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Remote Clinical Research Associate Jobs in Pennsylvania

Clinical Research Associate Jobs
By Juno Search Partners At Greater Philadelphia, United States
Able to manage multiple and competing priorities through effective organizational management skills.
Effective interpersonal skills; able to build effective relationships with study management team colleagues and business partners.
Excellent time management skills; able to accomplish established goals efficiently.
Supply chain management support may include:
Support Trial Management team member with assigned study specific projects and tasks.
Two years Clinical Research work experience, or relevant experience
Clinical Research Associate（Fsp Model）
By 北京博纳西亚医药科技有限公司（Panacea Technology Co.,Ltd.） At Pennsylvania, United States
Pre-Study/Start up Site Management Activities
Verify storage and shipment of biological samples and other protocol specific diagnostics requirement
At least 3-5 years clinical operation monitor experience for senior position.
Good knowledge in GCP for senior position
Good communication and organization skills
Identify potential sites, investigators and site staff;
Senior Clinical Research Associate
By Hydrogen Group At Philadelphia, PA, United States
Help provide oversight of clinical studies (site selection, study site initiation, provide daily communication and updates , document management, timeline management)
Provide administrative support for senior management
Conduct and/or assist teammates with on-site visits, including qualifications through close-outs; training clinical sites on implementation and conduct of study protocols
Solid tumor experience is a plus
Soft skills- attention to detail is a must, Sr VP/Head of clinical will 100% verify all reports
Monitor study progress, identify issues, and implement corrective actions as necessary.
Research Associate, Analytical Sciences And Clinical Testing Services
By Krystal Biotech, Inc. At Pittsburgh, PA, United States
Background knowledge/experience of GMP, GLP, GCP, USP, and/or ICH requirements is a plus
Performs other duties as assigned by manager
2+ years of experience in aseptic cell culture is required
Experience with molecular and cell-based assays including ELISA, Real Time qPCR, and Western Blotting is strongly desired
Experience in virology or gene therapy is desired including titer assays
Excellent oral and written communication skills required

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