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Remote Clinical Research Associate Jobs in Ohio

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
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
Ycci Clinical Research Associate (Monitor)
By Yale University At , New Haven, 06519, Ct
Preferred Education, Experience and Skills:
SOCRA/ACRP (or equivalent) certification; Master’s Degree or other advanced degree in related field.
YCCI Clinical Research Associate (Monitor)
None - Not included in the union (Yale Union Group)
Click here to see our Wage Ranges
Total # of hours to be worked:
Clinical Research Associate I
By TECHNICAL RESOURCES INT'L At , Bethesda, 20817, Md

: � Provides site management and monitoring support for sponsored clinical studies; primarily Phase I and II, with limited Phase III and IV. � Performs on-site pre-study/qualification, ...

Clinical Research Associate Jobs
By Battelle At Columbus, OH, United States
Supervise research data collection, management, and reporting
Support risk management activities both on projects and within the QS
Act as liaison between medical device design and manufacturing to assure transfer is smooth and responsibilities are managed and executed
Develop and implement forms and documentation to meet requirements of new studies with investigational medical devices
Lead test execution and conformance to requirements
Five years of specific experience as a Clinical Research Associate or equivalent for investigational medical devices.
Clinical Research Associate Jobs
By BioInforMedica At , West Chester, Pa

Positions range from junior to senior levels with regional opportunities in addition to in house positions. Responsibilities include conducting Phase I - IV single or multi center studies ...

Clinical Research Associate - Research Nurses
By Medpace, Inc. At , Cincinnati, 45227, Oh
Defined CRA promotion and growth ladder with potential for mentoring and management advancements
Must be detail-oriented and efficient in time management.
PACE® will prepare you by developing your CRA skills through interactive discussions and hands on job-related exercises and practicums.
Dynamic working environment, with varying responsibilities day-to-day
Expansive experience in multiple therapeutic areas
The opportunity to work from home;
Associate Director Clinical Business Process - Colorado Remote
By UnitedHealth Group At , Lakewood, 80123, Co $101,200 - $184,000 a year
Coach and develop management team to acquire and refine necessary job skills through constructive feedback, ongoing training, and other coaching techniques.
Facilitates process improvement working meetings with management team on a regular basis to discuss opportunities, issues, and action plans.
Coordination of staff activities and workflow in the areas of Documentation Management, Release of Information, Systems and MPI Integrity.
Manages relationships with market staff to ensure information is shared with providers for quality improvement.
Proven solid leadership and organizational skills and excellent communication skills
Assumes a leadership role in planning and implementation of programs and initiatives.

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