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Corbus Pharmaceuticals
Norwood, MA, United States
Company Description Corbus Culture: Our passion. Our purpose. At Corbus, it starts at our core. We look for unique talent. Our people are brilliant, they break barriers and are not defined by a title. Eclectic experiences make Corbus a special place to share ideas and grow. At Corbus, transformative ideas can come from anyone, anywhere and anyti
Job Source: Corbus PharmaceuticalsConfidential
Boston, MA, United States
Director, Clinical Operations About the Company Esteemed clinic facility Industry Hospital & Health Care Type Privately Held About the Role The Director, Clinical Operations will be responsible for overseeing operational planning activities, collaborating with cross functional teams, and managing and resolve study conduct issues. Travel Percent 2
Job Source: ConfidentialActalent
Boston, MA, United States
Job Title: Director Clinical Operations (ONCOLOGY) Job Description As a Director of Clinical Operations (Oncology) - you will be accountable for the operational planning and execution of First-in-Human, clinical pharmacology patient studies, and Phases 1-3 clinical trials (primarily phase III) This role includes responsibility for clinical program
Job Source: ActalentMonte Rosa Therapeutics, Inc
Boston, MA, United States
Overview: Monte Rosa Therapeutics is seeking a highly experienced Clinical Operations professional to lead the successful planning, implementation, and conduct of clinical trials across multiple indications. Reporting to the Head of Clinical Operations, the Director, Clinical Operations will be responsible and accountable for development of operat
Job Source: Monte Rosa Therapeutics, IncMonte Rosa Therapeutics, Inc
Boston, MA, United States
Overview: Monte Rosa Therapeutics is seeking a highly experienced Clinical Operations professional to lead the successful planning, implementation, and conduct of clinical trials across multiple indications. Reporting to the Head of Clinical Operations, the Director, Clinical Operations will be responsible and accountable for development of operat
Job Source: Monte Rosa Therapeutics, IncVor Biopharma Inc.
Cambridge, MA, United States
Who we are looking for: Vor Bio is seeking a highly motivated Director, Clinical Operations to join our fast-paced, dynamic team at this exciting phase of our Clinical Development Program. Key areas of responsibility: * Executes the day-to-day operations of clinical trials from the protocol concept through the clinical study report, per established
Job Source: Vor Biopharma Inc.Corbus Pharmaceuticals
Norwood, MA, United States
We are seeking a Director, Clinical Operations to provide strategic leadership and operational planning expertise to Corbus Pharmaceuticals clinical development programs. We are looking for an experienced Clinical Program Manager who can lead the creation and high-quality implementation of thoughtful clinical develop plans. This position is both a
Job Source: Corbus PharmaceuticalsSchrödinger Inc.
Cambridge, MA, United States
Schrödinger is revolutionizing drug discovery through the use of breakthrough computational methods that are advancing internal programs into the clinic. We’re seeking a Director/Senior Director of Clinical Operations to join the New York-based Early Clinical Development team. This hire will oversee study management activities, budgets, and c
Job Source: Schrödinger Inc.Norwood, MA, United States
We are seeking a Director, Clinical Operations to provide strategic leadership and operational planning expertise to Corbus Pharmaceuticals clinical development programs. We are looking for an experienced Clinical Program Manager who can lead the creation and high-quality implementation of thoughtful clinical develop plans. This position is both a member of the Core Team and an integral co-leader responsible for the effective operations of the Clinical Sub-team, facilitating cross-functional engagement both internally and with vendor partners as part of a fully outsourced operating model.
Ideally this role will be located in Norwood, Massachusetts as a hybrid role 3 days onsite weekly.
Responsibilities:
Providing operational expertise and strategic input to the development of Clinical Development Plans (CDP) supporting the overall clinical strategy for assigned clinical program(s); may lead some trial management activities within assigned program as well.
Providing program-level sponsor oversight of CRO and 3rd party vendors to ensure the effective execution of the clinical studies on time, with high quality (e.g., inspection ready) and within agreed budget.
Collaborating with cross-functional counterparts to oversee the performance for all activities assigned to our CROs and vendors, including escalation of issues when necessary.
Clinical program budget planning and external spend related to clinical program execution. Working closely with CROs and vendors, Program Management and Finance to ensure that budgets, enrollment, and forecasts are accurate.
Reviewing and providing expert clinical operations input into clinical documents including Investigator Brochures, Investigational New Drug Applications (INDs) and/or Investigational Medicinal Product Dossier (IMPDs), study synopsis and protocols, clinical study reports, applicable sections of the New Drug Application (NDA) and/or Marketing Authorization Application (MAA), updates to IND and NDA documents, DSURs and other safety reports; may be responsible for the management of clinical document creation or updates.
Providing expert clinical operations input into preparation for key regulatory meetings (e.g. End-of-Phase 2, Request for Scientific Advice Meetings, etc.), as appropriate.
Functional leadership which may include line management, providing input for issue resolution and leading and/or support functional strategic initiatives and process improvement.
Knowledge and Skills:
Bachelors Degree or international equivalent required, Life Sciences preferred.
10+ years experience in pharmaceutical industry and/or clinical research organization, including clinical study/project management/clinical trial management.
Experience of managing clinical programs through phase 1-4.
Metabolic or obesity trial experience
Thorough knowledge of FDA and ICH GCP guidelines to ensure the appropriate conduct of clinical studies globally
Extensive experience managing complex protocols, CROs, budgets, and timelines
Experience monitoring clinical studies and conducting SQVs, SIVs, IMVs, and COVs preferred
Expertise in global regulatory and compliance requirements for clinical research, including but not limited to US CFR, EU CTD, and ICH GCP.
Ability to competently manage multiple competing priorities, adapting as needs change. Must be comfortable working in a fast-paced environment.
Demonstrated excellence in program management, including scenario assessment, risk assessment, budget management, and contingency planning
Excellent teamwork, organizational, interpersonal, conflict resolution and problem-solving skills
Strong communication skills and ability to work with cross-functional study teams
Strong organizational skills, sufficient to multi-task in a fast-paced environment with changing priorities
Excellent written and oral communication skills, including the ability to effectively communicate statistical concepts in a clear and concise manner.
Ability to work independently and act with initiative to address issues
Corbus Culture:
Corbus is a close-knit team of high-achieving, innovative, creative and, above all else, passionate employees. We hire for personality as well as for skill. At Corbus, we take pride in our “family” atmosphere where each person’s contribution is vital to our success. As a Corbus employee, you are empowered to think creatively and be proactive in your approach. There is no place for politics or red tape here.
About Corbus:
Corbus is committed to leveraging our expertise in immunology to fulfill our purpose of developing innovative new medicines that improve the lives of people living with inflammatory, fibrotic, and metabolic diseases, and cancer. Corbus’ current pipeline includes small molecules that activate or inhibit the endocannabinoid system and anti-integrin monoclonal antibodies that block activation of TGFβ. Corbus is headquartered in Norwood, Massachusetts. For more information on Corbus, visit corbuspharma.com. Connect with us on Twitter, LinkedIn and Facebook.
Corbus Pharmaceuticals Holdings, Inc. is an equal opportunity employer
Email Alert for Director, Clinical Operations jobs in Norwood, MA, United States
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