CAN Canada
Associate Clinical Lead Director (Oncology)
CAN Canada, New York, New York, us, 10261
The
Associate Clinical Lead Director
provides leadership to the global Oncology clinical team, in support of the project leader, and in collaboration with the other functional teams, to achieve the delivery of the project’s overall objectives to the Sponsor’s satisfaction per contract while optimizing speed, quality and cost of delivery and in accordance with our SOPs, policies and practices.RESPONSIBILITIESAccountable for ensuring the “right subjects” and “right data” to meet our contractual requirements.May contribute to the development of the project delivery strategy for Request for Proposals (RFPs).Participate in bid defense preparations. Lead the Clinical delivery strategy at bid defense presentations in partnership with Project Leader Business Development for large, complex, multi-region studies. Understand the overall project strategy and translate the agreed upon clinical approach to a successful practical delivery model.Develop and maintain clinical project plans, including but not limited to clinical operations plan, recruitment and retention strategy plan, etc. to be incorporated into the integrated study management plan/project management plan.Accountable for the clinical delivery (subject recruitment, site management, data integrity) per contract, ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures.Partner with the project leaders to confirm objectives of the clinical team according to agreed-upon contract, strategy and approach. Effectively communicate and assess performance against these agreed objectives.Ensure all appropriate subject/patient recruitment strategies are in place at the outset of the study to maximize subject/patient recruitment opportunities to achieve delivery according to contract, including, but not limited to, all outreach or digital offerings being explored and deployed.Ensure all processes and tools are available to maximize clinical team’s ability to monitor and secure patient recruitment to the monitoring team from the outset of the study including, but not limited to a clear recruitment strategy plan, the subject/patient pathway materials and clearly defined contingency plans with agreed trigger points for deployment. Throughout the study these strategies and materials should be kept under constant review and updated in response to progress on the study to ensure clear understanding by all parties (internal and external) of expectations throughout the recruitment period; and inspire customer confidence in a clear and enforced action plan and thereby ensure successful delivery to customer satisfaction.Monitor clinical progress against contract and prepare/present project information proactively to all stakeholders internally and externally as required.Deliver the project/program according to the quality management plan. Guide CRAs and advise on critical specific study issues.Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles.Manage risks (positive and negative) which could impact on the clinical delivery of the project and determine contingencies.Partner with functional leaders in problem solving and resolution efforts.Achieve project quality by identifying quality risks and issues, responding to issues which impact the clinical delivery, responding to issues raised by project team members and planning/implementing appropriate corrective and preventative action plans.Serve as clinical project contact with customer where applicable and agreed with the project leader.Drive for high performance and efficiency of the clinical team to support financial success of the project.Support the project leader in ensuring the financial success of the project.Collaborate with the project leader in forecasting and identifying opportunities to accelerate activities to bring Site Management revenue forward. Ability to assess impact of project events which will have impact on financial performance.Participate in, champion and adopt function and/or corporate initiatives, changes and/or special project assignments; act as a client liaison, departmental cross-functional liaison and/or change agent.This is an Individual Contributor (IC) opportunity, meaning you will have no direct reports. However, our ACLDs provide input to line managers regarding their project team members’ performance relative to project tasks, support staff development, and mentor less experienced project team members on assigned projects to support their professional development.MINIMUM REQUIRED EDUCATION AND EXPERIENCEBachelor's degree in a health care or other scientific discipline with 10 years clinical research/monitoring experience; or equivalent combination of education, training and experience.At least 5-7 years of experience in a global Senior CL (Clinical Lead) / CTM (Clinical Trial Manager)/ CTL (Clinical Trial Lead)/ COL (Clinical Operations Lead) role, overseeing global trials / trial portfolios / clinical trial operations, with the majority of your experience focused in Oncology trials.Clinical Leadership at IQVIA…Clinical Leadership is focused on the delivery and quality of the contracted Clinical services within a project to achieve customer satisfaction. Focus is on leveraging clinical operations and therapeutic expertise along with the diverse IQVIA solutions to drive operational excellence particularly in respect to subject/patient recruitment and on time high quality data collection.This is a remote/WFH opportunityIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.comWe are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoeIQVIA’s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding COVID-19 vaccination status. https://jobs.iqvia.com/covid-19-vaccine-statusThe potential base pay range for this role, when annualized, is $123,200.00 - $228,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
Associate Clinical Lead Director
provides leadership to the global Oncology clinical team, in support of the project leader, and in collaboration with the other functional teams, to achieve the delivery of the project’s overall objectives to the Sponsor’s satisfaction per contract while optimizing speed, quality and cost of delivery and in accordance with our SOPs, policies and practices.RESPONSIBILITIESAccountable for ensuring the “right subjects” and “right data” to meet our contractual requirements.May contribute to the development of the project delivery strategy for Request for Proposals (RFPs).Participate in bid defense preparations. Lead the Clinical delivery strategy at bid defense presentations in partnership with Project Leader Business Development for large, complex, multi-region studies. Understand the overall project strategy and translate the agreed upon clinical approach to a successful practical delivery model.Develop and maintain clinical project plans, including but not limited to clinical operations plan, recruitment and retention strategy plan, etc. to be incorporated into the integrated study management plan/project management plan.Accountable for the clinical delivery (subject recruitment, site management, data integrity) per contract, ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures.Partner with the project leaders to confirm objectives of the clinical team according to agreed-upon contract, strategy and approach. Effectively communicate and assess performance against these agreed objectives.Ensure all appropriate subject/patient recruitment strategies are in place at the outset of the study to maximize subject/patient recruitment opportunities to achieve delivery according to contract, including, but not limited to, all outreach or digital offerings being explored and deployed.Ensure all processes and tools are available to maximize clinical team’s ability to monitor and secure patient recruitment to the monitoring team from the outset of the study including, but not limited to a clear recruitment strategy plan, the subject/patient pathway materials and clearly defined contingency plans with agreed trigger points for deployment. Throughout the study these strategies and materials should be kept under constant review and updated in response to progress on the study to ensure clear understanding by all parties (internal and external) of expectations throughout the recruitment period; and inspire customer confidence in a clear and enforced action plan and thereby ensure successful delivery to customer satisfaction.Monitor clinical progress against contract and prepare/present project information proactively to all stakeholders internally and externally as required.Deliver the project/program according to the quality management plan. Guide CRAs and advise on critical specific study issues.Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles.Manage risks (positive and negative) which could impact on the clinical delivery of the project and determine contingencies.Partner with functional leaders in problem solving and resolution efforts.Achieve project quality by identifying quality risks and issues, responding to issues which impact the clinical delivery, responding to issues raised by project team members and planning/implementing appropriate corrective and preventative action plans.Serve as clinical project contact with customer where applicable and agreed with the project leader.Drive for high performance and efficiency of the clinical team to support financial success of the project.Support the project leader in ensuring the financial success of the project.Collaborate with the project leader in forecasting and identifying opportunities to accelerate activities to bring Site Management revenue forward. Ability to assess impact of project events which will have impact on financial performance.Participate in, champion and adopt function and/or corporate initiatives, changes and/or special project assignments; act as a client liaison, departmental cross-functional liaison and/or change agent.This is an Individual Contributor (IC) opportunity, meaning you will have no direct reports. However, our ACLDs provide input to line managers regarding their project team members’ performance relative to project tasks, support staff development, and mentor less experienced project team members on assigned projects to support their professional development.MINIMUM REQUIRED EDUCATION AND EXPERIENCEBachelor's degree in a health care or other scientific discipline with 10 years clinical research/monitoring experience; or equivalent combination of education, training and experience.At least 5-7 years of experience in a global Senior CL (Clinical Lead) / CTM (Clinical Trial Manager)/ CTL (Clinical Trial Lead)/ COL (Clinical Operations Lead) role, overseeing global trials / trial portfolios / clinical trial operations, with the majority of your experience focused in Oncology trials.Clinical Leadership at IQVIA…Clinical Leadership is focused on the delivery and quality of the contracted Clinical services within a project to achieve customer satisfaction. Focus is on leveraging clinical operations and therapeutic expertise along with the diverse IQVIA solutions to drive operational excellence particularly in respect to subject/patient recruitment and on time high quality data collection.This is a remote/WFH opportunityIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.comWe are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoeIQVIA’s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding COVID-19 vaccination status. https://jobs.iqvia.com/covid-19-vaccine-statusThe potential base pay range for this role, when annualized, is $123,200.00 - $228,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.