At a Glance
- Tasks: Lead client software implementation projects in pharmacovigilance technology.
- Company: Join Qinecsa, a global leader in pharmacovigilance solutions for life sciences.
- Benefits: Enjoy competitive salary, remote work options, and professional development opportunities.
- Why this job: Be part of an innovative team making a real impact in healthcare safety.
- Qualifications: Bachelor's or Master's degree with 8+ years in project management, preferably in life sciences.
- Other info: Mentorship opportunities available; work with world-class clients.
The predicted salary is between 43200 - 72000 £ per year.
About the Company
Qinecsa is a trusted, global partner bringing together best-in-class technology and scientific expertise to connect life science companies, public health, and regulatory sectors to the right safety solutions. We take pride in being the leading specialist pharmacovigilance provider, offering unparalleled expertise in PV services, technology, and consulting to cater to the unique needs of small, medium, and large pharmaceutical companies.
We are seeking a Consulting Technology Project Manager to manage client implementation projects for our Pharmacovigilance SaaS solutions. The ideal candidate will be a dynamic client-facing services professional with extensive project management experience in the life science technology domain. This is a strategic role requiring deep project management expertise, pharmaceutical domain knowledge, and excellent leadership skills.
Key Responsibilities:
- Lead end-to-end project management of client software implementations, upgrades, and integrations.
- Develop and manage project plans, including timelines, budgets, and resource demand, and author project initiation documents.
- Coordinate cross-functional, global teams to ensure successful project delivery.
- Serve as the primary point of contact for senior client stakeholders, ensuring clear communication and strong relationship management.
- Ensure the accuracy, reliability, and performance of all project deliverables.
- Monitor project progress and performance, identifying and mitigating risks and issues as they arise.
- Facilitate regular project status meetings and provide updates to stakeholders.
- Actively manage project scope and costs, ensuring any changes are documented and approved through formal change control processes.
- Develop and maintain comprehensive project documentation, including project initiation documents, risk management plans, and post-project reviews.
- Ensure all projects comply with industry regulations, particularly those related to pharmacovigilance and data privacy (e.g. GxP, GDPR).
- Coordinate and manage interactions with third-party vendors, consultants, and partners to ensure successful delivery and integration of external components or services.
- Support continuous improvement of project management processes, tools, and best practices within the organization.
- Mentor and guide junior project managers and team members, fostering a collaborative and high-performance team environment.
Characteristics:
- Well-organized self-starter with attention to detail.
- Excellent client-facing communication and problem-solving skills.
- Strong written, communication, and interpersonal skills.
- A desire to learn about our proprietary products.
Essential Experience and Qualifications:
- Bachelor's or Master's degree in Computer Science, Information Technology, Project Management, or a related field.
- 8+ years of experience in project management, with at least 5 years in a senior or lead role delivering software solutions to pharmaceutical or life sciences clients.
- Proven experience managing pharmacovigilance, clinical, or regulatory technology projects.
- Knowledge of pharmacovigilance workflows and regulatory standards (e.g., ICH E2E, GVP Modules, FDA, EMA).
- Expertise in project management methodologies (e.g., Agile, Scrum, Waterfall).
- Proficiency in project management tools (e.g., Microsoft Project, Jira, SmartSheet).
Preferred Experience and Qualifications:
- Familiarity with signal detection, case management, and safety databases (e.g., Argus, ARISg).
- Familiarity with cloud-based solutions and big data technologies.
- Technical background with experience in software development or IT infrastructure.
- Knowledge of regulatory requirements and industry standards for technology solutions.
- Certification in project management (e.g., PMP, PRINCE2).
What We Offer:
- Competitive salary.
- Opportunity to work with a dynamic and innovative team and world-class clients.
- Professional development and growth opportunities.
- A collaborative and inclusive work environment.
- Work from home with limited travel.
How to Apply:
Interested candidates are invited to submit their resume and cover letter to roopa.shree@qinecsa.com.
Consulting Project Manager (PV Systems) (United Kingdom) employer: Qinecsa Solutions
Contact Detail:
Qinecsa Solutions Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Consulting Project Manager (PV Systems) (United Kingdom)
✨Tip Number 1
Familiarise yourself with pharmacovigilance workflows and regulatory standards. Understanding the specific requirements of the industry will not only help you in interviews but also demonstrate your commitment to the role.
✨Tip Number 2
Network with professionals in the life sciences and project management fields. Attend relevant conferences or webinars to connect with potential colleagues and learn more about the latest trends in pharmacovigilance technology.
✨Tip Number 3
Brush up on your project management methodologies, especially Agile and Scrum. Being able to discuss these frameworks confidently can set you apart from other candidates during interviews.
✨Tip Number 4
Prepare to showcase your leadership skills by thinking of examples where you've successfully managed teams or projects. Highlighting your ability to mentor others will resonate well with the hiring team at Qinecsa.
We think you need these skills to ace Consulting Project Manager (PV Systems) (United Kingdom)
Some tips for your application 🫡
Understand the Role: Before applying, make sure to thoroughly understand the responsibilities and qualifications required for the Consulting Project Manager position. Tailor your application to highlight relevant experience in project management within the life sciences sector.
Craft a Compelling Cover Letter: Your cover letter should not only express your interest in the role but also demonstrate your understanding of pharmacovigilance and project management methodologies. Use specific examples from your past experiences that align with the job description.
Highlight Relevant Experience: In your CV, focus on your project management experience, especially in the pharmaceutical or life sciences domain. Include details about the projects you've managed, the methodologies used, and any regulatory standards you are familiar with.
Proofread Your Application: Ensure that your CV and cover letter are free from grammatical errors and typos. A well-presented application reflects your attention to detail, which is crucial for the role of a Consulting Project Manager.
How to prepare for a job interview at Qinecsa Solutions
✨Understand the Company and Its Services
Before your interview, make sure you have a solid understanding of Qinecsa's role in pharmacovigilance and the specific SaaS solutions they offer. This knowledge will help you demonstrate your interest and show how your experience aligns with their needs.
✨Highlight Relevant Project Management Experience
Be prepared to discuss your past project management experiences, especially those related to pharmacovigilance or life sciences. Use specific examples to illustrate your ability to lead projects, manage budgets, and coordinate teams effectively.
✨Showcase Your Communication Skills
As this role involves significant client interaction, emphasise your communication skills. Prepare to discuss how you've successfully managed client relationships and facilitated project updates in previous roles.
✨Familiarise Yourself with Regulatory Standards
Since the position requires knowledge of regulatory standards like GxP and GDPR, brush up on these topics. Being able to speak confidently about compliance issues will set you apart as a candidate who understands the industry's complexities.