Receptionist (m/f)

For classical duties at the company reception desk and receipt of incoming company phone calls. You will be expected to handle incoming and outgoing post, receive visitors, prepare for meetings both national and international including the coordination of refreshments, organise employee travel arrangements, manage finances for cash purchases, manage and update the international company telephone list and occasional special projects.

You have a pleasant and business demeanour, your oral and written expressions are excellent, you have a good working knowledge of MS-Office applications, you are service oriented and you have a talent for organisation. Your oral and written English and German is good and you have a sense of humour, work well in a team and gain satisfaction from your work. Preferably, you already have experience in this position.

Admin dept

Munich, Germany

Business Development Associate

The Business Development Associate will be responsible for acquisitions and client care and for the  supervision and administration of a clinical trial project from the client information request to the signing of a contract. You will be involved in the preparation of cost offers and proposals and you enjoy dealing with numbers, you have strong communication skills, good knowledge of MS-Office applications, especially Excel, good team building skills and excellent written and spoken English and German. Candidates must be able to work independently to high standards, have the capacity to plan and set priorities and be able to manage time well.
Previous experience in clinical research or a medical or legal background would be a definite advantage.

BD dept

Munich, Germany

Assistant Business Development

The Assistant Business Development will assist the Business Developmemt team with the administration of clinical trial project from client information request to signing of a contract.
Candidates must have good oral and written English and German, good communication skills and be able to work well in a team and also be self-reliant. Experience with MS-Office applications is a must and previous experience in clinical research/medical or legal positions would be useful.

BD dept

Munich, Germany

Doctors Assistant

You are a qualified Doctors Assistant and are looking for a Monday to Friday job of 40 hrs per week. You are prepared to be flexibly assigned to different tasks in our clinical unit, e.g. assistance during the carrying out of clinical studies (blood sampling, laboratory analysis), assistance in the service centre (telephone calls to and from volunteers for appointment scheduling), helping the catering team, coordination of study data ( PC coordination of central study time plan, data-entry, data archiving and the documentation that these tasks generate).
We require someone with a talent for organisation and who is reliable and a team player. You have good English and German both spoken and written and a good working knowledge of MS-Office applications.

Clinical Operations dept

Medical Project Leader

You will be responsible for the medical site management of 10 study centres in Germany. This will involve central coordination and management of the study centre medical personnel, helping to recruit the relevant study teams in the towns concerned, responsibility for the instruction and training of the study teams, being the central person for questions and problems that arise during the study and also the main contact person for the sponsor. You will also be expected to function occasionally as clinical study investigator for other clinical studies running from our clinical unit in Munich. This will sometimes involve working shifts at weekends or overnight.
The multi-centre study will run for 5 years, starting in January 2009. For the first 3-4 months this will be a full time job and thereafter there will be full-time periods of 4-6 weeks, every 6 months.Between the half yearly periods there will be minimal activity.
You are a qualified medical doctor with organisational talent and a flair for analytical, conceptional and communicative thinking. You are familiar with the provisions of ICH-GCP and you are used to working independently and responsibly. You have very good English and German, both spoken and written.

Clinical Operations dept

Clinical Data Assistant (part/full-time)
For our Biometrics dept we are looking for a part or full-time Clinical Data Assistant, to handle data from national and international clinical phase I-IV studies. You will be responsible for data entry and checking the correctness of data entry, organisation  and coordination of data analysis, compilation of data queries, coding of medical terms e.g. during adverse events, archiving of study data and relevant contact with our subsidiaries, study monitors, clinical investigators and sponsors.

You are a qualified Medical Documention Assistant or Doctor's assistant and you are absolutely reliable and meticulous with good organisational talent and verbal skills. You have comprehensive computer experience, especially in MS-Office applications and you have very good knowledge of English and German, both spoken and written.

Biometrics dept

Munich, Germany

Experienced Clinical Research Associates
With experience in international clinical studies. Duties will include investigator recruitment, regulatory submissions, pre-study, initiation, routine and final monitoring visits, mainly in Germany. You have a background in the life sciences or medicine and you have good English and German both written and spoken and a good knowledge of MS-Office applications. You have the ability to work independently as well as communicating and interacting well with the project manager and team.

Clinical Research

Munich, Germany

Experienced Field Based CRAs

We require field based CRAs with experience in international clinical studies, for the areas Germany south west, Germany west, Germany east and Germany north. Duties will include investigator recruitment, regulatory submissions, pre-study, initiation, routine and final monitoring visits, mainly in Germany. You have a background in the life sciences or medicine and you have good English both written and spoken and a good knowledge of MS-Office applications. You have the ability to work independently as well as communicating and interacting well with the project manager and team.

Clinical Operations

Clinical Trials Administrator
You are a life sciences graduate, MTA, PTA or doctor's assistant. As CTA you will be responsible for the project related preparation, collection and tracking of all study data and documentation and you will provide support to all functions in Clinical Operations and assist PMs and CRAs with their project related activities. This will include setting up of systems for study conduct and handling and archiving all correspondance, study data and documentation and the preparation of status reports for sponsors.

Experience in the CRO or health care industry, as a CTA or project assistant, would be an advantage but is not essential. Fluency in German and a good working knowledge of English, both oral and written, good proof readng skills and a good knowledge of medical terminology are essential as would computer experience (Word, Excel, PPT). You have the ability to coordinate and prioritise, you have a good eye for detail and you are a good team player.

Clinical Operations

Munich, Germany

Clinical Investigator (m/f)
You will be responsible on a freelance basis for the planning and conduction of clinical studies. This includes competent medical and scientific consultancy to our clients and our clinical dept.
You are a qualified medical doctor with experience in internal medicine, anaesthesia, or general medicine. Preferably, you also have experience in  a specialist area such as pulmonology, cardiology, diabetology, or pharmacology and experience in the planning and conduction of clinical studies as an investigator.
We expect you to be familiar with the requirements of ICH-GCP and the German AMG and to be able to work independently, conscientiously and with organisational flair. You have excellent written and spoken English and German and you are familiar with MS-Office.

Clinical Research

Munich, Germany