Register
Recruit Create CV

Remote Clinical Research Associate Jobs in Texas

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 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 Baylor College of Medicine At , Houston, 77030, Tx
Two years of relevant experience.
Supports daily operations for a research study or clinical trial.
Recruits, screens, and enrolls study participants; ensures participant adherence to study protocol.
Collects, evaluates, enters, and tracks data.
Submits data, study documents, and/or reports to regulatory agencies.
Assists with completion of protocol-specific documents.
Associate Clinical Research Iii
By Abbott Laboratories At , Seattle, Wa $71,300 - $142,700 a year
Participates in adverse event reporting and safety responsibilities monitoring.
May participate in adverse event reporting and safety responsibilities monitoring.
Knowledge of regulations governing medical devices is desirable.
Career development with an international company where you can grow the career you dream of.
Free medical coverage for employees* via the Health Investment Plan (HIP) PPO
An excellent retirement savings plan with high employer contribution
Clinical Research Associate - Research Nurse Experience
By Medpace At Irving, TX, United States
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;

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