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 an 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 for 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 communications 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
Masters 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
$142000 - $178000 a year
Actual base salary will be determined by relevant professional experience applicable skills and internal equity.
COMPANY
Mammoth Biosciences is a biotechnology company focused on leveraging its proprietary ultracompact CRISPR systems to develop long-term curative therapies as well as other applications such as decentralized precision diagnostics. Founded by CRISPR pioneer and Nobel laureate Jennifer Doudna and Trevor Martin Janice Chen and Lucas Harrington the companys ultracompact proteins are designed to enable in vivo gene editing in difficult to reach tissues utilizing both nuclease applications and new editing modalities beyond double stranded breaks including base editing gene writing and epigenetic editing. The company is building out its pipeline of potential in vivo gene editing therapeutics and capabilities and has partnerships with leading pharmaceutical and biotechnology companies to broaden the reach of its innovative and proprietary technology. Mammoths deep science and industry experience along with a robust and differentiated intellectual property portfolio have enabled the company to further its mission to transform the lives of patients and deliver on the full promise of CRISPR technologies.
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.
We may use artificial intelligence (AI) tools to support parts of the hiring process such as reviewing applications analyzing resumes or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed please contact us.
Required Experience:
Senior IC
OPPORTUNITYMammoth 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 a...
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 an 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 for 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 communications 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
Masters 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
$142000 - $178000 a year
Actual base salary will be determined by relevant professional experience applicable skills and internal equity.
COMPANY
Mammoth Biosciences is a biotechnology company focused on leveraging its proprietary ultracompact CRISPR systems to develop long-term curative therapies as well as other applications such as decentralized precision diagnostics. Founded by CRISPR pioneer and Nobel laureate Jennifer Doudna and Trevor Martin Janice Chen and Lucas Harrington the companys ultracompact proteins are designed to enable in vivo gene editing in difficult to reach tissues utilizing both nuclease applications and new editing modalities beyond double stranded breaks including base editing gene writing and epigenetic editing. The company is building out its pipeline of potential in vivo gene editing therapeutics and capabilities and has partnerships with leading pharmaceutical and biotechnology companies to broaden the reach of its innovative and proprietary technology. Mammoths deep science and industry experience along with a robust and differentiated intellectual property portfolio have enabled the company to further its mission to transform the lives of patients and deliver on the full promise of CRISPR technologies.
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.
We may use artificial intelligence (AI) tools to support parts of the hiring process such as reviewing applications analyzing resumes or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed please contact us.
Required Experience:
Senior IC
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14 hours ago
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