Study Manager/Clinical Team Manager - Munich or Hamburg

München
08.12.2019

Daten dieser Anzeige

Study Manager/Clinical Team Manager - Munich or Hamburg

Germany

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Job Description - Study Manager/Clinical Team Manager - Munich or Hamburg (165094)

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Job Description 

Study Manager/Clinical Team Manager - Munich or Hamburg - 165094

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Description

PPD has an exciting opportunity for a Clinical Team Manager (CTM) join us onsite exclusively for one of our strategic pharmaceutical partners in Munich or Hamburg, Germany. 

PPD works in collaboration with this partner; you will be dedicated to the client projects and sites, working within their teams, systems and processes on behalf of PPD. 

This is a great opportunity for study managers or those with relative experience working within the life science sector for pharmaceutical, biotech companies or CRO’s industry who would enjoy the opportunity to work for a CRO dedicated to one client.  

The role coordinates all aspects of local study management.  Responsible for the local implementation of international clinical trials and / or local trials entrusted to them, their preparation for their closure, in compliance with GCP, regulatory requirements, SOPs, quality standards, deadlines and costs.

This could include oversight of the Clinical Research Associates who are allocated to a project on a Country basis. You will work in partnership with the Project Manager to ensure the necessary training, tracking and quality systems are in place for the clinical team and be primarily responsible for the clinical deliverables of the project within agreed timelines and budget. Clinical Team Managers provide contact and support to the project sponsor for all clinical aspects.

We are seeking high performing individuals who enjoy a fast-paced environment and have had Clinical Management experience OR exposure to international or local studies, involving the coordination of CRAs locally and potentially across different countries. With your excellent written and oral English and German skills you will have exceptional interpersonal and problem-solving skills, with the ability to lead CRAs in different countries. You will also have proficient working knowledge of GCP and experience in several medical / therapeutic areas. You must be comfortable working in a matrix management system and have the ability to motivate, mentor and integrate teams.

We are seeking highly motivated and skilled applicants who will want to share in our continued growth in the international market place. We will consider field-based applicants depending on your experience level.

PPD is a leading global Contract Research Organisation  providing comprehensive, integrated drug development, laboratory  and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 47 countries and approximately 23,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a firm commitment to quality to help clients and partners bend the cost and time curve of drug development to deliver life-changing therapies that improve health.

*LI-SH1

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Qualifications

Education and Experience:

  • Bachelor’s degree or licenced certified health care training or equivalent combination of education and experience.
  • Clinical research experience in all phases of study life cycle, including start up, interim and close out.
  • Equivalent combination of education, training, and experience that provides the individual with the required knowledge, skills, and abilities.
  • Valid Driver’s Licence.
  • Valid Passport.

Knowledge, Skills and Abilities:

  • Superior organizational skills.
  • Demonstrated performance management abilities.
  • Extensive monitoring experience.
  • Excellent judgment and decision making skills.
  • Effective oral and written communication skills.
  • Excellent interpersonal skills and problem solving ability.
  • Ability to motivate and integrate teams and teach/mentor team members.
  • Able to effectively prioritize workload.
  • Strong attention to detail.
  • knowledge of relevant regulations e.g. ICH/GCP, FDA guidelines, etc

Organization

 - Clinical Monitoring

Primary Location

 - DE-DE-Munich-FSP Munich DE Prince Regent Sq

Sekretariat/ Assistenz/ Sachbearbeitung

Hauswirtschaft/ Au-Pair

Sonstige Branchen

Bereichs-/ Abteilungs-/ Gruppenleitung

München