Indegene Pharma Scientific Writing Job Openings – Apply Now
Scientific Writer
Bengaluru, Karnataka, India
Hybrid Full-time Associate
About the job
We are a technology-led healthcare solutions provider, driven by our purpose to enable healthcare organizations to be future-ready. We offer accelerated, global growth opportunities for talent that is bold, industrious, and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship and is guided by passion, innovation, collaboration, and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out www.careers.indegene.com.
What if we told you that you can move to an exciting role in an entrepreneurial organization without the usual risks associated with it? We understand that you are looking for growth in your career at this point and would love for you to join us in our journey and grow with us. At Indegene, our roles come with the excitement you require at this stage of your career and the reliability you seek. We believe in creating leaders of tomorrow and mentoring our leads to help them grow and nurture them as people managers and account managers.
We are a rapidly growing global organization and are scouting for the best talent for this
phase of growth. With us, you are at the intersection of two of the most exciting industries: healthcare and technology. We offer global opportunities with fast-track careers while you work with a team fueled by purpose. The combination of this will lead to a truly differentiated experience for you.If this excites you, then apply below.
You will be responsible for:
- Review of promotional and medical communication materials (for various client products) and ensure the content in these materials is medically accurate, scientifically rigorous, truthful and balanced, relevant to product and therapy area, compliant to various pharma regulations and guidelines, and is supported by authentic and up-to-date references.
- Develop and update content for various medical materials, perform literature search to identify appropriate references to support creation/update of scientific content, track and audit assets for various purposes.
- Develop and review content for various deliverables meeting quality requirements as per client satisfaction metrics, within assigned timelines and with guidance from the manager. The tasks will be carried out as per assigned processes, guidelines, and SOPs with the help of tools and platforms specified by the client and the manager.
- Responsible for following the best practices in the department regarding processes, communication (internal & external), project management, documentation, and technical requirements like language, grammar, stylization, content search, summarizing, data conflicts, and referencing.
- Participate in assigned training programs and work on assignments as required.
- Participate in client calls as per project requirements.
- Compliance to quality, confidentiality, and security; adhere and follow quality systems, processes, and policies; comply with training and specifications.
Your impact:
About you:
- Prior work experience in the medical information domain (1-3 years) is required for this position.
Must have:
- Education—PharmD/MPharm/MD/MDS/PhD with Post Doc (or experience)/MBBS with experience.
- Minimum 1 to 4 years of experience in pharmaceutical companies.
- Understanding of any specialty area of medicine (preferred) or an overall understanding of the medical field.
- Strong flair and passion for writing.
- Strong written and verbal communication/presentation skills.
- Passion for networking.
- Being up to date with the latest technical/scientific developments and relating them to various projects.
- Client-oriented attitude with focus on creating strong long-term relationships with clients and encouraging others to work toward this goal.
- Ability to assure timely completion of assignments.
- Skilled in problem identification and problem solving.
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