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Associate Project Manager

Overview

We currently have an exciting new opportunity for an Associate Project Manager to join our growing team, sponsor dedicated.

The Associate Project Manager is a member of the extended global study team supporting delivery of clinical studies within BioPharmaceuticals Clincal Operations, Study Management.

 

This is a permanent role with ICON on FSP and fully home-based.  You must be located in the following countries to be consider:  Bulgaria, Poland OR Spain. 

 

Start date: June, July and August 1st 2025

Responsibilities

  • Leads/contributes to the preparation of delegated study documents (e.g., Informed Consent Form, master Clinical Study Agreement etc), and external service provider related documents (specifications, study specific procedures, descriptions, presentations etc.).
  • Maintains and facilitates interactions with internal functions and external functions including the CROs and other external service providers to ensure an efficient study delivery to time, costs and quality objectives.
  • Contributes to the planning and conduct of internal and external meetings (e.g., Investigators’/Monitors’ meeting).
  • Ensures the supply of Investigational product and study materials by liaising with Clinical Supply Chain or external service providers as appropriate.
  • Proactively contributes to risk and issue identification, development of mitigation and/or action plans for identified risks and issues.
  • Ensures that all study documents in scope of global associate project manager responsibilities are complete and verified for quality in Trial Master File.
  • Supports Global Study Directors and/or GSAD with budget management, such as external service provider invoice reconciliation.
  • Adheres to global clinical processes, procedural documents, applicable Quality & Compliance manual documents and international guidelines such as ICH/GCP to ensure study is inspection ready at all times.
  • Supports Global Study Directors and/or GSAD with overall project management as per agreed delegation.
  • For outsourced studies, supports Global Study Directors and/or GSAD in management of the CRO Project Manager to ensure study delivery according to agreed timelines, budget and quality standards, while ensuring that the appropriate level of oversight of the CRO is maintained and documented throughout the lifecycle of the study

Qualifications

  • University degree (or equivalent), preferably in medical or biological sciences or discipline associated with clinical research.Relevant experience from within the pharmaceutical industry or similar organization or academic experience, preferably of at least 3 years.
  • Vendor management experience
  • Knowledge of clinical development /drug development process in various phases of development and therapy areasExcellent knowledge of international guidelines ICH/GCP
  • Excellent communication and relationship building skills, including external service provider management skills
  • Good project management skills
  • Demonstrated ability to collaborate as well as work independently
  • Demonstrated leadership skills
  • Computer proficiency, advanced

 

  • You MUST be located in the following countries to be considered: Poland, Spain OR Bulgaria, no other countries will be considered at this time.
  • You MUST come from a Clinical Research background

CRA backgrounds are not considered. 

 

Job profiles that would be considered:

  • Global Senior Project Specialist with Project Management tasks
  • Vendor Manager within a pharma/CRO setting driving the global delivery of study management activities
  • Associate Project Manager within CRO or Pharma setting driving global delivery of study management activities. 

 

What You Should Know About Associate Project Manager, Pharmaceutical Research Associates, Inc

Are you ready to take your career to the next level as an Associate Project Manager with ICON? This is an amazing opportunity to join a vibrant and dedicated team in the BioPharmaceuticals Clinical Operations space. In this fully home-based role, you’ll be an integral part of the global study team, supporting the delivery of crucial clinical studies. If you’re in Bulgaria, Poland, or Spain, we want to hear from you! As an Associate Project Manager, your responsibilities will include preparing key study documents, maintaining smooth interactions with internal and external partners, and contributing to the planning of vital meetings. You’ll also ensure timely supply of Investigational products while effectively managing risks. Your expertise will help maintain high-quality standards in the Trial Master File and support budget management for our Global Study Directors. With at least three years of experience in the pharmaceutical industry or academic environment, coupled with your project management skills, you will thrive in this collaborative and fast-paced setting. If you're passionate about clinical research and looking to grow your career in a supportive environment, this role with ICON could be the perfect fit for you. Join us and help shape the future of clinical studies, where your efforts will help drive efficiency and excellence every step of the way!

Frequently Asked Questions (FAQs) for Associate Project Manager Role at Pharmaceutical Research Associates, Inc
What are the main responsibilities of an Associate Project Manager at ICON?

As an Associate Project Manager at ICON, you will be responsible for preparing delegated study documents, maintaining effective communication with internal and external partners, and contributing to meeting planning. Additionally, you will manage the supply of investigational products, support global study directors with budget management, and ensure that all study documents are complete and verified for quality in the Trial Master File.

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What qualifications do I need to be an Associate Project Manager at ICON?

To qualify as an Associate Project Manager at ICON, you should have a university degree in a relevant field such as medical or biological sciences. You also need at least three years of relevant experience in the pharmaceutical industry, particularly in project management or clinical research. Strong communication skills and knowledge of clinical development processes are essential.

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What kind of work environment can I expect as an Associate Project Manager at ICON?

As an Associate Project Manager at ICON, you'll enjoy a fully home-based work environment that promotes flexibility and work-life balance. You'll be part of a collaborative global study team that fosters innovation and efficiency in clinical studies, allowing you to thrive in a supportive and engaged culture.

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Is previous experience in clinical research required for the Associate Project Manager position at ICON?

Yes, having a background in clinical research is a must for the Associate Project Manager role at ICON. Candidates with experience in related disciplines, such as vendor management or global project management within a CRO or pharmaceutical setting, will have a competitive edge.

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What locations are eligible for the Associate Project Manager role at ICON?

The Associate Project Manager position at ICON is available for candidates located in Bulgaria, Poland, or Spain. Unfortunately, candidates from other countries will not be considered for this fully remote position.

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Common Interview Questions for Associate Project Manager
Can you describe your experience with clinical study documentation?

When answering this question, be sure to outline any previous roles where you prepared clinical study documents, such as Informed Consent Forms or Clinical Study Agreements. Emphasize your attention to detail and understanding of regulatory requirements while showcasing relevant examples.

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How do you manage communication with external vendors?

Highlight your experience in building relations with external vendors and how you maintain clear communication throughout a project’s lifecycle. Discuss strategies you’ve implemented that fostered collaboration and resolved conflicts, ensuring project timelines were met.

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Describe a time when you identified a risk in a project. What did you do?

Use the STAR method (Situation, Task, Action, Result) to guide your response. Discuss how you proactively identified the risk, the mitigation plan you executed, and the outcome. This illustrates your problem-solving skills and proactive approach.

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What project management tools are you familiar with?

Mention specific project management tools you've used, such as MS Project, Asana, or Trello. Explain how you utilized these tools in managing timelines, resources, and team communications during your previous projects.

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How do you handle tight deadlines?

Share your strategies for prioritizing tasks and managing time effectively under pressure. Use examples from previous experiences where you successfully met tight deadlines without compromising quality.

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What do you understand about ICH/GCP guidelines?

Provide a brief overview of your knowledge regarding ICH and GCP guidelines, emphasizing their importance in clinical trials. You might discuss how your adherence to these regulations has contributed to successful project outcomes in the past.

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How would you ensure quality in the Trial Master File?

Detail your approach to maintaining quality documentation, including regular audits and check-ins with team members. Emphasize your understanding of regulatory requirements and your commitment to keeping the Trial Master File inspection-ready at all times.

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Can you give an example of a successful meeting you facilitated?

Present a scenario where you planned and facilitated a meeting that led to key decisions or outcomes in a project. Highlight your preparation, the structure of the meeting, and the impact it had on the project’s success.

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What strategies do you employ for effective budget management?

Discuss your experience working with budgets and invoices, outlining methods you use to track expenses and ensure financial resources are allocated efficiently. You can provide an example where your financial oversight positively influenced project delivery.

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Why do you want to work as an Associate Project Manager at ICON?

Express your interest in the role by mentioning the company's reputation in clinical research and your passion for contributing to the field. Highlight how the position aligns with your career goals and how you can add value to the team.

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DATE POSTED
March 28, 2025

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