Senior Clinical Scientist

About the role

Mammoth Biosciences seeks an experienced Senior Clinical Scientist to advance pre-clinical research into clinical trials. This role encompasses both tactical and strategic responsibilities, including the design and execution of clinical trials, as well as meticulous monitoring of data for accuracy and integrity to ensure regulatory compliance.

Responsibilities

• participate in protocol development
• develop study CRFs, ICFs and databases
• monitor clinical trial data for accuracy and integrity
• ensure all study activities adhere to regulatory and ethical guidelines
• collaborate with the medical monitor, operations team, CRO partner, and study sites to ensure efficient communications, subject recruitment and trial management
• write study reports, plans, and make data presentations for internal and external meetings

Requirements

• Master’s degree/PharmD/PhD in a relevant life science field
• Minimum of 5 years experience in the pharmaceutical or biotechnology industry, with at least 2 years experience in clinical science/clinical development
• Demonstrated experience in the design, execution, and reporting of global Phase 1-3 clinical trials
• Strong proficiency in data analysis, interpretation of clinical trial results, and presenting data
• Deep knowledge of Good Clinical Practice (GCP), ICH guidelines, and global regulatory requirements for clinical trials (FDA, EMA, etc.)
• Excellent verbal, written, and presentation skills with proven ability to communicate with multiple stakeholders
• Ability to travel internationally for site visits as needed

Qualifications

• Experience managing or directly overseeing clinical monitoring and data management processes
• Prior experience in a clinical scientist role within a high-growth, fast-paced biotechnology environment
• Strategic planning and independent problem-solving skills
• Experienced in patient safety guidelines
• Knowledgeable about clinical trial ethics and regulatory standards
• Strong follow-up skills

Skills

• Strong proficiency in data analysis, interpretation of clinical trial results, and presenting data
• Deep knowledge of Good Clinical Practice (GCP), ICH guidelines, and global regulatory requirements for clinical trials (FDA, EMA, etc.)
• Excellent verbal, written, and presentation skills with proven ability to communicate with multiple stakeholders
• Ability to manage multiple conflicting priorities

Benefits

• Company-paid health/vision/dental benefits
• Unlimited vacation and generous sick time
• Company-sponsored meals and snacks
• Wellness, caregiver and ergonomics benefits
• $142,000 - $178,000 a year actual base salary will be determined by relevant professional experience, applicable skills, and internal equity

Pay

$142,000 - $178,000 a year

Schedule

Actual schedule will be determined by relevant professional experience, applicable skills, and internal equity.