Associate Decentralized Clinical Trial Lead
hace 2 días
Associate Decentralized Clinical Trial Study Lead (aDCTL) / Decentralized Clinical Trial Lead (DCTL) are an integral part of clinical trial delivery to improve patients' lives and bring therapies to the market faster. The aDCTL / DCTL roles requires strong project management skills, customer and site facing engagement experience, creativity/innovation and the ability to thrive in a dynamic setting.
The aDCTL / DCTL may oversee studies ranging from fully decentralized trials to hybrid studies which require liaising with traditional project delivery teams. Critical to the success of DCT is the ability to collaborate across multiple teams and stakeholders including but not limited to technology & IT , mobile nursing, site support services, regulatory, site startup, etc. aDCTL / DCTL's also follow established SOP and policies focused on project delivery, productivity and quality resulting in strong project financial performance and customer satisfaction.
Essential Functions
- Accountable for the strategic development and delivery of DCT studies in line with agreed upon contracts while optimizing speed, quality and cost of delivery, ensuring consistent use of study tools and training materials and compliance with system updates, standard processes, policies and procedures.
- Serve as DCT project oversight and/or contact with customers and own relationship with the project's key customer contact(s)
- Set objectives and manage for the DCT project team according to agreed upon contract, strategy and approach for operational delivery, effectively communicate and assess performance, providing feedback and leadership.
- Collaborate with other functional groups within the company where necessary, including the core study team, to develop and/or support the preparation of integrated study management plans, support milestone achievement and manage study issues and obstacles.
- Monitor progress against contract and prepare/present project information proactively to all stakeholders internally and externally.
- Supervise Foresee problem solving and resolution efforts to include management of risks, and manage contingencies and issues. Take accountability for proactive contingency plans to mitigate risks.
- Achieve project quality by identifying and proactively managing quality risks and issues, responding to issues raised by project team members and /implementing appropriate corrective and preventative action plans.
Take ownership, understand the budget and drive optimal project financial management from initial load to study closeout
- Ensure the financial success of the project including optimal management and assignment of resources to achieve project goals and profitability.
- Actively work on preserving DCT scope and Forecast and identify opportunities to accelerate activities to bring milestones and revenue forward and implement appropriate actions to achieve.
- Identify changes in scope and manage change control process, including securing customer agreement to financial and milestone updates as necessary.
- Identify and communicate lessons learned and best practices to promote continuous improvement.
Other Functions May Include
- Participate in bid defense preparations. Lead bid defense presentations in partnership with Business Development for 100% Virtual studies or as a component of the larger team for integrated hybrid DCTs studies. Understand project strategy and operationalize the agreed upon approach.
- Adopt corporate initiatives and changes and serve as a change advocate when necessary.
- Provide input to line managers on their project team members' performance relative to project tasks. Support staff development. Mentor less experienced project team members on assigned projects to support their professional development.
- Educate and train other teams and partners on the processes, capabilities and structure of the DCT organization.
- Communicate/collaborate with IQVIA business development representatives as necessary.
- May participate in executive committees as part of program leadership.
Qualifications
- Bachelor's Degree Life sciences or related field
- Requires +4 years relevant clinical research experience plus around 3 years of experience in project management experience.
- Requires advanced knowledge of and experience implementing Project Management methodologies, ideally within the clinical research space.
- Broad knowledge of DCT (current challenges and opportunities to improve clinical trial delivery) and other related job areas, typically obtained through advanced education combined with experience.
- Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct.
- Technology Savvy – You have an affinity for learning and leveraging technology. Prior experience with set up or implementation of new platform/systems is a plus.
- Communication - Strong written and verbal communication skills including good command of English language. Strong presentation, negotiation and customer management skills.
- Finances - Good understanding of project financials including experience managing financials (budget), contractual obligations and implications.
IQVIA 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
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
-
Clinical Trial Associate
hace 3 semanas
Mexico City ICON A tiempo completoClinical Trial Associate, Shanghai, office base ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Clinical Trial...
-
Clinical Trial Associate
hace 3 semanas
Mexico City ICON A tiempo completoClinical Trial Associate, Shanghai, office base ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Clinical Trial...
-
Clinical Trial Manager I, Biotech
hace 2 días
Mexico City Metropolitan Area IQVIA A tiempo completoIQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure, collaborative culture, and deep therapeutic expertise allow us to deliver tailored solutions that help bring innovative treatments to patients faster.Job OverviewAssociate Clinical Leads...
-
Remote Clinical Trial Delivery Manager
hace 2 semanas
Mexico City ICON Clinical Research A tiempo completoA leading clinical research organization is seeking a Clinical Trial Manager based in Mexico. The successful candidate will oversee the planning, execution, and completion of clinical trials, ensuring adherence to standards and compliance with regulations. Collaborating with cross-functional teams and managing site relationships is key to this role....
-
Clinical Trial Manager
hace 2 días
Mexico City Metropolitan Area IQVIA A tiempo completoJob OverviewClinical Trial Manager are an integral part of clinical trial delivery, working alongside clinical teams to improve patients' lives by bringing new drugs to the market faster. The Clinical Trial manager is a member of the core project team responsible for the clinical delivery of clinical studies to meet contractual requirements in accordance...
-
Clinical Trial Associate
hace 2 días
Mexico City ICON Strategic Solutions A tiempo completoMexico City. Office based. ICON plc is a world‑leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. What You Will Be Doing Assist in the coordination and administration...
-
Senior Clinical Supply Lead — Trial Operations, Mexico City
hace 4 semanas
Mexico City ICON Strategic Solutions A tiempo completoA leading healthcare intelligence organization is seeking a Senior Clinical Supply Associate in Mexico City. The successful candidate will manage clinical trial supplies, ensuring compliance with regulations, and collaborate closely with clinical teams. Significant experience in clinical supply chain management and strong project management skills are...
-
Site Contract Lead
hace 3 semanas
Mexico City ICON Clinical Research A tiempo completoA leading clinical research organization in Mexico is seeking an Investigator Payment Lead responsible for negotiating and maintaining clinical trial agreements and amendments with study sites. The ideal candidate will demonstrate strong negotiation and communication skills, with a background in managing site contracts within clinical research. Additional...
-
Shanghai Clinical Trial Associate-Coordination
hace 3 semanas
Mexico City ICON A tiempo completoA global clinical research organization is seeking a Clinical Trial Administrator in Mexico City. In this role, you will assist with the coordination and administration of clinical trials, maintain documentation, and contribute to study preparation. Ideal candidates have a Bachelor's degree in a relevant field and strong communication skills, with an...
-
Clinical Supplies, Associate Manager
hace 2 días
Mexico City ICON Clinical Research A tiempo completoHome Based - MexicoICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.We are currently seeking a Clinical Supplies, Associate Manager to join our...