Senior Clinical Project Manager

Essential Functions - Participate in bid defense preparations. Lead bid defense presentations in partnership with Business Development for, multiple service, multiple country and/or multi regional studies.

Understand project strategy and operationalize the agreed upon approach. - Develop integrated study management plans with the core project team. - Accountable for the strategic planning and execution of clinical studies as per the contract while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures. - Set objectives of the core project team according to agreed upon contract, strategy and approach, effectively communicate and assess performance. - Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles. - Monitor progress against contract and prepare/present project information proactively to all stakeholders internally and externally. - Responsible for delivery and management of medium to large sized, multiple and full service, multi regional studies. - Manage risk (positive and negative) and contingencies proactively and lead problem solving and resolution efforts. - Achieve project quality by identifying quality risks and issues, responding to issues raised by project team members and planning/implementing appropriate corrective and preventative action plans.; - Serve as primary project contact with customer and own relationship with the project's key customer contact(s) - Communicate/collaborate with IQVIA business development representatives as necessary. - Build the cross-functional project team and lead their efforts, responsible for managing cross-collaboration of the core team and for overall project delivery to support milestone achievement and to manage study issues and obstacles.; - Ensure the financial success of the project. - Forecast and identify opportunities to accelerate activities to bring revenue forward. - Identify changes in scope and manage change control process, as necessary. - Identify and communicate lessons learned and best practices to promote continuous improvement. - Adopt corporate initiatives and changes and serve as a change advocate when necessary. - Provide input to line managers of 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.

Qualifications - Bachelor's Degree Life sciences or related field Req - Minimum of 7 years of clinical research experience within a CRO or Pharmaceutical/Biotechnology environment, including at least 4 years of clinical trial management experience. - Experience in all aspects of clinical study planning and startup, including budget and resource planning, and execution of clinical study activities from startup through final study report. - Significant professional experience in relevant disciplines, with substantial project management experience and senior-level knowledge within the field. - Strong leadership competencies and influencing skills. - Effective verbal and written communication skills. - Demonstrated ability to foster partnerships across projects and multidisciplinary teams. - Good understanding of the drug development process, including the interfaces and interdependencies between clinical development and other functions such as nonclinical and pharmaceutical development, regulatory, and commercial/marketing.

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 https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe 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. The potential base pay range for this role, when annualized, is $93,100.00 - $232,800.00. 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.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.