Ph3Purpose /h3 pDevelop medical writing content within the pharmaceutical industry, collaborate in a matrixed, team environment, and apply internal standards, regulatory guidelines, and publishing guidelines to successfully deliver clinical documents. /p h3You will be responsible for /h3 ul liWriting and coordinating basic clinical documents such as Phase 1 protocols, Phase 1/2 CSRs, tables of studies, narratives, and initial investigative brochures. /li liContributing to and coordinating low‑to‑medium complexity clinical and regulatory documents, including Phase 2/3 CSRs and protocols, investigative brochure updates, summary documents, and regulatory responses under supervision. /li liPerforming document QC, completing lists of abbreviations or references, conducting literature searches, and other basic tasks with supervision as needed. /li liLeading cross‑functional document planning and review meetings and participating in process working groups. /li liManaging timelines and scheduling for assigned projects and interacting with cross‑functional colleagues to champion medical writing processes and best practices. /li liEstablishing document timelines and strategies in accordance with internal processes, with mentorship from functional management and clinical teams. /li liGuiding or training cross‑functional team members on processes and best practices. /li liLeading early‑or late‑stage compound writing teams with supervision, as required. /li liLearing and adhering to SOPs, templates, the Medical Writing Style Guide, and industry regulatory guidelines. /li liMeeting with managers and mentors, attending departmental and cross‑functional meetings, and completing time reporting, training, and metrics database updates. /li liMaintaining and applying knowledge of industry, company, and regulatory guidelines and mentoring junior staff on document planning, processes, content, or providing peer review. /li /ul h3Qualifications / Requirements /h3 ul liUniversity or college degree in a scientific discipline (advanced degree, such as Master’s, PhD, or MD, preferred). /li liMinimum of 2 years of relevant pharmaceutical or scientific experience. /li liMinimum of 2 to 4+ years of regulatory medical writing experience, depending on task complexity and supervision required. /li liStrong oral and written communication skills, attention to detail, and time‑management abilities. /li liAbility to work effectively in a team environment and grow learning agility. /li liDemonstrated ability to build solid, productive relationships with cross‑functional team members. /li liExperience interpreting, summarizing, and presenting statistical and medical information to ensure quality and accuracy of content. /li liEmerging leadership skills in project and process management, including influencing, negotiating, assertiveness, and initiative taking. /li liKnowledge of regulatory guidance documents such as ICH requirements. /li /ul h3Required Skills /h3 p— /p h3Preferred Skills /h3 ul liBusiness behavior, business writing, clinical research, and regulations /li liClinical trials operations, coaching, collaboration, copy editing /li liData gathering and analysis, data savvy, document management, industry analysis /li liMedical affairs, medical communications, problem solving, process oriented /li liProofreading, quality standards, research ethics /li /ul pLocation: Allschwil, Basel-Country, Switzerland /p /p #J-18808-Ljbffr