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2.0 - 6.0 years
0 Lacs
hyderabad, all india
On-site
As a Regulatory Medical Writer-Clinical trials (RMW-CT), you are responsible for providing regulatory affairs (RA) strategic document expertise and support to one or more therapeutic areas (TAs) as designated by leadership. You will provide support for the preparation and submission of critical RA documents and responses to health authority (HA) or sponsor information requests using available reference materials such as documentation of previous interactions with HAs and sponsors, clinical development documentation, scientific literature, and content provided by sponsor teams. You may be the lead contact for sponsor or designated HAs interactions with cross-functional teams contributing to t...
Posted 5 days ago
2.0 - 6.0 years
0 Lacs
hyderabad, telangana
On-site
As a Regulatory Medical Writer-Clinical trials (RMW-CT), you are responsible for providing regulatory affairs (RA) strategic document expertise and support to one or more therapeutic areas (TAs) as designated by leadership. You will provide support for the preparation and submission of critical RA documents and responses to health authority (HA) or sponsor information requests using available reference materials such as documentation of previous interactions with HAs and sponsors, clinical development documentation, scientific literature, and content provided by sponsor teams. You may be the lead contact for sponsor or designated HAs interactions with cross-functional teams contributing to t...
Posted 2 months ago
0.0 - 4.0 years
0 Lacs
karnataka
On-site
Job Description: As a Medical Writing Associate at Teva Pharmaceuticals, you will play a crucial role in ensuring the accurate and timely completion of medical writing deliverables to support regulatory submissions and other clinical documents. Your responsibilities will include: - Writing, editing, and reviewing clinical study reports, protocols, investigator brochures, and other regulatory documents - Collaborating with cross-functional teams to ensure consistency and accuracy of scientific content - Ensuring compliance with regulatory guidelines and company standards for all medical writing deliverables Qualifications required for this role: - Bachelor's degree in Life Sciences, Pharmacy,...
Posted 3 months ago
1.0 - 5.0 years
0 Lacs
, India
On-site
About Strand Life Sciences: Strand is a 24 year old spin off from the Indian Institute of Science. We are a cutting edge Genomics company with a global customer base. We build applications that use DNA sequencing to improve human health. In the process, we build algorithms, data pipelines and visualizations to handle large amounts of sequence data. We anticipate that in the next few years, hundreds of millions of individuals will have their DNA sequenced, and invite you to join us in this transformative journey. About the Position: We are looking for scientists with a background in genetics, molecular biology, oncology or related areas with some exposure to omics data (genomics, proteomics, ...
Posted 5 months ago
3.0 - 7.0 years
0 Lacs
maharashtra
On-site
The job involves extracting relevant data from Chemistry related documents found on the internet and using this information to prepare Material Safety Data Sheets (MSDS). You should have a strong understanding of scientific literature, including journals and patents, and be able to apply this knowledge in Quality Control/Quality Assurance (QC/QA) and Research & Development (R&D) activities in the laboratory. It is essential to maintain the confidentiality of all information and be skilled in handling various chemical reactions and developing chemical analysis methods. This is a full-time position with opportunities for performance and yearly bonuses. The work location is in person, and the a...
Posted 5 months ago
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