Septerna
Sr. Clinical Trial Manager
Septerna, South San Francisco, California, us, 94083
Septerna is a biotechnology company based in South San Francisco, CA on a mission to develop life-changing medicines for patients with the vision to become the industry-leading G protein-coupled receptor (GPCR)-focused drug discovery company. The company's Native Complex Platform™ recapitulates GPCRs with their native structure, function, and dynamics outside of the cellular context. This approach enables novel access to modern structural and screening technologies used in industrial-scale drug discovery for the entire class of GPCRs. Septerna has an emerging pipeline of GPCR-targeted small molecule programs with potential for growth to target many GPCRs that have been undruggable and unexploited to date.
We are excited to expand our multidisciplinary team of individuals focused on creating revolutionary medicines to address the unmet needs of patients. At Septerna we strive to embrace diversity of thought, expertise, and background through collaboration. To join our ambitious team, be prepared to bring your real self to work every day; grow and learn from a talented team of drug hunters, scientists, and business professionals; and contribute your passion, creativity, and energy to accomplish our mission. We share a fearless pursuit of ground-breaking innovations and cultivate an environment where our employees succeed by learning from each other and working as a team.
We are committed to the development of meaningful therapeutics for patients with indications of high unmet need. This is a tremendous opportunity to work with talented individuals on the frontlines of therapeutic discovery and development. You will directly help move therapies through preclinical research, positioning them for success in the clinic. The successful candidate will add their passion, unique talents, and expertise to a dynamic team motivated to discover new disease-modifying therapeutics for patients in a fast-paced environment.
For more information see: www.septerna.com.
About The Role This position will provide clinical trial management support for ongoing and future clinical trials in our lead program. Candidate will function as the Clinical Trial Lead across several studies that is managed in-house by the Septerna Clinical Operations Team. Partnering closely with the cross-functional stakeholders (Clinical, Regulatory, Product Development), you will apply strong clinical and project management fundamentals for the implementation of various aspects of our clinical trials. The Clinical Trial Manager (CTM) will play a key role in the planning, execution, and management of clinical trials. This includes overseeing the operational aspects of the trials from start-up through close-out, ensuring trials are conducted in compliance with GxP regulations, company policies, and standard operating procedures (SOPs)
Essential Functions
Sr. Clinical Trial Manager will be responsible for managing various aspects of clinical trial conduct with internal cross functional team members involving clinical development, contract vendors, and regulatory to achieve clinical trial goals on time and within budgetDevelop internal tracking and reporting tools for reporting study status to Leadership and facilitate internal clinical study team meetingsCo-development and management (review, revision, tracking and filing) of study materials, including but not limited to:Protocols, regulatory submissions, informed consent, site budgets and agreements, training materials, newsletters, presentations for various stakeholdersDeveloping (or overseeing the development of) all training/day to day materials, including SIV materials, Investigator Meeting materials, Amendment Training Materials, and any other trial-specific trainingsLeadership of assigned meetings (cross-functional (internal), vendor, and/or investigator) and provision of regular updates on study status, e.g., agenda development, minutes curation and filingCollaborate with Data Management Vendor to develop/review eCRF and completion guidelines as well as conduct user acceptance testing prior to release.Oversee data entry timelines and query management, including metric reporting.Participate in site monitoring visits as necessaryProvide oversight and management of regional CRO assigned Clinical Research Associates (CRAs) including review of site visit reports and training records.Contribute to the development and refinement of clinical trial processes and procedures.Develop and maintain (or oversee) the development of the Trial Master File, ensuring the final TMF is final and audit ready at the close of the studyParticipate and support all audit, SOP and quality activities, the vendors, the sites, etc. to ensure alignment and consistent quality exist across the trialFacilitate and manage productive team communication and collaboration, both internally and externally.Qualifications
The ideal candidate should have a minimum of a bachelor's degree in the life sciences and 5-8 years of direct and progressive experience specific to biotech clinical trial management with a track record of successful management of complex programs using multiple external vendors.Global clinical trial management strongly preferred"Early-stage clinical trial experience is a plus, but not a prerequisiteStrong working knowledge of ICH-GCP guidelines, FDA regulations, and international regulatory requirementsHigh attention to detail.; ability to manage multiple projects simultaneously.Build and preserve relationships with colleague's investigator site staffs and clinical trial partnersCandidates should have experience with Microsoft office programs and web-based data entry platforms.Candidates should have a passion for learning, creating, relating, communicating, and helping drive the success of cross functional teams.Ability to travel to clinical sites as needed.
The anticipated salary range for candidates who will work in South San Francisco, CA is $185,000 - $205,000. Individual pay may vary based on additional factors, including, and without limitation, job-related skills, experience, work location and relevant education or training. Septerna's compensation package also includes benefits, stock options, and annual target bonus for full-time positions.
Note to Employment Agencies: Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited. We are an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. Septerna participates in the E-Verify program. California Consumer Privacy Act Privacy Notice For Job Applicants. If you are a California resident, click here for our CCPA Notice.
We are excited to expand our multidisciplinary team of individuals focused on creating revolutionary medicines to address the unmet needs of patients. At Septerna we strive to embrace diversity of thought, expertise, and background through collaboration. To join our ambitious team, be prepared to bring your real self to work every day; grow and learn from a talented team of drug hunters, scientists, and business professionals; and contribute your passion, creativity, and energy to accomplish our mission. We share a fearless pursuit of ground-breaking innovations and cultivate an environment where our employees succeed by learning from each other and working as a team.
We are committed to the development of meaningful therapeutics for patients with indications of high unmet need. This is a tremendous opportunity to work with talented individuals on the frontlines of therapeutic discovery and development. You will directly help move therapies through preclinical research, positioning them for success in the clinic. The successful candidate will add their passion, unique talents, and expertise to a dynamic team motivated to discover new disease-modifying therapeutics for patients in a fast-paced environment.
For more information see: www.septerna.com.
About The Role This position will provide clinical trial management support for ongoing and future clinical trials in our lead program. Candidate will function as the Clinical Trial Lead across several studies that is managed in-house by the Septerna Clinical Operations Team. Partnering closely with the cross-functional stakeholders (Clinical, Regulatory, Product Development), you will apply strong clinical and project management fundamentals for the implementation of various aspects of our clinical trials. The Clinical Trial Manager (CTM) will play a key role in the planning, execution, and management of clinical trials. This includes overseeing the operational aspects of the trials from start-up through close-out, ensuring trials are conducted in compliance with GxP regulations, company policies, and standard operating procedures (SOPs)
Essential Functions
Sr. Clinical Trial Manager will be responsible for managing various aspects of clinical trial conduct with internal cross functional team members involving clinical development, contract vendors, and regulatory to achieve clinical trial goals on time and within budgetDevelop internal tracking and reporting tools for reporting study status to Leadership and facilitate internal clinical study team meetingsCo-development and management (review, revision, tracking and filing) of study materials, including but not limited to:Protocols, regulatory submissions, informed consent, site budgets and agreements, training materials, newsletters, presentations for various stakeholdersDeveloping (or overseeing the development of) all training/day to day materials, including SIV materials, Investigator Meeting materials, Amendment Training Materials, and any other trial-specific trainingsLeadership of assigned meetings (cross-functional (internal), vendor, and/or investigator) and provision of regular updates on study status, e.g., agenda development, minutes curation and filingCollaborate with Data Management Vendor to develop/review eCRF and completion guidelines as well as conduct user acceptance testing prior to release.Oversee data entry timelines and query management, including metric reporting.Participate in site monitoring visits as necessaryProvide oversight and management of regional CRO assigned Clinical Research Associates (CRAs) including review of site visit reports and training records.Contribute to the development and refinement of clinical trial processes and procedures.Develop and maintain (or oversee) the development of the Trial Master File, ensuring the final TMF is final and audit ready at the close of the studyParticipate and support all audit, SOP and quality activities, the vendors, the sites, etc. to ensure alignment and consistent quality exist across the trialFacilitate and manage productive team communication and collaboration, both internally and externally.Qualifications
The ideal candidate should have a minimum of a bachelor's degree in the life sciences and 5-8 years of direct and progressive experience specific to biotech clinical trial management with a track record of successful management of complex programs using multiple external vendors.Global clinical trial management strongly preferred"Early-stage clinical trial experience is a plus, but not a prerequisiteStrong working knowledge of ICH-GCP guidelines, FDA regulations, and international regulatory requirementsHigh attention to detail.; ability to manage multiple projects simultaneously.Build and preserve relationships with colleague's investigator site staffs and clinical trial partnersCandidates should have experience with Microsoft office programs and web-based data entry platforms.Candidates should have a passion for learning, creating, relating, communicating, and helping drive the success of cross functional teams.Ability to travel to clinical sites as needed.
The anticipated salary range for candidates who will work in South San Francisco, CA is $185,000 - $205,000. Individual pay may vary based on additional factors, including, and without limitation, job-related skills, experience, work location and relevant education or training. Septerna's compensation package also includes benefits, stock options, and annual target bonus for full-time positions.
Note to Employment Agencies: Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited. We are an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. Septerna participates in the E-Verify program. California Consumer Privacy Act Privacy Notice For Job Applicants. If you are a California resident, click here for our CCPA Notice.