Senior Clinical Scientist
Jobs via Dice, Raleigh, NC, United States
We are looking for a highly motivated Senior Clinical Scientist to support global clinical development programs. This role involves contributing to clinical strategy, study design, execution, and data interpretation to support regulatory approvals and product development initiatives.
This is a contract opportunity with potential for extension or full-time conversion. Candidates interested in permanent roles should be open to relocating to Raleigh, NC within a defined timeframe.
Key Responsibilities
Provide scientific and strategic input across all stages of clinical development
Support clinical trial design, execution, and data analysis
Collaborate with cross-functional and global teams
Author and review clinical documents (protocols, reports, investigator brochures, etc.)
Interpret clinical data and provide meaningful insights
Contribute to regulatory documentation and submissions
Prepare and present clinical trial results to stakeholders
Support publications including manuscripts, abstracts, and posters
Manage and oversee external medical writing vendors
Ensure compliance with regulatory guidelines (FDA, EMA, ICH-Google Cloud Platform, ISO)
Required Skills
Strong scientific writing and communication skills
Knowledge of clinical trials and clinical development processes
Familiarity with FDA/EMA regulations, ICH-Google Cloud Platform, and ISO standards
Ability to manage multiple projects and priorities effectively
Strong analytical, problem-solving, and collaboration skills
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This is a contract opportunity with potential for extension or full-time conversion. Candidates interested in permanent roles should be open to relocating to Raleigh, NC within a defined timeframe.
Key Responsibilities
Provide scientific and strategic input across all stages of clinical development
Support clinical trial design, execution, and data analysis
Collaborate with cross-functional and global teams
Author and review clinical documents (protocols, reports, investigator brochures, etc.)
Interpret clinical data and provide meaningful insights
Contribute to regulatory documentation and submissions
Prepare and present clinical trial results to stakeholders
Support publications including manuscripts, abstracts, and posters
Manage and oversee external medical writing vendors
Ensure compliance with regulatory guidelines (FDA, EMA, ICH-Google Cloud Platform, ISO)
Required Skills
Strong scientific writing and communication skills
Knowledge of clinical trials and clinical development processes
Familiarity with FDA/EMA regulations, ICH-Google Cloud Platform, and ISO standards
Ability to manage multiple projects and priorities effectively
Strong analytical, problem-solving, and collaboration skills
#J-18808-Ljbffr