Scientific Writing Jobs at Johnson & Johnson
Are you passionate about scientific writing and ready to make a difference in healthcare? A rare chance has emerged for aspiring professionals in scientific writing at Johnson & Johnson in Hyderabad. The Hybrid Scientific Writing Jobs role is ideal for individuals with a scientific background, particularly those holding advanced degrees, who are eager to contribute to innovative healthcare solutions. As a Scientific Writing and Reporting Scientist, you will play a crucial role in advancing medical research. Interested candidates are encouraged to apply promptly.
About Johnson & Johnson:
Johnson & Johnson is a global leader in healthcare innovation, dedicated to improving health outcomes through advanced medical solutions. The company operates across various sectors, including pharmaceuticals, medical devices, and consumer health products. With a commitment to diversity and inclusion, Johnson & Johnson fosters an environment that respects individual contributions and promotes collaboration among its workforce.
Job Details:
- Job title: Scientific Writing and Reporting Scientist – Hyderabad
- Function: Discovery & Pre-Clinical/Clinical Development
- Sub function: Pharmacokinetics & Pharmacometrics
- Category: Scientist, Pharmacokinetics & Pharmacometrics (ST4 – E24)
- Location: Hyderabad / India
- Requisition number: R-094944
- Work pattern: Hybrid Work
Job Description:
The Clinical Pharmacology & Pharmacometrics (CPP) Scientific Writing & Reporting (SWR) Scientist is responsible for writing documents, coordinating reviews and document finalization, performing document quality control (QC), and managing timelines, resources, and metrics related to Clinical Pharmacology trials. They assist in the preparation of activities in support of Clinical Pharmacology Phase 1 studies, including protocol authoring and CSR writing. Additional responsibilities include QC review of documents and liaising with stakeholders to ensure timely and high-quality delivery of documents.
Key Responsibilities:
- Authors, coordinates, and facilitates timely reviews and approval of Phase I clinical and regulatory documents.
- Attends cross-functional document planning and review meetings, interacting with various stakeholders on document content in the Non-Clinical Job.
- Functions as the Phase I writer on compounds across all therapeutic areas under supervision.
- Performs QC of protocols and CSRs of Phase I clinical and regulatory documents.
- Learns and adheres to SOPs, templates, and regulatory guidelines.
- May participate in process working groups for writing processes within CPP.
- Completes all time reporting and training as required in relevant company systems.
Eligibility Criteria for the Hybrid Scientific Writing Jobs:
- A university/college degree in a scientific discipline is required; an advanced degree (e.g., Masters, PhD, MD) is preferred.
Required Skills for the Hybrid Scientific Writing Jobs:
- Proficiency in written and spoken English.
- Good technical skills with MS Word.
- Desire to learn how to interpret, summarize, and present statistical and medical information.
- Attention to detail, proficient in time and project management.
- Ability to build and maintain solid relationships with cross-functional team members.
