Vakante Jobangebote finden Sie unter Projekte.
Medical Writer Job
Eingestellt von Yoh
Gesuchte Skills: Client
Projektbeschreibung
WHAT YOU'LL BE DOING:
- Work directly with clinical study teams, the Oncology medical writing teams, regulatory affairs personnel, and the publishing group in the preparation of scientifically valid regulatory documents.
- Responsibilities include prepare regulatory documents on behalf in accordance with the ICH guidelines, international regulations, standards and processes, and the Writing Style Guide as applicable.
- Documents include but are not limited to: Protocols and protocol amendments, clinical study reports, Investigator brochures, and submission documents.
- Participate in project team meetings to provide input regarding deliverables, timelines, and processes.
- Responsible for managing the document review process.
- Route documents for approval.
- The medical writer should be familiar with ICH guidelines and the current AMA Style Manual.
- The writer will be expected to format and manage long documents with multiple review cycles and tight deadlines.
WHAT YOU NEED TO BRING TO THE TABLE:
- Bachelor's degree in life sciences, RN, Master's degree in life sciences, PharmD or PhD preferred.
- Would prefer full time onsite 5 days a week, however we will accept someone to work remotely but must work 2-3 days minimum onsite.
- Excellent writing skills, meticulous attention to detail, proficiency using an electronic document management system, and strong analytical ability to interpret clinical data.
- Experience: five (5+) years' writing experience in the pharmaceutical
OPPORTUNITY IS CALLING, APPLY NOW!
RECRUITER: Krista Leach
Yoh, a DayJ2W: HC; J2W: PROF
MONJOBJ2WMIDATL
Ref:
SFSF: LS
Projektdetails
-
Einsatzort:
Woodcliff Lake, Vereinigte Staaten
-
Projektbeginn:
asap
-
Projektdauer:
Keine Angabe
- Vertragsart:
-
Berufserfahrung:
Keine Angabe
Geforderte Qualifikationen
-
Kategorie:
IT Entwicklung