BioSpace, Inc.
Overview
Join to apply for the
Clinical Trial Manager #4356
role at
BioSpace . 4 days ago Be among the first 25 applicants. Our mission is to detect cancer early, when it can be cured. We are working to change the trajectory of cancer mortality and bring stakeholders together to adopt innovative, safe, and effective technologies that can transform cancer care. We are a healthcare company, pioneering new technologies to advance early cancer detection. We have built a multi-disciplinary organization of scientists, engineers, and physicians and we are using the power of next-generation sequencing (NGS), population-scale clinical studies, and state-of-the-art computer science and data science to overcome one of medicines greatest challenges. GRAIL is headquartered in Menlo Park, California, with locations in Washington, D.C., North Carolina, and the United Kingdom. It is supported by leading global investors and pharmaceutical, technology, and healthcare companies. For more information, please visit grail.com. Responsibilities Manages all clinical operational aspects of a clinical trial from site selection, start-up, enrollment, maintenance, and close-out Prepares and reviews study related plans and documents including protocols, informed consent forms, recruitment plans, monitoring plans, protocol deviation plans, and case report forms with minimal supervision Participates in identifying, selecting, and monitoring the performance of clinical sites Ensures proper site training and management, provides ongoing oversight of clinical site compliance with study plans, study protocol, SOPs, FDA regulations, ICH/GCP guidelines, and in accordance with all applicable regulations Participates in EDC set-up by contributing to case report form design, user acceptance testing, completion guideline development and other related activities Identifies any potential risks to the study timelines and/or conduct, proposes mitigations and implements mitigations with cross-functional team and manager support Monitors clinical data entry progress and follows up on incomplete data entry and/or outstanding queries Contributes to the development and management of site budgets and ensures invoice payment according to site payment terms Works cross functionally with other departments such as Legal, Clinical Data Management, Biospecimen Management, Finance, Clinical Compliance, Clinical Development, and Lab Operations on all aspects of the clinical trial Provides oversight of regional study monitors and/or contract research organizations (CRO) and facilitates external communication with site staff and pharmaceutical partners (as applicable) Ensures Trial Master File (TMF) is current and maintained; provides guidance and mentorship to CPAs (Clinical Project Assistants)
Preferred Qualifications
Bachelors degree or equivalent in the life sciences or related field required Additional coursework in clinical trial planning and execution is strongly desired At least 5+ years of relevant experience in managing clinical trials at a sponsor company (pharma, biotech, or medical device) with a strong track record of successful trial initiation and execution Industry experience within in vitro diagnostics (IVD) highly preferred; pharmaceutical, biologics or medical device experience also acceptable Thorough knowledge of GCP, ICH guidelines and other US and international clinical regulatory requirements Working experience with an electronic data capture system, CTMS system, and eTMF system Experience working on Investigational Device Exemption (IDE) and Real World Evidence (RWE) studies (highly preferred) Strong interpersonal communication (written and verbal), organizational and prioritization skills Able to work effectively under a fast-paced and changing environment Strong work ethic and demonstrated ability to deliver assignments on time Proficient with office automation tools, such as Microsoft Office and the Google suite of apps
The expected, full-time, annual base pay scale for this position is $117K - $138K for Menlo Park, CA. Actual base pay will consider skills, experience, and location. Based on the role, colleagues may be eligible to participate in an annual bonus plan tied to company and individual performance, or an incentive plan. We also offer a long-term incentive plan to align company and colleague success over time. In addition, GRAIL offers a progressive benefit package, including flexible time-off, a 401k with a company match, and alongside our medical, dental, vision plans, carefully selected mindfulness offerings. GRAIL is an Equal Employment Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status. We will reasonably accommodate all individuals with disabilities so that they can participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. GRAIL maintains a drug-free workplace. Expiry
IsExpired: false #J-18808-Ljbffr
Join to apply for the
Clinical Trial Manager #4356
role at
BioSpace . 4 days ago Be among the first 25 applicants. Our mission is to detect cancer early, when it can be cured. We are working to change the trajectory of cancer mortality and bring stakeholders together to adopt innovative, safe, and effective technologies that can transform cancer care. We are a healthcare company, pioneering new technologies to advance early cancer detection. We have built a multi-disciplinary organization of scientists, engineers, and physicians and we are using the power of next-generation sequencing (NGS), population-scale clinical studies, and state-of-the-art computer science and data science to overcome one of medicines greatest challenges. GRAIL is headquartered in Menlo Park, California, with locations in Washington, D.C., North Carolina, and the United Kingdom. It is supported by leading global investors and pharmaceutical, technology, and healthcare companies. For more information, please visit grail.com. Responsibilities Manages all clinical operational aspects of a clinical trial from site selection, start-up, enrollment, maintenance, and close-out Prepares and reviews study related plans and documents including protocols, informed consent forms, recruitment plans, monitoring plans, protocol deviation plans, and case report forms with minimal supervision Participates in identifying, selecting, and monitoring the performance of clinical sites Ensures proper site training and management, provides ongoing oversight of clinical site compliance with study plans, study protocol, SOPs, FDA regulations, ICH/GCP guidelines, and in accordance with all applicable regulations Participates in EDC set-up by contributing to case report form design, user acceptance testing, completion guideline development and other related activities Identifies any potential risks to the study timelines and/or conduct, proposes mitigations and implements mitigations with cross-functional team and manager support Monitors clinical data entry progress and follows up on incomplete data entry and/or outstanding queries Contributes to the development and management of site budgets and ensures invoice payment according to site payment terms Works cross functionally with other departments such as Legal, Clinical Data Management, Biospecimen Management, Finance, Clinical Compliance, Clinical Development, and Lab Operations on all aspects of the clinical trial Provides oversight of regional study monitors and/or contract research organizations (CRO) and facilitates external communication with site staff and pharmaceutical partners (as applicable) Ensures Trial Master File (TMF) is current and maintained; provides guidance and mentorship to CPAs (Clinical Project Assistants)
Preferred Qualifications
Bachelors degree or equivalent in the life sciences or related field required Additional coursework in clinical trial planning and execution is strongly desired At least 5+ years of relevant experience in managing clinical trials at a sponsor company (pharma, biotech, or medical device) with a strong track record of successful trial initiation and execution Industry experience within in vitro diagnostics (IVD) highly preferred; pharmaceutical, biologics or medical device experience also acceptable Thorough knowledge of GCP, ICH guidelines and other US and international clinical regulatory requirements Working experience with an electronic data capture system, CTMS system, and eTMF system Experience working on Investigational Device Exemption (IDE) and Real World Evidence (RWE) studies (highly preferred) Strong interpersonal communication (written and verbal), organizational and prioritization skills Able to work effectively under a fast-paced and changing environment Strong work ethic and demonstrated ability to deliver assignments on time Proficient with office automation tools, such as Microsoft Office and the Google suite of apps
The expected, full-time, annual base pay scale for this position is $117K - $138K for Menlo Park, CA. Actual base pay will consider skills, experience, and location. Based on the role, colleagues may be eligible to participate in an annual bonus plan tied to company and individual performance, or an incentive plan. We also offer a long-term incentive plan to align company and colleague success over time. In addition, GRAIL offers a progressive benefit package, including flexible time-off, a 401k with a company match, and alongside our medical, dental, vision plans, carefully selected mindfulness offerings. GRAIL is an Equal Employment Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status. We will reasonably accommodate all individuals with disabilities so that they can participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. GRAIL maintains a drug-free workplace. Expiry
IsExpired: false #J-18808-Ljbffr