Opportunity
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. The incumbent will collaborate closely with the medical monitor, operations team, CRO partner, and study sites to ensure efficient recruitment and follow‐up of subjects in accordance with study protocols. Reporting to the VP, Clinical Development, the Senior Clinical Scientist will be responsible for the compilation and analysis of study data for various internal and external reports, as well as key meetings.
Key Responsibilities
* Trial Design and Execution: participate in protocol development, develop study CRFs, ICFs and databases
* Data Analyses and Monitoring: monitor clinical trial data for accuracy and integrity
* Compliance: ensure all study activities adhere to regulatory and ethical guidelines
* Collaboration: act as a bridge between medical monitor, operations, CRO and study sites to ensure efficient communication, subject recruitment and trial management
* Reports: write study reports, plans, and make data presentations for internal and external meetings
* Other duties as assigned
Required Qualifications
* 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
Preferred 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
* Demonstrated success in leading cross‐functional teams and managing external partners (CROs)
* Strong collaborator with strategic planning and independent problem‐solving skills
* Experienced in patient safety guidelines
* Knowledgeable about clinical trial ethics and regulatory standards
* Strong follow‐up skills
* 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
* 401(k) with company matching
$142,000 - $178,000 a year
It is our policy and intent to provide equal opportunity to all persons without regard to race, color, religion, political affiliation, sex/gender (including gender expression/identity, pregnancy, childbirth and related medical conditions), marital status, registered domestic partner status, sexual orientation, age, ancestry, national origin, veteran status, disability, medical condition, genetic characteristics, and/or any other basis protected by law. This policy covers all facets of employment including, but not limited to: recruitment, selection, placement, promotions, transfers, demotions, terminations, training, and compensation.
Mammoth Biosciences requires that all employees be vaccinated against COVID as a condition of at‐will employment, with exceptions for medical or religious reasons in compliance with local, state, and federal law.
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