Bangalore
2 years ago
13 Applied
JOB ID:44009
Job details
Job Type
Full Time
Functional Area
Content Writer/Editor/Journalist
Industry
Pharma/Biotech/Clinical Research
Education
Not Specified
Experience Required
4 - 6 Yrs
Key Skills Required
content writing
Other Skills Required
Languages
English
Job Description
Job Description- Senior Associate Scientific Writing
1. Develop content for MedInfo documents and develop clinical trial summaries meeting quality requirements as per client satisfaction metrics, with active guidance from the manager
2.Responsible to develop and review content for MedInfo documents and other scientific communication deliverables as per the timelines assigned
3.Should be able to perform literature search on any given topic on different databases like PubMed and Embase
4.Responsible to follow 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
5.Responsible for grooming and mentoring juniors in improving writing
6.Participate in assigned training programs and work on assignments as per requirement
7.Participate in client calls as per project requirements
8. Compliance to qualit... See More
1. Develop content for MedInfo documents and develop clinical trial summaries meeting quality requirements as per client satisfaction metrics, with active guidance from the manager
2.Responsible to develop and review content for MedInfo documents and other scientific communication deliverables as per the timelines assigned
3.Should be able to perform literature search on any given topic on different databases like PubMed and Embase
4.Responsible to follow 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
5.Responsible for grooming and mentoring juniors in improving writing
6.Participate in assigned training programs and work on assignments as per requirement
7.Participate in client calls as per project requirements
8. Compliance to qualit... See More
Job Description- Senior Associate Scientific Writing
1. Develop content for MedInfo documents and develop clinical trial summaries meeting quality requirements as per client satisfaction metrics, with active guidance from the manager
2.Responsible to develop and review content for MedInfo documents and other scientific communication deliverables as per the timelines assigned
3.Should be able to perform literature search on any given topic on different databases like PubMed and Embase
4.Responsible to follow 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
5.Responsible for grooming and mentoring juniors in improving writing
6.Participate in assigned training programs and work on assignments as per requirement
7.Participate in client calls as per project requirements
8. Compliance to quality, confidentiality and security:
9.Adhere and follow quality systems, processes and policies
10. Comply to training and specifications
Desired Profile:
1. Minimum4 to 6 years of experience in pharmaceutical companies - clinical research
2. Understanding of any specialty area of medicine (preferred) or an overall understanding of the medical field.
3. Strong flair and passion for writing.
4. Strong written and verbal communication/presentation skills.
5. Passion for networking.
6. Being up-to-date with the latest technical/scientific developments and relating them to various projects.
Education Qualification
M. Pharm/ Pharm. D/ BDS / MDS/Ph.D./ Any life science graduate See Less
1. Develop content for MedInfo documents and develop clinical trial summaries meeting quality requirements as per client satisfaction metrics, with active guidance from the manager
2.Responsible to develop and review content for MedInfo documents and other scientific communication deliverables as per the timelines assigned
3.Should be able to perform literature search on any given topic on different databases like PubMed and Embase
4.Responsible to follow 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
5.Responsible for grooming and mentoring juniors in improving writing
6.Participate in assigned training programs and work on assignments as per requirement
7.Participate in client calls as per project requirements
8. Compliance to quality, confidentiality and security:
9.Adhere and follow quality systems, processes and policies
10. Comply to training and specifications
Desired Profile:
1. Minimum4 to 6 years of experience in pharmaceutical companies - clinical research
2. Understanding of any specialty area of medicine (preferred) or an overall understanding of the medical field.
3. Strong flair and passion for writing.
4. Strong written and verbal communication/presentation skills.
5. Passion for networking.
6. Being up-to-date with the latest technical/scientific developments and relating them to various projects.
Education Qualification
M. Pharm/ Pharm. D/ BDS / MDS/Ph.D./ Any life science graduate See Less
Additional Information
Cab Facility ProvidedAbout Company
Indegene helps global healthcare organizations address complex challenges by seamlessly integrating analytics, technology, operations and medical expertise. Indegene helps clients drive outcomes, revenue and productivity improvements by making giant leaps in digital transformation, customer engagement, health reform, healthcare cost reduction, and health outcomes improvement.
Indegene has a global footprint with offices in North America, Europe, China and India.
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