledge, as required.
Opportunities for career development with on-the-job training, certification assistance, and continuing education reimbursement
Display integrity and positive attitude when dealing with employees, management, and clients.
Volunteer Time Off to benefit the community
Must have a bachelor’s degree from an accredited college or university, or an associate degree (AA) with equivalent work experience.
Experience in providing exceptional customer service in a fast paced, proactive, results-driven, and dynamic environment.
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
Research Associate (Remote Or Hybrid) ($76200.00 - $110400.00 / Year)
By Talentify.io At United States
Excellent writing, presentation, project management, and interpersonal skills required
BA degree in Finance, Statistics, or Economics preferred
Industry experience in quantitative risk modeling and/or loss forecasting preferred
Strong analytical background and programming skills (Ex: Stata, SQL, R, Matlab, C++, Python) considered
Reasonable accommodation provided for qualified individuals with disabilities or religious beliefs
Develop, implement, and validate credit models using statistical and econometric techniques
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
Research Associate - Remote | Wfh
By Get It Recruit - Educational Services At Boston, MA, United States

Are you ready to embark on a journey of intellectual curiosity and creative exploration? We're on the lookout for a passionate and driven individual who thrives in a collaborative, high-energy ...

Clinical Research Monitor (Remote) Tmtt
By Edwards Lifesciences At Albuquerque-Santa Fe Metropolitan Area, United States
3 years of previous clinical research field monitoring experience OR, quality assurance/control and regulatory compliance experience, required
Experience working in a medical device or regulated industry, preferred
Experience with electronic data capture, preferred
Excellent written and verbal communication skills, presentation skills, interpersonal skills, and analytical skills are required
Demonstrated problem-solving and critical thinking skills
Understanding of medical device regulatory requirements and documents, device accountability and adverse events reporting
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.
Research Associate- Early Education- Remote ($68325.00 - $116152.00 / Year)
By Talentify.io At United States
Excellent task management and organizational skills
Experience with data collection and data management in applied settings
Experience with different meeting platforms, content management systems, and data systems
Collaborate with colleagues to develop analytic plans and data management procedures
Strong critical thinking skills and problem-solving abilities
Gain experience working on multiple early childhood projects simultaneously
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.

Are you looking for a unique opportunity to make a difference in the healthcare industry? We are seeking a Remote Clinical Research Associate to join our team and help us develop innovative treatments for patients. You will be responsible for monitoring clinical trials, ensuring compliance with protocols, and providing support to investigators and sponsors. If you have a passion for clinical research and want to make a real impact, this is the job for you!

Overview A Remote Clinical Research Associate (CRA) is a professional who is responsible for the management and coordination of clinical trials. The CRA is responsible for ensuring that the clinical trial is conducted in accordance with the protocol, applicable regulations, and Good Clinical Practices (GCP). The CRA is also responsible for monitoring the progress of the clinical trial, ensuring that the data collected is accurate and complete, and reporting any adverse events or other issues to the sponsor. Detailed Job Description

The Remote Clinical Research Associate is responsible for the management and coordination of clinical trials. This includes:

• Developing and maintaining relationships with clinical sites and investigators
• Ensuring that the clinical trial is conducted in accordance with the protocol, applicable regulations, and Good Clinical Practices (GCP)
• Monitoring the progress of the clinical trial
• Ensuring that the data collected is accurate and complete
• Reporting any adverse events or other issues to the sponsor
• Assisting in the preparation of regulatory documents
• Assisting in the preparation of clinical study reports
• Assisting in the preparation of data for submission to regulatory authorities
• Assisting in the preparation of presentations for investigators and other stakeholders
• Assisting in the preparation of training materials for investigators and other stakeholders
• Assisting in the preparation of budgets and contracts
• Assisting in the preparation of study materials
• Assisting in the preparation of study protocols
• Assisting in the preparation of informed consent forms
• Assisting in the preparation of study reports
• Assisting in the preparation of study databases
• Assisting in the preparation of study manuals
• Assisting in the preparation of study monitoring plans
• Assisting in the preparation of study closure documents
Job Skills Required
• Excellent communication skills
• Strong organizational skills
• Ability to work independently and as part of a team
• Ability to manage multiple tasks and prioritize workload
• Knowledge of clinical trial regulations and Good Clinical Practices (GCP)
• Knowledge of clinical trial processes and procedures
• Knowledge of clinical trial data management
• Knowledge of clinical trial software
• Knowledge of medical terminology
• Knowledge of medical devices
• Knowledge of clinical research terminology
Job Qualifications
• Bachelor’s degree in a related field
• At least two years of experience in clinical research
• Certification as a Clinical Research Associate (CRA)
Job Knowledge
• Knowledge of clinical trial regulations and