Consultant / Sr.Consultant - Scientific Writer Golden Opportunities

3.0 - 7.0 years

0 Lacs

pune, maharashtra

On-site

The role of Consultant / Sr. Consultant - Scientific Writer involves preparing literature reviews, abstracts, posters, slide sets, and manuscripts (complex) by working with various data sources such as clinical study reports and patient profiles. You will be responsible for performing quality control (QC) checks and proofreading of the deliverables to ensure they meet customer expectations. It is essential to comply with and support the group's project management tools, standards, policies, and initiatives. Maintaining records for all assigned projects, including archiving, and ensuring audit, SOP, and training compliance are also key responsibilities. The ideal candidate should have expertise in literature review, abstracts, posters, slide sets, and manuscripts. Attention to detail and the ability to meet customer expectations are crucial for this role. This is a full-time, permanent position in the ITES/BPO/KPO industry under the functional area of Pharmaceuticals. The role falls under the outsourcing/Offshoring category. If you have a passion for scientific writing and possess the necessary skills in literature review, abstracts, posters, slide sets, and manuscripts, we encourage you to apply for this position. Job Code: GO/JC/21340/2025 Recruiter Name: Mithra D,

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Senior Scientific Writer II Novartis India

2.0 - 8.0 years

0 Lacs

hyderabad, telangana

On-site

You will be responsible for writing, supporting, and managing projects to create high-quality medical and scientific communications, such as literature reviews, abstracts, posters, slide sets, and complex manuscripts for publication or presentation at congresses or to internal medical and clinical teams. You will work from various data sources, including clinical study reports and patient profiles, to prepare these deliverables. Additionally, you will perform quality control checks and proofreading to ensure the final outputs meet customer expectations. You will manage multiple projects simultaneously, focusing on up to two brands at a time. Gathering feedback from customers and implementing customer management tactics will be an essential part of your role. You will also adhere to project management tools, standards, policies, and initiatives set by the organization. Following Novartis specifications for documentation, including Novstyle and templates, is crucial, as is tracking clinical trial milestones for assigned projects. Keeping records for all projects, including archiving, and ensuring audit, SOP, and training compliance are key responsibilities. You will be expected to train new colleagues when necessary and take on additional tasks as assigned. To qualify for this role, you should have a minimum of a Science degree or equivalent, with 8 years of Clinical Research (CR) experience for B.Sc. or equivalent, or 6 years of CR experience for M.Sc./M.Pharm. Desired qualifications include a Doctoral Degree or Qualification in Medical Sciences (MBBS/MD/equivalent), or a PhD with 4 years of CR experience, MBBS/equivalent with 4 years of CR experience, or MD with 2 years of CR experience. Novartis is committed to creating an inclusive work environment and diverse teams that reflect the patients and communities served. Joining Novartis means being part of a mission to reimagine medicine and improve lives. To learn more about Novartis and explore career opportunities, visit: https://www.novartis.com/about/strategy/people-and-culture For information on benefits and rewards offered at Novartis, refer to the Novartis Life Handbook: https://www.novartis.com/careers/benefits-rewards. If you are interested in staying connected and learning about future career opportunities at Novartis, join the Novartis Network here: https://talentnetwork.novartis.com/network.,

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The cleaned title from the provided string is Scientific Writer . Golden Opportunities

2.0 - 6.0 years

0 Lacs

pune, maharashtra

On-site

The job involves preparing literature review, abstracts, posters, slide sets, and manuscripts from various data sources such as clinical study reports and patient profiles. Quality control and proofreading of deliverables are essential to meet customer expectations. Adherence to project management tools, standards, policies, and initiatives is required. Record-keeping for projects and compliance with auditing, SOP, and training are key responsibilities. The role is for a Consultant / Sr. Consultant - Scientific Writer in the Pharmaceutical industry. It is a full-time, permanent position in the outsourcing/Offshoring category. The key skills include literature review, abstracts, posters, slide sets, and manuscripts. Job Code: GO/JC/21340/2025 Recruiter Name: Mithra D,

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