Associate Clinical Project Manager, Sponsor Dedicated

IQVIA; Philadelphia (Philadelphia County); Remote; USD 82,000 - 187,000; Full time

Job summary

An established industry player seeks an Associate Clinical Project Manager to enhance clinical trial delivery. In this dynamic role, you will collaborate with clinical teams to ensure efficient project management, focusing on optimizing speed, quality, and compliance. You will be responsible for managing clinical studies, engaging with stakeholders, and driving operational excellence. This position offers an exciting opportunity to impact patient outcomes through innovative medical treatments. Join a forward-thinking company that values diverse talent and fosters a culture of collaboration and innovation, making a difference in the lives of patients worldwide.

Qualifications

• 2 years of clinical trial management experience required.
• Strong written and verbal communication skills in English.

Responsibilities

• Manage clinical studies ensuring speed, quality, and cost efficiency.
• Collaborate with functional groups to support milestone achievement.

Skills

Clinical Trial Management

Communication Skills

Problem Solving

Organization

Attention to Detail

Collaboration

Planning

Time Management

Prioritization

Education

Bachelor's Degree in Life Sciences

Tools

MS Office

Job description

*Home-based position

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 drugs 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

1. Provide input into the development of integrated study management plans with the core project team and/or sub-team.
2. 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.
3. Set objectives of project sub-team(s), according to agreed upon contract, strategy and approach, effectively communicate and assess performance.
4. Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles.
5. 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.
6. Identify risk (positive and negative) and contingencies and partner with project leader in problem solving and resolution efforts.
7. 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.
8. May serve as primary (for small projects) or back-up project contact with customer.
9. Lead the efforts of a project sub-team, responsible for managing cross-collaboration of the sub-team to support milestone achievement and to manage issues and obstacles.
10. Support the project leader in ensuring the financial success of the project.
11. Forecast and identify opportunities to accelerate activities to bring revenue forward in partnership with the senior project leader.
12. Identify changes in scope and partner with project leader to manage change control process as necessary.
13. Identify lessons learned and implement best practices.
14. May be assigned as the primary contact for vendors leading project vendor management and vendor management related activities as per project requirements.

Qualifications

1. Bachelor's Degree in life sciences or related field required
2. 2 years clinical trial management experience
3. Requires intermediate level knowledge of principles, theories, and concepts of a job area, typically obtained through advanced education combined with experience
4. 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.
5. Communication - Strong written and verbal communication skills including good command of English language. Strong presentation skills.
6. Problem solving - Strong problem solving skills.
7. 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.
8. Prioritization - Ability to handle conflicting priorities.
9. Quality - Attention to detail and accuracy in work. Results-oriented approach to work towards delivery and output.
10. IT Skills - Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel and PowerPoint.
11. Collaboration - Ability to establish and maintain effective working relationships with coworkers, managers and clients. Strong customer service skills.
12. Cross-collaboration - Ability to work across geographies displaying high awareness and understanding of cultural differences.
13. 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 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

The potential base pay range for this role, when annualized, is $82,400.00 - $186,600.00. 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.

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. Thank you for your interest in growing your career with us.

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