COMPANY MISSION
eGenesis is dedicated to giving patients with organ failure a second chance at life by harnessing the power of genome engineering to create safe effective and readily available solutions.
eGenesis is seeking a resourceful and collaborative Senior Clinical Trial Manager to join our Clinical
Operations team to support programs across our portfolio. This role will work closely with our teams
across Regulatory Quality GMP Production and Development to successfully drive our clinical
programs. As the Senior Clinical Trial Manager you will be responsible for the day-to-day management
of our clinical studies vendors and sites in alignment with corporate and program goals. You will work
closely with clinical sites and CROs to ensure compliance with SOPs and regulatory guidelines. To be
successful in this role you will leverage a passion for the details excellent communication skills and an
eagerness to collaborate.
PRIMARY RESPONSIBILITIES
- Manage all aspects of clinical trials including study vendor management CRO oversight timelines and budgets
- Assist in preparation and review of clinical study documentation including but not limited to protocol informed consent Clinical Monitoring Plan Project Plan Case Report Forms Clinical Study Reports and other study level documents
- Engage cross-functionally to ensure clear consistent communication to key stakeholders on study status metrics and timelines
- Ensure implementation and conduct of study(ies) in accordance with SOPs and ICH-GCP guidelines
- Serve as point of contact for CRO and clinical site communication
- Set up the Trial Master File (TMF) and appropriately maintain the TMF throughout the trial including periodic reviews
- Participate and coordinate resolution of audit findings and ensure audit-ready condition of clinical trial documentation including central clinical files
- Proactively identify risks in study timelines in regard to key milestones and deliverables and work closely with the cross-functional teams to mitigate downstream impacts
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:
Manager
COMPANY MISSIONeGenesis is dedicated to giving patients with organ failure a second chance at life by harnessing the power of genome engineering to create safe effective and readily available solutions.eGenesis is seeking a resourceful and collaborative Senior Clinical Trial Manager to join our Clin...
COMPANY MISSION
eGenesis is dedicated to giving patients with organ failure a second chance at life by harnessing the power of genome engineering to create safe effective and readily available solutions.
eGenesis is seeking a resourceful and collaborative Senior Clinical Trial Manager to join our Clinical
Operations team to support programs across our portfolio. This role will work closely with our teams
across Regulatory Quality GMP Production and Development to successfully drive our clinical
programs. As the Senior Clinical Trial Manager you will be responsible for the day-to-day management
of our clinical studies vendors and sites in alignment with corporate and program goals. You will work
closely with clinical sites and CROs to ensure compliance with SOPs and regulatory guidelines. To be
successful in this role you will leverage a passion for the details excellent communication skills and an
eagerness to collaborate.
PRIMARY RESPONSIBILITIES
- Manage all aspects of clinical trials including study vendor management CRO oversight timelines and budgets
- Assist in preparation and review of clinical study documentation including but not limited to protocol informed consent Clinical Monitoring Plan Project Plan Case Report Forms Clinical Study Reports and other study level documents
- Engage cross-functionally to ensure clear consistent communication to key stakeholders on study status metrics and timelines
- Ensure implementation and conduct of study(ies) in accordance with SOPs and ICH-GCP guidelines
- Serve as point of contact for CRO and clinical site communication
- Set up the Trial Master File (TMF) and appropriately maintain the TMF throughout the trial including periodic reviews
- Participate and coordinate resolution of audit findings and ensure audit-ready condition of clinical trial documentation including central clinical files
- Proactively identify risks in study timelines in regard to key milestones and deliverables and work closely with the cross-functional teams to mitigate downstream impacts
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:
Manager
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