Senior Team Lead, Real-world Evidence Consulting - Paris, France - Cerner Corporation

Cerner Corporation

Entreprise vérifiée

Paris, France

il y a 3 semaines

Posté par:

Sophie Dupont

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Description

Cerner Enviza an Oracle Company is a leading global healthcare consulting firm and trusted advisor to many of the world's top pharmaceutical, biotech, and medical device & diagnostic companies.

By supporting the work of Cerner Enviza, you will work with world-class healthcare companies, helping them improve global access to medicines by connecting science and research.

Cerner Enviza is passionate about our people, our business, and our clients and is proud to foster a culture that contributes to the health and well-being of humankind

With ongoing and groundbreaking developments in Oncology and Rare Disease, an increased focus on more scientific, targeted medicine and continuous integration of technology into development and delivery of medicine, there has never been a more exciting time to work in Life Sciences and, with Cerner Enviza immersed in all of these, there has never been a better time to join us and make a difference to our clients and the lives of patients.
Thanks to our Business growth Cerner Enviza is looking for a new talented Senior Team Lead, Real-World Evidence Consulting (A). In this role, you will be a member of the Project Team for international studies. You will have an overall responsibility and accountability for the execution of the clinical operations strategy of the project, from sites selection to sites closure. The Senior Team Lead, Real-World Evidence Consulting (A) is responsible for coordinating and managing the clinical operations and local site services maintenance team, providing leadership and expertise to ensure successful execution of the site selection, clinical operations and regulatory maintenance project deliverables (quality, timeline, budget and scope).The Senior Team Lead, Real-World Evidence Consulting (A) will also manage a team of CTA.
This role requires collaboration within a matrix international environment, proactive internal and external communication, and exceptional strategic planning, risk management and organizational skills.
MISSION
Write the monitoring plan "Quality Review Plan";
Supervise, coordinate and lead the CRA's activity in several countries;
Proactively manage the client relationship kickoffs, results presentations, regular followup teleconferences, daytoday management in the course of projects life;
Ensure the fulfilment of objectives defined in the protocol (number of patients and centers, timelines, budget);
Ensure the ICH-GCP, corporate & local SOPs, and local regulations are respected and followed by all parties in every countries;
Select potential investigating centers according to their qualifications, clinical experience, research background and areas of expertise, in agreement with the Project Manager and the client;
Regular quality control of eTMF;
Monitor study progress: alert the project team, and make the necessary decisions and actions to solve any study related matter under your responsibility;
Managing site and suppliers' budgets;

People Management Responsibilities:

Delegate the work appropriately, provide clear expectations and follow up to ensure progress and overcome roadblocks. Identify associates and team priorities based on business direction and adjust when needed.
Lead by example and share knowledge and experiences with associates and team. Create a respectful work environment where you advocate for your team, create accountability and recognize accomplishments.
Provide timely feedback to encourage success, ensure accountability and connect opportunities for your associates' development.
Identify the right talent to achieve the desired results. Promote and build a diverse and cohesive team to accomplish objectives and align associates' skills to fill gaps.

Working Environment:

Hybrid or RemoteThis position offers a Hybrid or Remote working environment. Meaning if you live within a metro area of a Cerner office, you will split working time between a Cerner office and remote. If you are not within a metro area of a Cerner office, you can live and work in your current geographical location and work primarily remote. #LI-Hybrid #Remote

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Additional Information:

Working Environment

Hybrid or Remote
Relocation Assistance Available for this Job:
No
Qualifications:

Basic Qualifications:

Bachelor's Degree;
Min. 2 years of direct site monitoring experience in a bio/pharma./CRO;
Fluency English (C2);
In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines;
At least 1 year people management, matrix management, project management

All employees must be legally authorized to work in the country where the position is located. If applicant lacks required authorization, work visa sponsorship may be available for this position.

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