Project Manager (m/w/d)

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.

This project manager will ensure that clinical trials at PROFIL are conducted
on time, within the planned resources and with highest quality. Flexible
working hours and mobile working will be possible as soon as the
familiarisation and training into the new position is completed.

We are currently recruiting a

Project Manager (m/w/d)

Your responsibilities:

* Plan project goals and objectives
* Responsible for project communication, coordination and controlling
* Demonstrate a goal-oriented, trusting, flexible and motivating 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
Your profile:

* A Bachelor’s or an advanced degree in science (e g. biology,
chemistry etc.) would be beneficial
* Previous relevant experience in a CRO is mandatory, as well as experience
in clinical trial management and project management
* Empathetic, helpful personality who is proactive and focused on solutions
with a hands-on mentality
* Very good MS Office application skills
* Fluent English language skills are a must, German language skills are a plus
* Exceptional organizational and interpersonal skills
* Ability to work both independently and within a team setting to obtain
individual and company objectives
Our offer:

* We take pride in our company culture based on respectful, friendly and
positive interactions between all colleagues and between all levels
* An exciting role with deep insights into clinical research at top level
* In addition to flexible working hours, you can expect competitive pay with
an annual salary increase adjusted to the inflation
* Intensive induction into the job, comprehensive training on the job as well
as the opportunity for further development
* Bicycle leasing (also e-bikes) via the company Business Bike and free
charging possibility for ebikes
* Performance-related pay with annual inflation compensation and a secure job
with a permanent employment contract
Are you interested in this role?

Don’t hesitate to send us your CV, a motivation letter as well as
records of your qualifications/ employment reference letters via email,
preferably as pdfs, tohr@profil.com

.

APPLY HERE

Martin Schneider
Executive Director Human Resources
hr@profil.com

Profil Institut für Stoffwechselforschung GmbH
Hellersbergstraße 9, 41460 Neuss
www.profil.com