Clinical Research Physician (m/f)
Graduate job Biberach (Tübingen) IT development
Job description
Would you like to utilize your expert knowledge in clinical research and your passion to work on scientific concepts? If so, seize this opportunity and join us in Biberach/Germany as Clinical Research Physician (m/f)!
Job Profile
· As Clinical Research Physician you are responsible for planning, conduct and reporting of clinical trials
· You are the Leader of international and local trial team(s), including external partners
· You are responsible for the safety of study participants, including continuous monitoring of the benefit-risk ratio
· You ensure quality and data integrity on global and local level, as well as adherence to regulations and provide training
· With your medical expertise you ensure adequate medical understanding and oversight of individual trials and within the Oncology Group of Clinical Research Germany
· The co-ordination and contribution to preparation of trial documentation and authoring of the Clinical Trial Protocol belong to your further tasks
· You coordinate and oversee vendors, trial teams and external partners
· Furthermore you are responsible for development, oversight and control of trial budgets
· You also support local activities such as submission(s), investigator/site selection etc.
· You monitor compliance activities according to GCP, local regulations and adherence to trial protocol
· Continuous benefit-risk monitoring including regular medical and data quality review belong to your business
· You provide internal consultancy and advice on safety aspects within clinical trials
· Additionally you hold expert meetings on clinical development, trial design, endpoint selection etc.
Desired profile
Requirements
· You are a certified physician (M.D.) with special interest in Oncology and Hematology or comparable qualification
· You have sound medical knowledge of the disease under investigation, trial related risks, and understanding of the Investigational Medicinal Product, procedures and study design and their potential impact on patient's wellbeing
· You have a very good knowledge of regulatory landscape regarding clinical research, especially GCP, Declaration of Helsinki, European and US guidance
· You are characterized by your good scientific, medical and analytical thinking
· Furthermore you are fully and permanent aware of ethical responsibility inherent to research involving human subjects
· Your highly developed team leadership skills enable you to lead project teams in a matrix organization
· Fluency in written and spoken English and German is absolutely necessary
· A structured mind-set in the approach of complex tasks will be a plus
· You are also characterized by your excellent communication, interpersonal and social skills with very good time management
About Us
Boehringer Ingelheim is a research-driven pharmaceutical company and one of the top 20 pharmaceutical firms worldwide. Headquartered in Ingelheim, Germany, Boehringer Ingelheim operates globally in over 100 countries and has more than 47,700 employees. The focus of the family-owned company, founded in 1885, is researching, developing, manufacturing and marketing new medications of high therapeutic value for human and veterinary medicine. In 2014, Boehringer Ingelheim achieved net sales of about 13.3 billion euros. R&D expenditure corresponds to 23.1% of its net sales.
Contact
Boehringer Ingelheim is an equal opportunity employer who takes pride in maintaining a diverse and inclusive workplace. We embrace all aspects of diversity and inclusion which benefit our employees, patients and communities.
We look forward to receiving your online application in English - please enter the Job ID 40031645 BC 02/16 4 .