Clinical Project Manager, IQVIA Biotech

IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. The company has an agile structure, collaborative culture, and deep therapeutic expertise to deliver tailored solutions that help bring innovative treatments to patients faster.

• Bachelor's Degree in Life Sciences or related field.
• Minimum 5 years of relevant experience including over 1 year of project management experience or equivalent combination of education, training, and experience.
• Advanced knowledge of job area, typically obtained through advanced education combined with experience.
• Knowledge of clinical trial conduct and skill in applying clinical research regulatory requirements such as ICH GCP and relevant local laws, regulations, and guidelines.
• Broad protocol knowledge; therapeutic area knowledge in cardiovascular, metabolic, renal, or obesity is an advantage.
• Good understanding of project financials including managing contractual obligations and implications.
• Good understanding of the competitive environment and ability to communicate value through IQVIA Biotech solutions.
• Strong written and verbal communication skills with very good command of English.
• Strong customer service skills and presentation abilities.
• Ability to work through others to deliver results with appropriate quality and timeline metrics; experience partnering cross-functionally and with customers.
• Ability to make decisions by clarifying disparate information to inform actions and drive results.
• Planning, time management, and prioritization skills.
• Ability to organize resources, set objectives, and provide clear direction; experience planning activities in advance considering changing circumstances.
• Results-oriented approach.
• Demonstrated learning agility and openness to continuous learning.
• Good software and computer skills.
• Ability to work across geographies with high awareness and understanding of cultural differences.
• May require occasional travel to the United States.

• Accountable for execution of clinical studies or assigned portions per contract, optimizing speed, quality, and cost while ensuring compliance with standard processes, policies, and procedures.
• Set objectives for the core project team according to contract, strategy, and approach; communicate and assess performance.
• Participate in bid defense presentations with Business Development; may lead presentations for smaller, less complex regional studies.
• Responsible for delivery and management of smaller, less complex, regional studies.
• Develop integrated study management plans with the core project team.
• Collaborate with other functional groups to support milestone achievement and manage study issues and obstacles.
• Monitor progress against contract and prepare project information proactively for internal and external stakeholders.
• Manage risks and contingencies proactively; lead problem solving and resolution efforts.
• Achieve project quality by identifying risks and issues, responding to team concerns, and implementing corrective and preventative actions.
• May serve as primary or backup project contact with customer, owning relationships with key customer contacts and collaborating with IQVIA business development representatives.
• Build and lead the cross-functional project team; manage cross-collaboration and overall project delivery to support milestones and manage study issues.
• Ensure financial success of the project.
• Forecast and identify opportunities to accelerate activities to bring revenue forward.
• Identify scope changes and manage change control process as necessary.
• Provide input to line managers on project team members' performance relative to project tasks.
• Support staff development and mentor less experienced project team members to support their professional development.

IQVIA maintains a zero tolerance policy for candidate fraud. All information and credentials submitted must be truthful and complete. False statements, misrepresentations, or material omissions during recruitment will result in disqualification or termination in accordance with applicable law.