Job Summary For one of the Top 4 global players in the pharmaceutical industry DOCS is hiring a CQM Coordinator (m/f) in Germany/Darmstadt. If you like to get a foot in the door of one of the big players in pharma and work in a very international environment, this might be for you! Roles & Responsibilities of the position Support the SOP review process and revision of documents • Communicate and align with SOP authors and contributors within and outside of the department • Set-up SOP process graphs (iGrafx) • Distribute Quality Documents into review • Revise documents to comply with consistency standards and format requirements • Schedule SOP review follow-up calls Support Compliance Oversight • Track Compliance (Training, CAPA) measures and support reporting • Interact and follow-up with stakeholders to ensure timelines are met Job Requirements • Experience in clinical research in a CRO, pharma or biotech company • Organized and able to structure • Experience in document management and thorough work style • Flexibility and adaptability • iGrafx experience a plus • Good interpersonal skills • Demonstrated good written and verbal communication skills • Fluency in English (oral and written), German is a plus Remuneration & other details • 12 months contract with DOCS with chance for extension or perm • Chance to work for one of the leading sponsors • Full time, office based in Frankfurt area. An office/home office mix is possible after some time • Great pipeline of studies -> very good long term perspective • Top 4 global player in the pharmaceutical industry • Company pension scheme Why this vacancy is right for you: We offer an exciting and challenging work environment for clinical research professionals looking for an opportunity to contribute to the success of a company dedicated to researching, developing, manufacturing and marketing pharmaceuticals that improve health and quality of life. Interested? Please submit your CV to or call me on (0) . We are looking forward to your application.