14 Dec

Clinical Project Manager Jobs Vacancy at Key People

Position
Clinical Project Manager
Company
Key People
Location
Opening
14 Dec, 2017 30+ days ago

Key People urgently required following position for Clinical Project Manager. Please read this job advertisement carefully before apply. There are some qualifications, experience and skills requirement that the employers require. Does your career history fit these requirements? Ensure you understand the role you are applying for and that it is suited to your skills and qualifications.

Follow the online directions, complete all the necessary fields, and provide all relevant information so your application is submitted correctly. When you click the 'Apply this Job' button (open in new window) you will be taken to the online application form. Here you will be asked to provide personal and contact details, respond to employment-related questions, and show how you meet the key selection criteria.

Clinical Project Manager Jobs Vacancy at Key People Jobs Details:

We are searching for an International Clinical Project Manager to work for our global pharmaceutical client based in Switzerland. Main responsibilities: 1. Support Programme Manager in ensuring all trial deliverables are met according to timelines, budget, operational procedures and quality standards. Assigned responsibilities can include development of specific sections of protocol and related documents; development of study tools, guidelines, and training materials; management of clinical study material; and implementation of issue resolution plans. 2. Support Programme Manager in preparation of clinical outsourcing specifications and in the follow-up with day to day operational activities with the Contract Research Organization(s) (CROs). 3. Support Programme Manager in managing interactions with Global Clinical Development Operations and other relevant functions including Drug Supply Management and company local medical organizations. 4. Update regularly all trial information databases and tracking systems in order to manage accuracy of information. 5. Contribute to the ongoing scientific review of the clinical trial data during the course of the trial. 6. Support Programme Manager in delegated aspects of trial data analysis and reporting. 7. May assist in program level activities (e.g., tracking of CD&MA brand-related publications, development of clinical sections of regulatory documents like Investigators' Brochures, briefing books Requirements: Education: ? Bachelor degree or equivalent education/degree in life science/healthcare is required accompanied by ?4 years of involvement with clinical study planning, execution, reporting and publishing activities (either at a local medical organization, investigational site, pharmaceutical company/CRO, or clinical fellowship program).


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