Medical Writer RWE (F/M)
Oracle
- France
- CDI
- Temps-plein
- Prepare manuscripts for publications and posters;
- Review statistical analysis plans and table/figure/listing specifications for appropriate content, and for grammar, format, and consistency;
- Act as a subject matter expert and medical/scientific advisor; main therapeutic areas: oncology and rare diseases;
- Mentor junior medical writers;
- Work on a variety of projects at the same time;
- Work effectively with other teams in Oracle Life Sciences, particularly Data Management and Statistics Teams;
- Ensure projects are delivered to time and budget;
- Bachelor's Degree or equivalent in a relevant scientific field, higher degrees (PhD/MSc) preferred;
- You have a strong writing experience within a pharmaceutical company or CRO, with a focus on the writing of protocols and study reports according to ICH guidelines and preparation of manuscripts for publication. (comparable to 3+ years’);
- Fluency English (C2);
- Intellectual curiosity and creativity;
- Excellent communication skills – able to distill issues, manage client expectations and act as a trusted advisor in a timely manner;
- Excellent planning, organization skills;
- Ability to work effectively in a team in a fast-paced and dynamic environment;
- Able to manage multiple priorities, work efficiently under pressure and consistently meet tight deadlines;
- Flexibility and agility with changing priorities and timelines;
- A first experience with patient-centric studies, namely Epi. Studies, HEOR, Patient Reported Outcomes (PRO) studies will be a plus;
- A first experience or knowledge of databases - SDNS, CPRD, JMDC; MarketScan, Optum -, in any of the major markets (EU-5, Japan, US, Israel, etc.) will be a plus.
- Which includes being a United States Affirmative Action Employer