LOCAL START UP PROJECT MANAGER, PARIS, CLIENT DEDICATED

Job Overview:

Ready to expand your Start up / Regulatory career towards Project Management?

In France, our sponsor dedicated team continues its expansion, and we have a new opportunity for a Local Start-up Project Manager

THE LOCAL START UP PROJECT MANAGER / PM JOB

  You will work sponsor dedicated for a prestigious Top 5 global Pharmaceutical company. This job is located in Paris , and we are prepared to offer a combination of home & office based work.

The job is perfect to gain a combined and rich experience within the CRO and Sponsor environments. It would suit existing:

  CRO-based Senior Start-up Specialists or Local Start Up Project Managers looking for a closer partnership with a Sponsor, or Biopharmaceutical based Start-up Managers looking to have experience within a Global CRO.

You will have significant impact on how France deliver local Start-up, Regulatory and financial compliance commitments and objectives. As the main Local Operational responsible person in the country, your responsibilities will include, among others:

FINANCIAL

  Assistance with the ownership of country and site budgets. Through continual interaction with local clinical team/s successfully delivers clinical and financial contracts. Oversight and tracking of clinical research-related payments Payment reconciliation at study close-out.

COUNTRY SUBMISSIONS & LOCAL LANGUAGE MATERIALS Responsible for execution and oversight of clinical trial country submissions and approvals for assigned protocols. Development of local language materials including local language Informed Consents and translations.

MANAGEMENT & QUALITY OVERSIGHT: Responsible for managing country deliverables, timelines and results for assigned protocols to meet country commitments. Contributes to the development of local SOPs.

WHAT MAKES THIS JOB SPECIA L?

  You will join a successful and stable project team: last year we almost doubled our team in France. If you come from a CRO environment, you´ll value being exposed to a rich interaction with internal client partners such as Finance, Med Affairs, Quality, Legal and Regional Operations, Head Quarter functional areas…   This is a pure customer-facing role, allowing you to build high-level business relationships, representing the sponsor to IRB/IECs and Regulatory Authorities, vendors and external partners to ensure country deliverables are obtained for submissions, budgets, CTRAs and local milestones   We have a well-organized structure, robust processes in place and unambiguous communication (you will know who to ask, will receive clear answers which will allow you to act fast)

OTHER INFORMATION

This role is a full time & permanent position to be employed through Covance. For more information please contact Carlos Villanueva on +34 648 853 615   or mail carlos.villanueva@covance.com

COVANCE ARE PRACTICING SOCIAL DISTANCING WITH VIDEO INTERVIEWS

All your interviews with us will be conducted via phone or using WebEx video. To help you prepare, check out this brief guide for best practices and WebEx guidance:

https://www.labcorp.com/labcorp-enterprise-video-interviewing-guide

  Education/Qualifications:

B.A./B.S. preferred in Business Finance/ Administration/ Life Science, or equivalent Health Care related experience Experience:You will have significant impact on how France deliver its country-specific trial commitments during study start-up, this is why we need you to bring a minimum of 5 years’ experience at a CRO or Bio-pharmaceutical company in start-up

   The position requires significant expertise in budget and contract negotiations, the local ethics, legislation and regulatory environment, submission and approval processes, development of local Informed Consent as well as other site ready and ongoing study deliverables. Ability to indirectly influence investigators, vendors, external partners and country managers to deliver these commitments is a must French and English