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Phase 1 Scientist Jobs in Idaho

Forensic Scientist 1 (Fs1) Jobs
By Amentum At , Dover
Minimum Education and Experience Requirements:
Supporting the logistical or resource management activities of the DNA Registry
Accessioning forensic evidence in the Laboratory Information Management System (LISA).
Participating in the organization and presentation of educational activities.
Possess strong written and verbal communication skills
Assisting in program maintenance and development at the direction of their designated supervisor.
Forensic Scientist 1 Evidence Custodian
By Amentum At , Dover, De
Minimum Education and Experience Requirements:
Supporting the logistical or resource management activities of the DNA Registry
Accessioning forensic evidence in the Laboratory Information Management System (LISA)
Participating in the organization and presentation of educational activities
A Bachelor’s degree or Associate’s degree with two years of experience in forensic science or in physical or life sciences
General knowledge of forensic DNA analytical methods
Forensic Scientist 1 (Fs1) Jobs
By Amentum At , Dover, De
Minimum Education and Experience Requirements:
Supporting the logistical or resource management activities of the DNA Registry
Accessioning forensic evidence in the Laboratory Information Management System (LISA).
Participating in the organization and presentation of educational activities.
Possess strong written and verbal communication skills
Assisting in program maintenance and development at the direction of their designated supervisor.

Are you a scientist looking for a new challenge? We are looking for a Phase 1 Scientist to join our team and help us develop innovative solutions to complex problems. You will have the opportunity to work with cutting-edge technology and collaborate with a diverse team of experts. If you are passionate about science and have a creative approach to problem-solving, this could be the perfect role for you!

Overview A Phase 1 Scientist is a research scientist who is responsible for conducting clinical trials in the early stages of drug development. They are responsible for designing, executing, and analyzing clinical trials to assess the safety and efficacy of new drugs. They are also responsible for ensuring that all regulatory requirements are met. Detailed Job Description A Phase 1 Scientist is responsible for designing, executing, and analyzing clinical trials in the early stages of drug development. They must ensure that all regulatory requirements are met, and that the clinical trials are conducted in accordance with Good Clinical Practice (GCP) guidelines. They must also ensure that the data collected is accurate and reliable. The Phase 1 Scientist is responsible for preparing and submitting regulatory documents, such as Investigational New Drug (IND) applications, to the appropriate regulatory agencies. They must also ensure that all safety and efficacy data is collected and reported in a timely manner. Job Skills Required
• Knowledge of clinical trial design and execution
• Knowledge of Good Clinical Practice (GCP) guidelines
• Knowledge of regulatory requirements
• Excellent communication and interpersonal skills
• Strong organizational and problem-solving skills
• Ability to work independently and as part of a team
• Ability to work under pressure and meet deadlines
Job Qualifications
• Bachelor’s degree in a scientific field
• At least 5 years of experience in clinical research
• Knowledge of clinical trial design and execution
• Knowledge of Good Clinical Practice (GCP) guidelines
• Knowledge of regulatory requirements
• Excellent communication and interpersonal skills
Job Knowledge
• Knowledge of clinical trial design and execution
• Knowledge of Good Clinical Practice (GCP) guidelines
• Knowledge of regulatory requirements
• Knowledge of data analysis and interpretation
• Knowledge of medical terminology
Job Experience
• At least 5 years of experience in clinical research
• Experience in designing, executing, and analyzing clinical trials
• Experience in preparing and submitting regulatory documents
• Experience in data analysis and interpretation
Job Responsibilities
• Design, execute, and analyze clinical trials
• Ensure that all regulatory requirements are met
• Prepare and submit regulatory documents
• Collect and report safety and efficacy data
• Analyze and interpret data
• Monitor clinical trial progress and report any issues
• Ensure that all clinical trials are conducted in accordance with GCP guidelines