Medical Writer (m/f/d) (Freelancer)


Your tasks:

    1. Generation of non-clinical and clinical documents (study reports, study protocols, investigator’s brochures, biomarker reports) and manuscripts for scientific publications
    2. Quality control of documents
    3. Close cooperation with other medical writers, statisticians, and project managers both within the company and on the client’s side
    4. Organization/planning of trial team meetings

Your profile:


    1. Education to an advanced degree level in a life science, medicine, or veterinary medicine discipline
    2. At least 3 years of professional experience as a medical writer in clinical research
    3. Knowledge in statistical evaluation of research results
    4. Thorough understanding of ICH, GCP, and other relevant guidelines and regulations
    5. Experience in literature research
    6. Excellent editorial and proofreading skills
    7. Ability to work in a team and a high degree of initiative
    8. Communication skills with fluency in the English and German language both

Statistician (m/f/d)


Job Profile:

  1. Statistical planning of clinical studies
  2. Generation of statistical analysis plans
  3. Statistical analysis and reporting
  4. Programming and validation of analysis programs
  5. Participation in the development and implementation of statistical methods and tools for data analysis.



  1. University degree (PhD/MSc) in Statistics or Mathematics
  2. Comprehensive knowledge of biostatistics with regard to study design and analysis
  3. Practical experience in clinical development
  4. Comprehensive knowledge in the application of statistical software solutions (SAS)
  5. Proficiency in English
  6. Self‐motivated, good communicator and team player.

Data Manager (m/f/d)


Job Profile:

    1. Generation of essential study documents like data management plan and data validation plan
    2. Set-up of clinical study data bases and validation
    3. Programming of consistency and plausibility checks
    4. Query management
    5. Development of paper and eCRF
    6. Validation of programs, data base audits
    7. Generation of CDISC/SDTM files
    8. Participation in the development and implementation of data management processes



    1. University degree (PhD/MSc) in Mathematics, Statistics or Natural Science or certified in medical documentation
    2. Comprehensive knowledge of data management in clinical studies
    3. Practical experience with data management in clinical studies
    4. Practical experience with CDISC
    5. Comprehensive knowledge in SAS
    6. Proficiency in English
    7. Self-motivated, good communicator and team player.
We offer excellent opportunities for professional and personal development, flexible office hours and part-time models.

Please send your application to:  M.A.R.C.O. GmbH & Co. KG:

M.A.R.C.O. GmbH & Co. KG
Personnel office
Schirmerstr. 71
40211 Duesseldorf

or E-Mail: