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Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.
Associate Clinical Research Physician
Job ID R0000040322 Berlin, Land Berlin, GermanyWe are currently recruiting an Associate Clinical Research Physician to join our EPCU in Berlin! In this role you would act as co-investigator on phase I and II studies, ensure the safety of their trial participants at all times and support the Principal Investigator in preparation, organization, conduct and report of clinical trials according to protocol, Standard Operating Procedures (SOPs), ICH-GCP and local regulations. This role will be 32 hours per week and involves morning, afternoon and very occasional night shifts. Availability for weekend shifts is also desired, with durations depending on business needs.
Key Accountabilities:
Manage clinical trials:
Support responsible Principal Investigator and Deputy PI according to the national and international laws and all applicable guidelines.
Responsible for conduct of assigned studies.
Coordinate and support medical activities and medical responsibility.
Comply to German Drug Law, local law, study guidelines and SOPs for the studies being performed in the department.
Support duties relevant to the Medical Operations Department to ensure performance is met and or exceeded both for the business and own personal goals/objectives:
Participate in own Personal Development Process.
Process and data quality optimization.
Performance of the emergency training in Medical Operations.
Participate in medical/scientific discussions with sponsors in teleconference and meetings on study level.
Participate in interaction with external specialists and in Sponsor meetings during the course of studies as required.
Participate in the writing of medical reports, publications, SOPs and work instructions.
Maintain a positive, results orientated work environment, communicating to the team in an open, balanced and objective manner.
Skills:
Computer skills (MS office, MS outlook, etc.).
Good peer and patient relationship management.
Strong clinical and ethical problem-solving abilities.
Knowledge of clinical research, applicable German/European guidelines and laws and ICH GCP.
High interpersonal, verbal and written communication skills, superior English and German language skills (verbal and written) are mandatory.
Client focused approach to work.
A flexible attitude with respect to work assignments and new learning.
Ability to manage multiple and willing to prioritize workload with enthusiasm and attention to detail.
Advanced Life Support (ALS) trained and updated.
Education:
University degree as a medical doctor including approbation.
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