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 challenging and rewarding career in clinical research? We are looking for a Clinical Research Associate to join our team and help us develop and execute clinical studies. You will be responsible for managing clinical trials, ensuring compliance with applicable regulations, and providing support to investigators and sponsors. If you have a passion for clinical research and want to make a difference, this is the job for you!

Overview:

A Clinical Research Associate (CRA) is a healthcare professional who works in clinical research and is responsible for monitoring the progress of clinical trials. The CRA is responsible for ensuring that clinical trials are conducted in accordance with the protocol, applicable regulations, and ethical standards.

Detailed Job Description:

A Clinical Research Associate is responsible for the planning, coordination, and execution of clinical trials. This includes the development of study protocols, the selection of clinical sites, the recruitment of study participants, the collection and analysis of data, and the reporting of results. The CRA is also responsible for ensuring that the clinical trial is conducted in accordance with the protocol, applicable regulations, and ethical standards.

What is Clinical Research Associate Job Skills Required?

• Knowledge of clinical research principles, regulations, and guidelines
• Excellent organizational and communication skills
• Ability to work independently and as part of a team
• Ability to manage multiple tasks and prioritize work
• Attention to detail and accuracy
• Proficiency in Microsoft Office applications

What is Clinical Research Associate Job Qualifications?

• Bachelor’s degree in a related field
• Previous experience in clinical research or related field
• Certification as a Clinical Research Associate (CCRA) or Clinical Research Professional (CRCP)

What is Clinical Research Associate Job Knowledge?

• Knowledge of clinical research principles, regulations, and guidelines
• Knowledge of Good Clinical Practice (GCP)
• Knowledge of medical terminology
• Knowledge of clinical trial design and data analysis

What is Clinical Research Associate Job Experience?

• Previous experience in clinical research or related field
• Experience in monitoring clinical trials
• Experience in data collection and analysis

What is Clinical Research Associate Job Responsibilities?

• Develop and implement clinical trial protocols
• Monitor clinical trial sites to ensure compliance with protocol and applicable regulations
• Recruit and screen study participants
• Collect and analyze data
• Prepare and submit reports to regulatory agencies
• Maintain accurate and up-to-date records
• Ensure the safety of study participants