Manager, Vendor & Third-Party Management - FSP
Manager, Vendor & Third-Party Management - FSP
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
Job Description
When our values align theres no limit to what we can achieve.
At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us no matter what we do at Parexel contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally we do it with empathy and were committed to making a difference.
Parexel is currently seeking a and experienced Clinical Vendor Manager to join us. You will be assigned to one of our key sponsors in the region.
Working as a Clinical Vendor Manager at Parexel FSP offers tremendous long-term job security and prospects. We undertake vital clinical studies for sponsors including the leading global biotechs and Pharma top 50. And we have an incredible pipeline of work.
Whether you see your future path in fields such as clinical operations project management line management or other positions we have a world of opportunity waiting for you.
Our staff work from their home office base supporting studies within their country or region. Expect exciting professional challenges in inspiring studies but with time for your outside life.
Some specifics about this advertised role
- Dedicated to one client.
- Act as the V&TPM Single Point of Contact (SPOC) for the Evidence Generation team providing guidance and support throughout third-party interactions.
- Coordinate V&TPM activities and responsibilities with Evidence Generation study teams (Study Execution Evidence Generation).
- Oversee the end-to-end process including liaison with Legal qualification RFP contracting and PO management.
- Interface with stakeholders and Novartis functions providing inputs and updates as needed.
- Manage qualification project timelines and proactively alert stakeholders to deviations or risks.
- Ensure all third-party activities are conducted in alignment with internal policies and external regulatory requirements.
- Monitor and support risk identification assessment and mitigation strategies related to third-party engagements.
Here are a few requirements specific to this advertised role.
- Degree in a life science or health care discipline
- Previous experience in clinical vendor management or similar role with focus on clinical research is a plus but not required.
- Clinical Trial/Medical Affairs experience in a pharmaceutical company or a contract research organization is required.
- Project management experience in clinical operations in a pharmaceutical company or a contract research organization. Emphasis on business experience with clinical/medical affairs processes and activities and associated external services with excellent understanding of study management.
- Good knowledge of the regulatory requirements in Clinical Research and drug development:
- In-depth knowledge of the international pharmaceutical product development process
- Experience with GxP requirements quality management system including risk management and regulatory requirements from main Health Authorities.
- A broad understanding of main Health Authorities standards (e.g. FDA EMEA) and ICH regulations and guidelines.
- A broad understanding of Quality Management GCP / GVP and Risk Management processes
We care about our people and your passion as they are the key to our success and provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long-term careers. In addition you will have the opportunity to develop within your role and tackle further responsibilities or develop your skill set within other related departments of Parexel.
Who are Parexel
Parexel supports clinical studies across the full range of therapeutic areas and we have longstanding partnerships with a vast client base.
We supported the trials of most of todays top 50 best-selling drugs but equally we enable more niche drug developments that are critical to the well-being of many patients.
Youll be an influential member of the wider team.
Not quite the role for you
Join Our Talent Community and well reach out with job alerts when positions that match your career interests become available. Well also share periodic updates about the latest company news and events.
Sign up today Experience:
Manager
Employment Type
Full-Time
Key Skills
Similar Jobs
Dr. Job is an online platform that connects employers with skilled job seekers, facilitating the search for job opportunities and top talent. Established in 2015. Dr. Job Pro has emerged as the world premier job portal, attracting thousands of job seekers every day from all over the world.
Follow Dr.Job
Dr Job FZ LLC. 2025 © All Rights Reserved