Project Manager (m/w/d)

at  Profil Institut fr Stoffwechselforschung GmbH

41460 Neuss, Nordrhein-Westfalen, Germany -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate11 Feb, 2025Not Specified12 Nov, 2024N/AGood communication skillsNoNo
Add to Wishlist Apply All Jobs
Required Visa Status:
CitizenGC
US CitizenStudent Visa
H1BCPT
OPTH4 Spouse of H1B
GC Green Card
Employment Type:
Full TimePart Time
PermanentIndependent - 1099
Contract – W2C2H Independent
C2H W2Contract – Corp 2 Corp
Contract to Hire – Corp 2 Corp

Description:

Profil is an internationally renowned CRO in the field of metabolic diseases, founded in 1999. For many years, we have been working closely with the pharmaceutical industry to develop new drugs for the treatment of diabetes and related diseases. We also intensively support the further development of known active substances. Furthermore, we conduct vital research regarding various other exciting applications such as novel routes of insulin administration or the measurement of blood glucose concentrations. Our many years of experience have enabled us to build up comprehensive scientific know-how and a unique expertise in the field of metabolic diseases. Profil currently employs around 330 people who make an important contribution to improving the quality of life of people with diabetes.
We are currently recruiting a
Project Manager (m/f/d)

Responsibilities:

  • Plan project goals and objectives
  • Responsible for project communication, coordination and controlling
  • Demonstrate a goal-oriented, trusting, flexible and motivativing project work
  • First point of contact for Sponsors, third-party organizations as well as internal interfaces
  • Organize, lead and document Sponsor oversight meetings and study handover meetings
  • Schedule and facilitate site-initiation visits
  • Support cross-departmental communication, problem solving and decision-making
  • Create Project Management Plans outlining tasks, milestones and required resources
  • Maintain and control project timelines
  • Report weekly project status updates
  • Plan and coordinate clinical trial submission preparations
  • Take responsibility for eTMF set-up and maintenance
  • Manage project risks and issues
  • Monitor project Key Performance Indicators
  • Controlling of planned project hours
  • Controlling of project access rights and training requirements


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Site Engineering / Project Management

Clinical Pharmacy

Graduate

Proficient

1

41460 Neuss, Germany