INSIGHTEC
Take your career to the next level as a
Clinical Project Manager
at
INSIGHTEC , a growing medical technology company transforming patient lives through innovative incisionless surgery.
Our culture is unique and diverse, driven by core values of Patients, Integrity, Team, Quality, and Innovation.
The Clinical Project Manager serves as the clinical trial lead and will lead clinical trial initiatives for Insightec. You will ensure trial compliance, regulatory alignment, and operational efficiency while collaborating with cross‑functional teams such as Medical Affairs, R&D, and Quality & Regulatory to advance Insightec’s clinical pipeline. The Clinical Project Manager is expected to independently manage the clinical trial by effectively planning and executing the study to ensure quality of deliverables within the specified budget and timeframe.
Key Responsibilities
Lead and manage multiple clinical trials from initiation through to completion, ensuring adherence to study timelines and budgets.
Collaborate with investigators, vendors, and cross‑functional teams to ensure study execution and operational excellence, including implementation of best practices such as quality by design.
Oversee the preparation and review of trial‑related documentation, including protocols, informed consent forms (ICFs), case report forms (CRFs), and clinical study reports.
Support creation of investigator brochures, clinical evaluation reports, publications and other documentation such as annual reports as applicable.
In partnership with R&D Program Management, develop and drive cross‑functional study timelines related to trial setup and execution.
Drive the cross‑functional internal study team ensuring appropriate alignment, risk management and coordination across all participating functions.
Interface with Data Management, Biostatistics and Clinical Monitors to ensure seamless monitoring and data cleaning initiatives to meet study deliverables and timelines.
Foster a collaborative team environment focused on operational efficiency and continuous improvement.
Regulatory and Compliance Oversight
Ensure that clinical trials are conducted in compliance with all applicable regulations and ISO 14155 and ICH‑GCP guidelines.
Lead submissions of clinical trial documents to central IRB/IECs as applicable and ensure insurance and recruitment materials are prepared appropriately.
Support the preparation and submission of clinical trial applications, including IDEs, PMAs, 501K, INDs, and other regulatory documents with functional leads from regulatory affairs.
Manage interactions with Regulatory Affairs and external vendors to ensure timely submissions and approvals.
Develop and manage clinical trial budgets, ensuring efficient use of resources and timely financial reporting.
Monitor and control trial costs to ensure alignment with project forecasts and company objectives.
Negotiate contracts and budgets with clinical vendors and investigators.
Vendor and Site Management
Oversee the selection and management of clinical research sites and clinical vendors (CROs, laboratories, etc.) and ensure they meet performance expectations.
Develop strong relationships with clinical sites and external partners to ensure aggressive site startup, high‑quality data collection, and trial conduct.
Perform risk assessment and management, addressing issues proactively to mitigate operational issues.
Qualifications
Bachelor's or Master's degree in life sciences or a related field.
7+ years of experience as a Clinical Project Manager for Class II/III device studies.
3+ years of regulatory/clinical trial experience in the medical device industry.
Demonstrates working knowledge of clinical trial design.
Minimum of three years of experience developing clinical documents including protocols, informed consent, clinical study reports, and investigator brochures.
Knowledge of financial principles in budgeting, budget negotiation, & contracts management.
Demonstrates data management skills, tracking study metrics, and adherence to study protocol.
Fluent in English with oral presentation and training capabilities.
Able and willing to travel as needed, up to 30%.
Expertise in GCP and regulatory requirements.
Strong leadership and team management skills.
Seniority Level
Associate
Employment Type
Full-time
Job Function
Research, Science, and Quality Assurance
Industries
Medical Device, Pharmaceutical Manufacturing, and Biotechnology Research
#J-18808-Ljbffr
Clinical Project Manager
at
INSIGHTEC , a growing medical technology company transforming patient lives through innovative incisionless surgery.
Our culture is unique and diverse, driven by core values of Patients, Integrity, Team, Quality, and Innovation.
The Clinical Project Manager serves as the clinical trial lead and will lead clinical trial initiatives for Insightec. You will ensure trial compliance, regulatory alignment, and operational efficiency while collaborating with cross‑functional teams such as Medical Affairs, R&D, and Quality & Regulatory to advance Insightec’s clinical pipeline. The Clinical Project Manager is expected to independently manage the clinical trial by effectively planning and executing the study to ensure quality of deliverables within the specified budget and timeframe.
Key Responsibilities
Lead and manage multiple clinical trials from initiation through to completion, ensuring adherence to study timelines and budgets.
Collaborate with investigators, vendors, and cross‑functional teams to ensure study execution and operational excellence, including implementation of best practices such as quality by design.
Oversee the preparation and review of trial‑related documentation, including protocols, informed consent forms (ICFs), case report forms (CRFs), and clinical study reports.
Support creation of investigator brochures, clinical evaluation reports, publications and other documentation such as annual reports as applicable.
In partnership with R&D Program Management, develop and drive cross‑functional study timelines related to trial setup and execution.
Drive the cross‑functional internal study team ensuring appropriate alignment, risk management and coordination across all participating functions.
Interface with Data Management, Biostatistics and Clinical Monitors to ensure seamless monitoring and data cleaning initiatives to meet study deliverables and timelines.
Foster a collaborative team environment focused on operational efficiency and continuous improvement.
Regulatory and Compliance Oversight
Ensure that clinical trials are conducted in compliance with all applicable regulations and ISO 14155 and ICH‑GCP guidelines.
Lead submissions of clinical trial documents to central IRB/IECs as applicable and ensure insurance and recruitment materials are prepared appropriately.
Support the preparation and submission of clinical trial applications, including IDEs, PMAs, 501K, INDs, and other regulatory documents with functional leads from regulatory affairs.
Manage interactions with Regulatory Affairs and external vendors to ensure timely submissions and approvals.
Develop and manage clinical trial budgets, ensuring efficient use of resources and timely financial reporting.
Monitor and control trial costs to ensure alignment with project forecasts and company objectives.
Negotiate contracts and budgets with clinical vendors and investigators.
Vendor and Site Management
Oversee the selection and management of clinical research sites and clinical vendors (CROs, laboratories, etc.) and ensure they meet performance expectations.
Develop strong relationships with clinical sites and external partners to ensure aggressive site startup, high‑quality data collection, and trial conduct.
Perform risk assessment and management, addressing issues proactively to mitigate operational issues.
Qualifications
Bachelor's or Master's degree in life sciences or a related field.
7+ years of experience as a Clinical Project Manager for Class II/III device studies.
3+ years of regulatory/clinical trial experience in the medical device industry.
Demonstrates working knowledge of clinical trial design.
Minimum of three years of experience developing clinical documents including protocols, informed consent, clinical study reports, and investigator brochures.
Knowledge of financial principles in budgeting, budget negotiation, & contracts management.
Demonstrates data management skills, tracking study metrics, and adherence to study protocol.
Fluent in English with oral presentation and training capabilities.
Able and willing to travel as needed, up to 30%.
Expertise in GCP and regulatory requirements.
Strong leadership and team management skills.
Seniority Level
Associate
Employment Type
Full-time
Job Function
Research, Science, and Quality Assurance
Industries
Medical Device, Pharmaceutical Manufacturing, and Biotechnology Research
#J-18808-Ljbffr