Associate Clinical Project Manager Sponsor Dedicated
Associate Clinical Project Manager Sponsor Dedicated
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
$ 82400 - 186600
1 Vacancy
Job Description
Two years of clinical trial management experience is required
Job Overview
Associate Clinical Project Managers (aCPM)/Local Trial Managers are an integral part of clinical trial delivery liaising with clinical teams to improve patients lives by bringing new to the market faster. The aCPM is a 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. The aCPM supports the efforts of CPM to drive operational excellence and strategic leadership with our customers.
Essential Functions
Provide input in to the development of integrated study management plans with the core project team and/or subteam.
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 subteam(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 subteam information proactively to internal stakeholders. Support the project leader to prepare/present project and/or subteam 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 subteam members and partner with project leader planning/implementing appropriate corrective and preventative action plans.
May serve as primary (for small projects) or backup project contact with customer.
Lead the efforts of a project subteam responsible for managing crosscollaboration of the subteam to support milestone achievement and to manage issues and obstacles.
Support the project leader in ensuring the financial success of the project.
Forecast and identify opportunities to accelerate activities to bring revenue forward in partnership with the senior project leader.
Identify changes in scope and partner with project leader to 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.
Qualifications
Bachelors Degree In life sciences or related field required
2 years clinical trial management experience
Requires intermediate level knowledge of principles theories and concepts of a job area 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. Broad protocol knowledge therapeutic knowledge desired.;
Communication Strong written and verbal communication skills including good command of English language. Strong presentation skills.
Problem solving Strong problem solving skills.
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. Resultsoriented approach to work towards delivery and output.
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.
Crosscollaboration Ability to work across geographies displaying high awareness and understanding of cultural differences.
Finances Good understanding of project financials.
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 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. potential base pay range for this role when annualized is $82400.00 $186600.00. The actual base pay offered may vary based on a number of factors including jobrelated qualifications such as knowledge skills education and experience; location; and/or schedule (full or parttime). 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.
Required Experience:
IC
Employment Type
Full-Time
