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Job Details

Clinical Project Manager (m/w) Munich

Company: i-Pharm Consulting
Location: Germany
Reference: GA112017
Closing Date: 21 Nov 17
Type: Permanent
Salary (£): Negotiable

Job Summary:

Clinical Project Manager (m/w) Munich The main aim of the Clinical Project Manager (CPM) is the operational management of studies or projects managed by the company. ...


Clinical Project Manager (m/w) Munich

The main aim of the Clinical Project Manager (CPM) is the operational management of studies or projects managed by the company.

Essential Functions:
Perform operational management activities, from project/study start (pre-study phase) to project/study closure in a performance-oriented and timely manner within the budget
Manage Study Teams within the company in the area of clinical trials, clinical investigations, and other interventional or non-interventional studies, in adherence to Good Clinical Practice, international standards, and regulatory requirements
Responsible that milestones and timelines are met and services delivered
Responsible for the performance of the project/study with regards to the quality standards of the company and/or Sponsors/Clients wherever applicable
Responsible for the performance of the project with regards to budget adherence and resource allocation
Occasional clinical on-site monitoring may be required

Bachelor’s degree in a biomedical-related field, life sciences or equivalent field
Preferably about 3 years prior experience in clinical research
Experience as Clinical Research Associate (CRA) and Clinical Project Coordinator (CPC)
Preferably about 1 year prior employment-related experience in project scheduling, managing resources and coordinating team activities
Excellent oral and written communication skills in English
Demonstrates high level of organization, multi-tasking, judgement and analytical skills
Good time management skills to ensure adherence to timelines
Profound knowledge of Good Clinical Practice, 21 CFR Part 11, and other relevant regulatory requirements
Dedication to quality and reliability
Commitment to continuous training and knowledge sharing; proactively keeping up to date with procedural industry standards and international regulatory developments in clinical research
Ability to work well independently and as part of a team
Maintains confidentiality of project information
Computer literate
Attention to detail, tactful, and diplomatic
Possess adequate knowledge and experience to train, instruct and guide CPCs and CRAs
Possess a broad knowledge of clinical research methodology
Ability to represent the company at investigator meetings and monitor trainings

Apply for this job: Clinical Project Manager (m/w) Munich

Contact Information:

Address:  Head Office
212 New King’s Road London
Reasons to work for i-Pharm Consulting
Tel:  +44 (0) 20 3189 2299
Website:  Visit Our Web Site

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