Register
Recruit Create CV

Junior Clinical Trials Data Specialist Jobs in New Jersey

Clinical Trials Specialist Jobs
By Vitalief Inc. At New Brunswick, NJ, United States
Needs to be communicative and responsive and know when to escalate and communicate issues to management.
Oncology clinical research experience is required.
Any experience working with solid tumors is a big plus.
Demonstrated computer skills with Microsoft Office applications.
Vitalief is offering a $3,500 sign-on bonus for this position!
You'll impact clinical research in various therapeutic areas, including oncology, and improve outcomes for diverse populations.
Clinical Trials Specialist (Multiple Vacancies)
By Rutgers University At New Brunswick, NJ, United States
Equivalent education, experience and/or training may be substituted for the educational requirement.
Minimum of three (3) years of clinical research experience.
At least one (1) year of oncology experience.
Bilingual skills (English/Spanish); speaking, reading, and writing.
Collaborates with Protocol Activation office to initiate and activate all new clinical trial protocols assigned utilizing Oncore Study-start up task list.
Serves as an essential link between patients and all other members of the research team.
Clinical Trials Disclosure Specialist
By Synectics Inc. At New Jersey, United States
Project and stakeholder management experience
US military experience will be considered towards industry experience requirements
2-3 years of document redaction and 5 years relevant work experience in a scientific or medical field with BA/BS
Exceptional written and oral communication skills
Strong organizational skills with the ability to multitask and prioritize
BA/BS or MA/MS in scientific or medical field

Are you looking for an exciting opportunity to join a fast-paced clinical trials team? We are looking for a Junior Clinical Trials Data Specialist to join our team and help us manage and analyze data from clinical trials. This is a great opportunity to gain experience in a fast-growing field and make a real impact on patient care. If you're ready to take on a challenge and make a difference, apply now!

Overview A Junior Clinical Trials Data Specialist is responsible for collecting, organizing, and analyzing clinical trial data. They are responsible for ensuring that all data is accurate and up-to-date, and that it meets the standards of the clinical trial. They also provide support to clinical trial teams and other stakeholders in the clinical trial process. Detailed Job Description A Junior Clinical Trials Data Specialist is responsible for collecting, organizing, and analyzing clinical trial data. They are responsible for ensuring that all data is accurate and up-to-date, and that it meets the standards of the clinical trial. They also provide support to clinical trial teams and other stakeholders in the clinical trial process. This includes creating and maintaining databases, preparing reports, and providing technical assistance. They must also be able to identify and resolve data discrepancies. Job Skills Required
• Knowledge of clinical trial processes and regulations
• Proficiency in data analysis and interpretation
• Ability to work with large datasets
• Excellent organizational and communication skills
• Attention to detail
• Ability to work independently and as part of a team
• Knowledge of database management systems
Job Qualifications
• Bachelor’s degree in a related field
• Experience in clinical trials data management
• Knowledge of clinical trial processes and regulations
• Proficiency in data analysis and interpretation
• Ability to work with large datasets
• Excellent organizational and communication skills
• Attention to detail
• Ability to work independently and as part of a team
• Knowledge of database management systems
Job Knowledge
• Knowledge of clinical trial processes and regulations
• Knowledge of database management systems
• Knowledge of data analysis and interpretation
• Knowledge of clinical trial data management
Job Experience
• Experience in clinical trials data management
• Experience in data analysis and interpretation
• Experience in database management systems
• Experience in working with large datasets
Job Responsibilities
• Collect, organize, and analyze clinical trial data
• Ensure accuracy and up-to-date data
• Create and maintain databases
• Prepare reports
• Provide technical assistance
• Identify and resolve data discrepancies
• Support clinical trial teams and other stakeholders in the clinical trial process