Study doctor (m/f/d)

Heidelberg University Hospital (UKHD) is one of the most important medical centers in Germany and stands for the development of innovative diagnostics and therapies as well as their rapid implementation for the patient. With around 14,000 employees throughout the group in more than 50 clinical departments with more than 2,500 beds, approximately 80,000 patients are treated in full and in part-stationary terms and more than 1,000,000 patients outpatiently.

Physician (d/m/w)

at the next possible time at the Klinik für Hämatologie, Onkologie und Rheumatologie (Innere Medizin V, Medical Director: Prof. Dr. C. Müller-Tidow) in the GMMG Study Group (Prof. Dr. H. Goldschmidt).

The therapy and research of multiple myeloma is a special focus of the Medical Clinic V (hematology, oncology and rheumatology). In the GMMG study group (German-Speaking Myeloma Multicenter Group), multicentric academic studies are coordinated and conducted with the “Multiples Myelom” indication. We offer a versatile, modernly equipped workplace and an interesting academic working environment.

Job ID: V000015242

Field of application: Department of Hematology, Oncology and Rheumatology

Location: Heidelberg

Start date: Next time

Field of activity: Medicine, Psychotherapy and Pharmacy

Type of employment: Full/ part-time (70-100 %)

Duration: limited (24 months)

Contract: TV-UK

medical advice from study teams on medical-scientific issues of study implementation and safety; Coordination in the study context. Self-employed Medical Data Review (medical examination of the study data, examination of the suitability of patients in screening, etc.) by reviewing, evaluating and checking the plausibility of study data according to the study protocol and regulatory requirements. Technical assessment of safety aspects and undesirable events in the study context: Medical assessment of serious adverse events (Second Assessment by medical staff). Review of Narratives and Creation of Security Reports. Regular consultation with the LKP. Participation in the design and development of clinical studies through the independent development and discussion of new study concepts. elaboration of scientific study reports, study reports and other study documents (e.g. Medical Review Plan, study-specific manuals). Training of non-medical and medical personnel in medical and study-regulatory matters: design and implementation of training for medical and non-medical study personnel on medical, methodical and study-regulatory issues in the context of clinical research. Responsible quality assurance by further developing and maintaining a quality management system in clinical trials in accordance with applicable guidelines and guidelines (ICH-GCP, AMG, MPDG).

Complete university studies of human medicine and medical approval Experience in the design, implementation and care of clinical trials of advantage Knowledge of ICH-GCP, Pharmaceutical Law and relevant national and international regulations Interest in the processing of scientific questions in clinical trials Good English knowledge of word and writing Team skills, motivation and commitment High level of responsibility

Work with most modern techniques / technical facilities Possibility of mobile work Flexible working hours as part of the sliding time Compensation by TV-UK E13, attractive occupational pension schemes 30 days off Continued: Jobticket (Germanyticket) Family-friendly work environment: cooperation on childcare, child-care allowance, advice for employees with a child-care...

Joblocations:

69120 Heidelberg, Neckar, Im Neuenheimer Feld 672, BADEN_WUERTTEMBERG, GERMANY