Activez les alertes d’offres d’emploi par e-mail !

Project Manager

Cromos™ Pharma

Paris

Sur place

EUR 50 000 - 70 000

Plein temps

Il y a 3 jours
Soyez parmi les premiers à postuler

Générez un CV personnalisé en quelques minutes

Décrochez un entretien et gagnez plus. En savoir plus

Repartez de zéro ou importez un CV existant

Résumé du poste

Cromos™ Pharma seeks a dedicated Manager to build and lead their clinical research team in Paris. This role focuses on promoting team performance, developing client relationships, and ensuring compliance with regulations while offering career development opportunities. Ideal candidates will possess managerial experience and a strong background in clinical trials.

Prestations

Competitive salary and benefits
Flexible working arrangements
Career opportunities at various levels
Support for personal development

Qualifications

  • Minimum two years managerial experience required.
  • At least two years in clinical trials.
  • Experience in ICH GCP Compliance essential.

Responsabilités

  • Lead a high-performing team and manage recruitment.
  • Coordinate local and remote project activities.
  • Develop patient recruitment strategies.

Connaissances

Leadership
Communication
Problem Solving
Client Relations
Proactivity

Formation

Degree in life sciences or medical sciences

Description du poste

Primary Location Europe
Job ID: PO_WA_CO_PM-1219
Job Type: Full-Time

JOB DESCRIPTION
Your main responsibilities:
  • Build a high-performing team by defining hiring needs, leading the hiring process, and managing a growing team;
  • Proactively identify market trends, new business development opportunities within the market and target customers;
  • Establish new customer relationships and maintain existing customer relationships;
  • Coordinate local project activities with Cromos team/PM managing multi-country studies;
  • Work with Corporate legal and finance to coordinate local legal and financial matters;
  • Participate in study site selection, including on-site and remote pre-study site evaluation visits and feasibility assessment activities;
  • Conduct monitoring activities, including on-site and remote monitoring visits and in-house monitoring activities between visits;
  • Assist in developing patient recruitment strategies with the project team and study sites;
  • Collaborate with and coordinate site investigators ensuring overall integrity of study and adherence to guidelines, protocol and regulations (both local country and overall governing body, as well as ICH GCP);
  • Perform and assist with project-specific administrative activities as a member of the project team.
  • Coordinate regulatory workflow, providing regulatory support to the team and tracking regulatory project timelines;
  • Collaborate with Cromos BD to assist in the performance of local country feasibility assessments, work with BD as requested and as part of the proposals team, if applicable.
  • Develop, together with Cromos Finance and BD, sales, revenue and expense budgets for the country and for performance in accordance with those budgets as well as other performance metrics for the local office.
You have:
  • Degree or postgraduate qualification in life sciences or medical sciences;
  • Strong ability to lead a team in order to advance team performance, health, and culture;
  • At least two years of proven managerial experience;
  • At least two years of clinical trials related experience (as investigator, CTA, IHCRA etc.);
  • Complete understanding of and experience in delivering in line with ICH GCP Compliance;
  • Excellent communication and presentation skills in English and local language;
  • Entrepreneurial mind-set: accustomed to seeking out commercially impactful partnerships;
  • Strong client focus and demonstrated experience in managing client relations;
  • Complete understanding of and experience in delivering in line with ICH GCP Compliance;
  • Proactivity and keen problem solving skills;
  • Understanding of financial metrics and productivity measurements;
  • Proven examples of decision making ability and ability to take initiative.
We offer:
  • Competitive salary and benefits;
  • Flexible working arrangements;
  • Career opportunities at local, regional and global levels;
  • Support for personal and professional development (trainings, coaching, career development, international assignments, etc).
If you are ready to start your journey at Cromos Pharma, please send your CV to cv@cromospharma.com.

Cromos Pharma is an international contract research organization delivering integrated clinical research solutions that accelerate drug development.

Obtenez votre examen gratuit et confidentiel de votre CV.
ou faites glisser et déposez un fichier PDF, DOC, DOCX, ODT ou PAGES jusqu’à 5 Mo.