IQVIA Hiring For Manager
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IQVIA Hiring For Manager Role – Life Sciences Apply Online

IQVIA Hiring For Manager Role – Life Sciences Apply Online. Interested and eligible applicants can check out all of the details on the same below

If are you looking for some interview questions for the Assoc Clin Project Manager at IQVIA, then check the bottom of the page.

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Assoc Clin Project Manager

Primary Location: Bangalore, India

Additional Locations: Thane, India,IND

Type: Full time

Job ID: R1368679

JOB DESCRIPTION

Job Overview

Associate Project 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 Associate Project Lead 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 Associate Project Lead support the efforts of CPM to drive operational excellence and strategic leadership with our customers. Associate Project Leads may run their own studies, as part of their development.

Essential Functions

  • 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.
  • 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.
  • 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

  • Bachelor’s Degree Bachelor’s Degree in life sciences or other related field required Req
  • Typically requires 3 years of prior relevant experience.
  • Requires knowledge of principles, theories, and concepts of a job area, typically obtained through advanced education.
  • 3 years of relevant clinical research experience with analytical/financial skills or equivalent combination of education, training, and experience.
  • Knowledge of clinical trials – strong knowledge of clinical trial conduct and skill in applying applicable clinical research regulatory requirements i.e. International Conference on Harmonization (ICH), Good Clinical Practice (GCP), and relevant local laws, regulations, guidelines towards clinical trial conduct.
  • Communication – strong written and verbal communication skills including good command of the English language.
  • Focused – results-oriented approach to work delivery and output.
  • Problem-solving – problem-solving skills.
  • Organisation – planning, time management, and prioritization skills.
  • Prioritisation – the ability to handle conflicting priorities.
  • Quality – attention to detail and accuracy in work.
  • IT skills – good software and computer skills, including Microsoft Office applications, including but not limited to, Microsoft Word, Excel, and PowerPoint.
  • Collaboration – the ability to establish and maintain effective working relationships with coworkers, managers, and clients.
  • Cross-collaboration – the ability to work across geographies displaying high awareness and understanding of cultural differences.
  • Effective communication – the ability to lead and influence without authority.
  • IQVIA Core Competencies – the ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, innovation, Ownership). Lead by example.

APPLY ONLINE

If are you looking for some interview questions for the Assoc Clin Project Manager at IQVIA, then check the bottom of the page.

  1. Can you describe your experience in managing clinical studies and ensuring compliance with regulatory requirements such as ICH and GCP?
    • Answer: Yes, I have been actively involved in managing clinical studies for the past three years. I have a strong understanding of regulatory requirements and have implemented processes to ensure compliance with ICH and GCP guidelines. For example, I have developed and executed study management plans that adhere to these regulations while optimizing speed, quality, and cost of delivery.
  2. How do you approach risk management in clinical trial projects? Can you provide an example of a situation where you identified and mitigated a significant risk?
    • Answer: Risk management is crucial in clinical trial projects. I proactively identify risks, both positive and negative, and partner with the project leader to develop strategies for mitigating them. In a recent study, we faced a potential delay due to slow patient recruitment. I implemented targeted recruitment strategies, collaborated with site investigators, and successfully accelerated patient enrollment, mitigating the risk of timeline delays.
  3. Describe your experience in managing project teams and ensuring effective collaboration across functional groups.
    • Answer: I have experience in leading project sub-teams and fostering cross-functional collaboration. In my previous role, I led a project sub-team responsible for milestone achievement and issue resolution. I effectively communicated objectives, assessed performance, and facilitated collaboration among team members from different functional groups to ensure timely project delivery. Through regular meetings and open communication channels, we achieved successful outcomes.
  4. How do you handle changes in project scope and manage the change control process?
    • Answer: Changes in project scope are common in clinical trials. I approach them by closely monitoring project progress and assessing the impact of scope changes on timeline, resources, and budget. When necessary, I collaborate with the project leader to initiate the change control process, which involves evaluating the proposed changes, documenting them, and obtaining necessary approvals. By following this structured approach, I ensure effective management of scope changes without compromising project objectives.
  5. Can you provide an example of how you have contributed to the financial success of a clinical trial project?
    • Answer: In a recent project, I actively contributed to the financial success by identifying opportunities to accelerate activities and bring revenue forward. Through careful forecasting and strategic planning, I identified areas where we could expedite certain study activities without compromising quality or compliance. By executing these plans, we successfully accelerated timelines, optimized resource utilization, and achieved financial goals while maintaining high-quality standards.

Note: The answers provided here are for reference and can be tailored based on the individual’s actual experience and achievements.

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