FSP Clinical Project Manager

IQVIA LLC; Durham, Northern (NC, KY); Hybrid; USD 93,000 - 233,000; Full time

Job summary

IQVIA LLC seeks an experienced FSP Clinical Project Manager in Durham, NC to drive delivery of clinical studies in line with contracts and SOPs. You will develop and own integrated study management plans, lead core project teams, and ensure on-time, on-budget execution with quality.

The role requires a Life Sciences degree and 5+ years of experience including project management, with strong English communication and regulatory knowledge (ICH GCP).

Qualifications

• Bachelor's degree in Life sciences or related field (Req).
• 5+ years of relevant experience including >1 year project management experience or equivalent.
• Knowledge of clinical trials and regulatory requirements (ICH GCP) and applicable local laws.
• Strong communication skills in English; effective presentation abilities.
• Ability to lead cross-functional teams and manage project deliverables and timelines.
• Experience managing project finances and contract obligations.

Responsibilities

• Lead delivery of clinical studies in accordance with contracts, SOPs and practices.
• Develop integrated study management plans with the core project team.
• Own project execution to optimize speed, quality and cost while ensuring training and tools compliance.
• Set objectives for teams and monitor performance with stakeholders.
• Collaborate with functional groups to meet milestones and resolve issues.
• Proactively report project status, risks and change controls to stakeholders.

Skills

Project management

Clinical trials knowledge

Communication skills

Leadership

Problem solving

Organization

Budgeting / finances

Regulatory compliance (ICH GCP)

Cross-functional collaboration

MS Office (Word/Excel/PowerPoint)

Education

Bachelor's degree in life sciences or related field

Tools

MS Office

Excel

PowerPoint

Job description

FSP Clinical Project Manager page is loaded## FSP Clinical Project Managerlocations: Durham, North Carolina, United States of Americatime type: Full timeposted on: Posted Todayjob requisition id: R1569250Job OverviewProject Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients' lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and practices. Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. Clinical Project leads can run their own studies. The Project Lead focus is on leveraging therapeutic expertise and IQVIA's suite of solutions to drive operational excellence and strategic leadership with our customersEssential Functions- Participate in bid defense presentations in partnership with Business Development and may lead the presentation for smaller, less complex regional studies.- May be responsible for delivery and management of smaller, less complex, regional studies.- Develop integrated study management plans with the core project team.- Accountable for the execution of clinical studies, or assigned portion of clinical studies, per 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 and/or sub-team(s) 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 and/or sub-team information proactively to stakeholders internally and externally.- 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 and/or sub-team members and planning/implementing appropriate corrective and preventative action plans.- May serve as primary or backup project contact with customer and would then own the relationship with the project's key customer contacts, as well as 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 lessons learned and implement best practices.- May be assigned as the primary contact for vendors leading project vendor management and vendor management related activities as per project requirements.;- 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 and mentor less experienced project team members on assigned projects to support their professional development.;Qualifications- Bachelor's Degree Life sciences or related field Req- 5 years of prior relevant experience including > 1 years project management experience or equivalent combination of education, training and experience. Req- Advanced knowledge of job area, and broad knowledge of other related job areas, typically obtained through advanced education combined with experience. Req- 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. Broad protocol knowledge; therapeutic knowledge desired. Good understanding of the competitive environment and how to communicate/demonstrate value through IQVIA solutions.;- Communication - Strong written and verbal communication skills including good command of English language. Strong presentation skills.- Problem solving - Strong problem solving skills.- Leadership - Ability to work through others to deliver results to the appropriate quality and timeline metrics, monitoring/managing performance and providing feedback, experience productively partnering cross functionally and with customers to advance work effectively and efficiently.- Leadership - Ability to make decisions, bringing clarity to disparate information to inform actions and drive results.- Organization - Planning, time management and prioritization skills. Ability to organize resources needed to accomplish tasks, set objectives and provide clear direction to others, experience planning activities in advance and taking account of possible changing circumstances.- Prioritization - Ability to handle conflicting priorities.- Quality - Attention to detail and accuracy in work. Results-oriented approach to work towards delivery and output.- Quality - Demonstrated learning agility and openness to learning and keeping own knowledge and skill set current and evolving.- IT skills - Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel and PowerPoint.- Collaboration - Ability to establish and maintain effective working relationships with coworkers, managers and clients. Strong customer service skills.- Cross-collaboration - Ability to work across geographies displaying high awareness and understanding of cultural differences.- Finances - Good understanding of project financials including experience managing, contractual obligations and implications.- IQVIA Core Competencies - Ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, innovation, Ownership).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 atIQVIA 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.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