All roles

Expert Scientific Writer

Remote · USA Full-time New today

Job Description Summary

Creation of high-quality complex scientific content, such as publications and foundational core content elements, in line with priorities and scientific narrative defined in SCP. Ownership of content from brief to publication or presentation, for first-time right delivery.

Job Description

Major Activities 

  • Demonstrate a command of assigned therapeutic areas and expertise with assigned products. 

  • Research and write original content for publications activities (primary and review manuscripts, abstracts, posters), slide presentations and other materials. 

  • Prepare meeting materials for satellite symposia (agenda, slide content, speaker briefings etc), and reports from advisory boards and other internal or external meetings. 

  • Develop content that is scientifically accurate, evidence-based, grammatically accurate, referenced using appropriate sources, and consistent with quality standards for author review, customer review as appropriate, and scientific peer review. 

  • Perform internal scientific reviews to ensure quality in line with the scope and scientific messages. 

  • Mentor internal team members and help onboard new joiners. 

  • As needed, perform quality control (QC) checking / proof reading of the above-mentioned documents to meet stakeholder expectations. 

  • Clearly communicate medical scientific concepts in a condensed, audience-appropriate way.  

  • Follow all internal processes and procedures with regard to workflow, development of deliverables, and adherence to industry best practices, including GPP. 

  • Demonstrate the flexibility/adaptability necessary to function on different therapeutic teams as needed and to work on projects across multiple brands at any given time. 

  • Provide input and aid in troubleshooting/problem-solving. 

  • Participate in strategic and tactical publications planning and related research. 

  • Maintains records for all assigned projects including archiving in line with global SOPs 

  • Maintains audit, SOP and training compliance. 

  • Performs additional tasks as assigned.   

Key Performance Indicators 

  • Adheres to quality, compliance to SOPs, timeliness, and productivity of deliverables as per KPI targets. 

  • Adheres to Novartis values and behaviors. 

Skills Desired

Clinical Research, Clinical Trials, Detail-Oriented, Medical Writing, Regulatory Compliance, Safety Apply To This Job

Related roles

Associate Director, Learning Innovation-Remote

Remote · USA Full-time

Associate Director, Market Access Portfolio Strategy

Remote · USA Full-time

Sovellusarkkitehti

Remote · USA Full-time

Data Scientist

Remote · USA Full-time

Business Development Director - Aftermarket Services – EMEA (Remote - Europe))

Remote · USA Full-time

Preventative Maintenance Technician

Remote · USA Full-time

Area Leader (Manager) Trainee - Franchise Operations

Remote · USA Full-time

Area Leader (Manager) Trainee - Franchise Operations

Remote · USA Full-time

Area Leader (Manager) Trainee – Franchise Operations

Remote · USA Full-time

Senior Technical Manager (Tax & Trusts)

Remote · USA Full-time

Pharmacist - Specialty Mail Order (Hybrid Work From Home)

Remote · USA Full-time

Urgently Hiring: Seasonal Package Delivery Driver

Remote · USA Full-time

Mobile Software Developer

Remote · USA Full-time

Live Chat Remote Data Entry Specialist – Amazon E-commerce Operations

Remote · USA Full-time

North American BDR Needed for New Services Platform - Contract to Hire

Remote · USA Full-time

Pharmaberater*in Impfstoffe (m/w/d) - Flensburg, Heide, Kiel

Remote · USA Full-time

Looking for Learning Center Assistant Director in Waldorf, MD

Remote · USA Full-time

[Remote/WFM] Sr. Account Executive, PubSec EDU - Higher Ed ENT

Remote · USA Full-time

Territory Manager - Tennessee (Nashville, Knoxville)

Remote · USA Full-time

Sr. Clinical Quality Auditor- Shockwave Medical (Remote)

Remote · USA Full-time