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- Tasks: Lead projects ensuring timely delivery of clinical supplies and approvals.
- Company: Join a dynamic pharmaceutical company focused on innovative clinical trials.
- Benefits: Enjoy a hybrid work model and gain valuable industry experience.
- Why this job: Make an impact in healthcare while developing your project management skills.
- Qualifications: Degree or equivalent experience required; project management experience essential.
- Other info: Contract role for 12 months with potential for extension.
The predicted salary is between 36000 - 60000 £ per year.
Job Description
Contract Role – Pharmaceutical Project Manager (Clinical Trials/ Clinical Supply Chain) — Liverpool/Hybrid – 12 Months Initial
We are seeking an experienced Pharmaceutical Project Manager (Clinical Trials/ Clinical Supply Chain) to support the External Manufacturing Quality team, due to the insourcing of newly acquired acquisition clinical trials.
Role Overview:• Job Title: Pharmaceutical Project Manager (Clinical Trials/ Clinical Supply Chain)• Location: Liverpool/Hybrid• Contract Type: Contract • Duration: 12 months initially• Sector: Pharmaceutical
Serves as Project Manager for prioritizing and alignment of external Qualified Person (QP) release of clinical supplies at Contract Manufacturing Organisations (CMOs).Partner with Regulatory Affairs and Global Clinical Supply Chain to ensure on-time delivery of Health Authority approvals for release of clinical supplies (as applicable).
Qualifications & Experience• Degree qualified or equivalent experience required.• Project Management experience is essential.• Previous Pharmaceutical Quality experience is desired/preferred.• Demonstrated experience leading initiatives related to continuous improvement and/or implementation of new ways of working.• Demonstrated ability to build and leverage relationships through diplomacy with a broader focus?within the Function.• Experienced in process improvement.• Ability to recognize the potential impact on internal/external challenges on the future state success.• Good knowledge/experience in computer systems (MS, excel, word, etc.).• Ability to co-ordinate/lead meetings.• Knowledge of clinical trial documentation submission and approval preferred.
Please feel free to contact myself – Daisy Nguyen at Gibbs Consulting for a confidential chat to know more details about the role.
Please also note: Due to the volume of applications received for positions, it will not be possible to respond to all applications and only applicants who are considered suitable for interview will be contacted.
Pharmaceutical Project Manager (Clinical Trials/ Clinical Supply Chain) employer: Gibbs Hybrid
Contact Detail:
Gibbs Hybrid Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Pharmaceutical Project Manager (Clinical Trials/ Clinical Supply Chain)
✨Tip Number 1
Make sure to highlight your project management experience in your conversations. Discuss specific projects you've managed, especially those related to clinical trials or supply chain, to demonstrate your expertise.
✨Tip Number 2
Network with professionals in the pharmaceutical industry, particularly those involved in clinical trials and quality assurance. Building relationships can provide insights and potentially lead to referrals for the position.
✨Tip Number 3
Familiarize yourself with the latest trends and regulations in clinical supply chains. Being knowledgeable about current practices will help you stand out during discussions and interviews.
✨Tip Number 4
Prepare to discuss your experience with process improvement initiatives. Be ready to share examples of how you've successfully implemented new ways of working in previous roles.
We think you need these skills to ace Pharmaceutical Project Manager (Clinical Trials/ Clinical Supply Chain)
Some tips for your application 🫡
Highlight Relevant Experience: Make sure to emphasize your project management experience, especially in the pharmaceutical sector. Detail any previous roles where you managed clinical trials or worked with external manufacturing quality teams.
Showcase Continuous Improvement Initiatives: Include specific examples of initiatives you've led that relate to continuous improvement or new ways of working. This will demonstrate your ability to drive change and enhance processes.
Demonstrate Relationship-Building Skills: Provide examples of how you've successfully built and leveraged relationships within a team or across departments. Highlight your diplomatic skills and ability to collaborate effectively.
Tailor Your Application: Customize your CV and cover letter to align with the job description. Use keywords from the job listing, such as 'clinical supply chain' and 'regulatory affairs', to ensure your application stands out.
How to prepare for a job interview at Gibbs Hybrid
✨Showcase Your Project Management Skills
Be prepared to discuss your previous project management experiences in detail. Highlight specific projects where you successfully led initiatives, particularly in the pharmaceutical sector, and how you managed timelines and resources.
✨Demonstrate Knowledge of Clinical Trials
Familiarize yourself with the clinical trial process and relevant documentation. Be ready to explain how your experience aligns with the requirements of managing clinical supplies and working with Contract Manufacturing Organisations (CMOs).
✨Emphasize Continuous Improvement Initiatives
Prepare examples of how you've implemented process improvements in past roles. Discuss any methodologies you used and the impact these changes had on efficiency or quality within your team or organization.
✨Build Rapport and Show Diplomacy
Since the role requires collaboration with various stakeholders, practice how you can build relationships through effective communication. Be ready to share examples of how you've navigated challenges and maintained positive working relationships in previous positions.
