Assoc CPM

Within our sponsor dedicated team, we are looking for an Associate Clinical Project Manager who Leads and oversees the execution of clinical projects and research studies in accordance with global and local regulations to best meet customer needs while working toward organizational goals and strategies.

He/She will manages the delivery of clinical research studies from initiation to closeout; ensures that quality deliverables are presented on time and within budget; coordinates workstreams and cross-functional project teams while monitoring the use of consistent tools and methodologies; identifies and evaluates potential project risks and develops mitigation plans; and serves as the primary point of contact with the project sponsor.

Responsibilities

• Provide input in to the development of integrated study management plans with the core project team and/or sub-team

• Accountable for assigned portion 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 project 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 internal stakeholders. Support the project leader to prepare/present project and/or sub-team information proactively to external stakeholders.

• Identify risk (positive and negative) and contingencies and partner with project leader in problem solving and resolution efforts.

• Achieve project quality by identifying quality risks and issues, responding to issues raised by project sub-team members and partner with project leader planning/implementing appropriate corrective and preventative action plans.

• May serve as primary (for small projects) or back-up project contact with customer

Experience

• University background in Lifescience field

• Good knowledge of clinical world

• Previous 2/3 years' experience in Study Management Activities is highly recommended

• Fluency in English is a must!

• Location: Home-based

• Good interpersonal skills demonstrated as proactive, enthusiastic, and independent thinker

Your rewards:

• Career & development opportunities in a fast-paced environment - we are the leading CRO, opportunities are here!

• Exposure to top-tier research Institutions in the Country and to a Global network of colleagues working in high focus indications across Key therapy areas

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.