Job description
Qarad’s IVD CROis a clinical research organization (CRO) specializing in In Vitro Diagnostics (IVD), providing full-service solutions to support diagnostic development from concept to commercialization. With a growing portfolio of projects, we are dedicated to delivering high-quality outcomes through excellence in project execution and governance.
We are seeking a dynamic and experienced Project Managerto join our team, specializing inclinical performance studies for In Vitro Diagnostic devices (IVD).
You will play a critical, dual role within our organization. On the one hand, you manage individual high-value, strategic projects that align with our business goals. On the other hand, you will take responsibility for overall project planning and ensuring the successful execution of all projects within the IVD CRO organization. This includes driving adherence to project governance procedures, supporting study coordinators, and implementing tools and processes to enhance project management capabilities in an efficient and dynamic way.
The role requires an experienced, hands-on leader with strong organizational skills, and proven experience in managing complex projects. If you're ready to make a significant impact in a role that combines organizational skills, and customer engagement, we invite you to join our team and help us drive the future of clinical performance studies.
What do we expect from you as a sr Project Manager IVD CRO?
Project Governance and oversight :
Oversee the planning and execution of all projects within the team, ensuring adherence to project governance processes and ensuring efficient follow up of interdependent projects.
Support and guide Study Coordinators, enabling them to achieve success and deliver consistent results.
Implement project management tools, and templates across the team to increase operational efficiency.
Continuously monitor project portfolios for risks, deviations, and resource utilization, driving actions for improvement as needed.
Project Management :
Lead the planning, execution, and deliveryof critical strategic projects, ensuring timely and high-quality outcomes within budget.
Serve as theprimary point of contact for clients and stakeholders, fostering strong relationships, transparency, and effective communication.
Identify risks, create mitigation plans, and ensure proactive issue resolution to keep projects on track.
Develops and manages the study budget. Overall responsibility for negotiation of financial aspects of clinical performance studies / program.
Interacts with senior internal management and external personnel on significant matters often requiring coordination between involved team members and stakeholders.
Uses discretion, diplomacy and tact to resolve difficult situations. Escalates serious issues to management.
Who are we looking for?
Master’s, or Ph.D. in a relevant scientific discipline (e.g., Biomedical Sciences, Biotechnology, Bioscience Engineering, ...) or equivalent by experience
Minimum of 7 years’ experience in project management, with a proven track record in a CRO, IVD, medical device, or life sciences environment.
Experience with managing complex, cross-functional projects with global stakeholders.
Exceptional leadership, communication, and stakeholder management skills.
Pragmatic and hands-on.
Proven ability to develop and implement project management tools, systems, and best practices.
Stronganalytical and problem-solving skillswith a strategic mindset.
High attention to detail and organizational skills.
Ability to identify and adapt to shifting priorities and competing demands
Excellent interpersonal skills; Team player
Ability to make timely and well-reasoned decisions
Abilityto effectively and persuasively communicate verbally and in writing
Sensitive to cultural differences
Fluent in English. Other languages are a plus
Strong experience using Microsoft applications (Excel, Word, PowerPoint, Outlook)
A true QbD’er can be recognized by the following qualities:
Resilient: Your strong and positive attitude helps you overcome any challenge
Hungry for knowledge: You are always open to learning
No non-sense mentality: you can be straightforward in a respectful way
Innovative: You are constantly looking for new and better solutions
(Not too) serious: your job is serious, but you don’t take yourself too serious.
What’s in it for you?
QbD Group offers you an attractive and competitive salary package, that will be tailored to individual needs, considering legal requirements and local laws and regulations.
Join us to build a sustainable career, where job security is ensured, and lasting, meaningful connections are formed.
As we’re a knowledge-based company, you’re guaranteed to embark on a continuous journey of learning and development.
Be part of our global success story. As an award-winning company we value everyone’s contribution and celebrate achievements together
Our promise to you:
As an ambitious and pioneering company, we want to offer you the best possible environment to thrive within the life sciences.
Moreover, we aim to create a joyful communitywhere you dare to be and can be yourself. Because the best way to grow is by growing together as unique individuals.
In short … We stand for? JPEG: Joy in Partnership, going for the Extra mile to Get things done!
Interested?Send us your CV and motivation letter and who knows, we might welcome you soon in our QbD family!
Originally posted on Himalayas
Who can apply
Eligible countries: United States. Accepted UTC offsets: UTC-10, UTC-9, UTC-8, UTC-7, UTC-6, UTC-5, UTC+14. Review the full description for employer-specific work authorization, residency and schedule requirements.