Job details
Job title: Senior Medical Information Writer
- Hiring Manager: Head Scientific Communications
- Location : Hyderaba d
- % of travel expected : Travel required as per business need
- Job type: Permanent and Full time
Sanofi Global Hub is an internal Sanofi resource organization based in India and is set up to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, R&D, Data & Digital functions. Sanofi Global Hub strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, globally . Main responsibilities:
Responsible for research and authoring of scientific response documents under the direction of the Global Medical Information (GMI) team in support of global and local medical information activities. Responsible for the execution of activities as required in alignment with GMI colleagues . Achieved through a combination of product knowledge, along with editing, writing, and document management proficiency . Essential Job duties and responsibilities: 1) Conducts literature searches and reviews, and extracts/summarizes complex data from the scientific literature . 2) Generates evidence-based, accurate , current, and fair-balanced summaries of data for the creation/maintenance of scientific response documents for products in designated therapeutic area(s) . 3) Adapts global scientific response documents for assigned countries . 4) Develops responses to escalated inquiries for assigned countries . 5) Develops contributions to US NDA Annual Reports . 6) Contributes to US compendia reviews . 7) Contributes to peer reviews . 8) Demonstrates resolve and urgency to accomplish tasks without direct authority or control. Participate in cross-functional project teams as needed . Ensure that assigned projects are completed on schedule. 9) Develops and maintains Therapeutic Area expertise . 10) Reviews the content created by peer writers . 11) Collaborates effectively with Global Medical Information teams to execute content plans
- People: 1) Maintain effective relationships with the end stakeholders (Medical scientific community) within the allocated Global business unit and product – with an end objective to develop medical information content as per requirement. 2) Interact effectively with stakeholders in medical and pharmacovigilance departments. 3) Constantly assist other medical information writers in developing knowledge and sharing expertise .
- Performance: Provide deliverables (scientific response documents, US NDA Annual Reports, US compendia reviews) as per agreed timelines and quality
- Process: 1) Act as an expert in the field of medical information writing and maintain on the regulatory requirement for countries supported. 2) Assist the assigned medical information team in conducting a comprehensive medical writing needs analysis. 3) Implement relevant elements of content plans and associated activities for the year identified for the assigned countries. 4) Work with selected vendors within the region to deliver the required deliverables as per the defined process . 5) Design an overall plan of action basis end-customers feedback & improve course content and delivery .
- Stakeholders: 1) Work closely with medical teams in regions/areas to identify medical writing needs and assist in developing assigned deliverables. 2) Liaise with the Medical department to prepare relevant & customized deliverables.
- Experience: >5 years of experience in medical writing for the pharmaceuticals/ healthcare industry or equivalent experience in a clinical setting; At least 2-3 years of direct medical information experience in a pharmaceutical company
- Soft skills: Stakeholder management; communication skills; and ability to work independently and within a team environment
- Technical skills: As applicable (Including but not limited to Medical operational excellence, time, and risk management skills, Excellent technical ( medical ) editing and writing skills , Knowledge about literature evaluation and multilevel response development )
- Education: Advanced degree in life sciences/ pharmacy/ similar discipline, or medical degree or doctorate degree (PharmD, Ph.D , Master in science , MBA or equivalent)
- Languages: Excellent knowledge of the English language (spoken and written)
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'42000232', 'contact_id' => '3773199', 'recruiter_id' => '74726', 'job_function_id' => null, 'title' => 'Senior Medical Information Writer', 'vacancies' => null, 'job_type_id' => null, 'description' => null, 'pay_status' => 'Free', 'external_job_description' => '<p> Job title: <i> Senior Medical Information Writer </i><ul><li><i><br> Hiring Manager: Head Scientific Communications </i></li><li><i> Location </i><i> : </i><i> Hyderaba </i><i> d </i></li><li><i> % of travel expected </i><i> : Travel </i><i> required </i><i> as per business need </i></li><li><i> Job type: Permanent </i><i> and </i><i> Full time </i></li></ul><i><br> About the job </i><br> Our Team: <i> Sanofi Global Hub is an internal Sanofi resource organization based in India and is </i><i> set up </i><i> to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, R&D, Data & Digital functions. Sanofi Global Hub strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, globally </i><i> . </i><br> Main responsibilities: <i> Responsible for research and authoring of scientific response documents under the direction of </i><i> the </i><i> Global Medical Information (GMI) team in support of global and local medical information activities. </i><i> Responsible for </i><i> the </i><i> execution of activities as </i><i> required </i><i> in alignment with GMI colleagues </i><i> . </i><i> Achieved through a combination of product knowledge, along with editing, writing, </i><i> and </i><i> document management </i><i> proficiency </i><i> . </i><i><br> Essential Job duties and responsibilities: 1)</i> <i> Conducts literature searches and reviews, </i><i> and </i><i> extracts/summarizes complex data from </i><i> the </i><i> scientific literature </i><i> . 2) </i><i> Generates evidence-based, </i><i> accurate </i><i> , current, and fair-balanced summaries of data for the creation/maintenance of scientific response documents for products in designated therapeutic area(s)</i><i> . 3)</i><i> Adapts global scientific response documents for assigned countries </i><i> . 4) </i><i> Develops responses to escalated inquiries for assigned countries </i><i> . 5) </i><i> Develops contributions to US NDA Annual Reports </i><i> . 6) </i><i> Contributes to US compendia reviews </i><i> . 7) </i><i> Contributes to peer reviews </i><i> . 8) </i><i> Demonstrates resolve and urgency to </i><i> accomplish </i><i> tasks without direct authority or control. Participate in cross-functional project teams as needed </i><i> . </i><i> Ensure that assigned projects are completed on schedule. </i><i> 9) </i><i> Develops and </i><i> maintains </i><i> Therapeutic Area </i><i> expertise </i><i> . 10) </i><i> Reviews the content created by peer writers </i><i> . 11) </i><i> Collaborates effectively with Global Medical Information teams to execute content plans </i><ul><li><i><br> People: 1)</i><i> Maintain effective relationships with the end stakeholders (Medical scientific community) within the </i><i> allocated </i><i> Global business unit and product – with an end </i><i> objective </i><i> to develop medical information content as per requirement. 2) Interact effectively with stakeholders in medical and pharmacovigilance departments. 3) Constantly </i><i> assist </i><i> other medical information writers in developing knowledge and sharing </i><i> expertise </i><i> . </i></li><li><i> Performance: </i><i> Provide deliverables (scientific response documents, US NDA Annual Reports, US compendia reviews) as per agreed timelines and quality </i></li><li><i> Process: </i><i>1)</i><i> Act as an expert in the field of medical information writing and </i><i> maintain </i><i> on the regulatory requirement for countries supported. 2) Assist the assigned medical information team in conducting a comprehensive medical </i><i> writing needs </i><i> analysis. 3) Implement relevant elements of content plans and associated activities for the year </i><i> identified </i><i> for the assigned countries. </i><i>4) </i><i> Work with selected vendors within the region to deliver the required deliverables as per the defined process </i><i> . 5) </i><i> Design an overall plan of action basis end-customers feedback & improve course content and delivery </i><i> . </i></li><li><i> Stakeholders: </i><i> 1) </i><i> Work closely with medical teams in regions/areas to </i><i> identify </i><i> medical writing needs and </i><i> assist </i><i> in developing assigned deliverables. 2) Liaise with the Medical department to prepare relevant & customized deliverables. </i></li></ul><i><br> About you </i><ul><li><br> Experience: <i>>5 years of experience in medical writing for the pharmaceuticals/ healthcare industry or equivalent experience in a clinical setting; </i><i> At least 2-3 years of direct medical information experience in a pharmaceutical company </i></li><li>Soft skills: <i> Stakeholder management; communication skills; and ability to work independently and within a team environment </i></li><li>Technical skills: <i> As applicable (Including but not limited to </i> <i> Medical operational excellence, time, and risk management skills, </i><i> Excellent technical (</i><i> medical </i><i>) editing and writing skills </i><i> , </i><i> Knowledge about literature evaluation and multilevel response development </i><i>)</i></li><li>Education: <i> Advanced degree in life sciences/ pharmacy/ similar discipline, or medical degree or doctorate degree (PharmD, </i><i> Ph.D </i><i> , </i><i> Master in science </i><i> , MBA or equivalent)</i></li><li>Languages: <i> Excellent knowledge of the English language (spoken and written)</i></li></ul>At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. 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Office Admin Skills is an in-depth training course, you will develop the most in-demand skills to kickstart your career, as well as upgrade your existing knowledge & skills.<br /> <br /> The training materials of the Office Admin Skills course are available online for you to learn at your own pace and fast-track your career with ease.<br /> <br /> <strong>Key Features of the Office Admin and Organisation Skills Course</strong><br /> <br /> Our trusted, high-quality and affordable Office Admin and Organisation Skills course trains individuals to become experts in their field. <ul> <li>Accredited by CPD</li> <li>Instant e-certificate and hard copy dispatch by next working day</li> <li>Fully online, interactive course with audio voiceover</li> <li>Developed by qualified professionals in the field</li> <li>Discounts on bulk purchases</li> <li>Self-paced learning and laptop, tablet, smartphone-friendly</li> <li>24/7 Learning Assistance</li> </ul> <strong>Who should take the course?</strong><br /> <br /> Anyone with a knack for learning new skills can take this <strong>Office Admin Skills</strong> course. 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And a good understanding of the English language, numeracy, and ICT will be helpful.', 'school' => 'John Academy', 'keywords' => 'Medical Office Procedures,Medical Billing and Coding,Healthcare Terminology,Health Law and Ethics,Medical Documentation', 'location' => 'Online', 'duration' => 'Upto 3 Hours', 'timing' => 'Flexible', 'cost' => null, 'discount' => null, 'eligibility_criteria' => null, 'job_matching_keywords' => null, 'boosted' => '0', 'lang_code' => 'en', 'status' => 'active', 'auto_translated' => '0', 'objectives' => null, 'photo' => null, 'photo_cta' => null, 'video' => null ), 'Profile' => array() ) ) $job = array( 'Job' => array( 'id' => '42000232', 'contact_id' => '3773199', 'recruiter_id' => '74726', 'job_function_id' => null, 'title' => 'Senior Medical Information Writer', 'vacancies' => null, 'job_type_id' => null, 'description' => null, 'pay_status' => 'Free', 'external_job_description' => '<p> Job title: <i> Senior Medical Information Writer </i><ul><li><i><br> Hiring Manager: Head Scientific Communications </i></li><li><i> Location </i><i> : </i><i> Hyderaba </i><i> d </i></li><li><i> % of travel expected </i><i> : Travel </i><i> required </i><i> as per business need </i></li><li><i> Job type: Permanent </i><i> and </i><i> Full time </i></li></ul><i><br> About the job </i><br> Our Team: <i> Sanofi Global Hub is an internal Sanofi resource organization based in India and is </i><i> set up </i><i> to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, R&D, Data & Digital functions. Sanofi Global Hub strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, globally </i><i> . </i><br> Main responsibilities: <i> Responsible for research and authoring of scientific response documents under the direction of </i><i> the </i><i> Global Medical Information (GMI) team in support of global and local medical information activities. </i><i> Responsible for </i><i> the </i><i> execution of activities as </i><i> required </i><i> in alignment with GMI colleagues </i><i> . </i><i> Achieved through a combination of product knowledge, along with editing, writing, </i><i> and </i><i> document management </i><i> proficiency </i><i> . </i><i><br> Essential Job duties and responsibilities: 1)</i> <i> Conducts literature searches and reviews, </i><i> and </i><i> extracts/summarizes complex data from </i><i> the </i><i> scientific literature </i><i> . 2) </i><i> Generates evidence-based, </i><i> accurate </i><i> , current, and fair-balanced summaries of data for the creation/maintenance of scientific response documents for products in designated therapeutic area(s)</i><i> . 3)</i><i> Adapts global scientific response documents for assigned countries </i><i> . 4) </i><i> Develops responses to escalated inquiries for assigned countries </i><i> . 5) </i><i> Develops contributions to US NDA Annual Reports </i><i> . 6) </i><i> Contributes to US compendia reviews </i><i> . 7) </i><i> Contributes to peer reviews </i><i> . 8) </i><i> Demonstrates resolve and urgency to </i><i> accomplish </i><i> tasks without direct authority or control. Participate in cross-functional project teams as needed </i><i> . </i><i> Ensure that assigned projects are completed on schedule. </i><i> 9) </i><i> Develops and </i><i> maintains </i><i> Therapeutic Area </i><i> expertise </i><i> . 10) </i><i> Reviews the content created by peer writers </i><i> . 11) </i><i> Collaborates effectively with Global Medical Information teams to execute content plans </i><ul><li><i><br> People: 1)</i><i> Maintain effective relationships with the end stakeholders (Medical scientific community) within the </i><i> allocated </i><i> Global business unit and product – with an end </i><i> objective </i><i> to develop medical information content as per requirement. 2) Interact effectively with stakeholders in medical and pharmacovigilance departments. 3) Constantly </i><i> assist </i><i> other medical information writers in developing knowledge and sharing </i><i> expertise </i><i> . </i></li><li><i> Performance: </i><i> Provide deliverables (scientific response documents, US NDA Annual Reports, US compendia reviews) as per agreed timelines and quality </i></li><li><i> Process: </i><i>1)</i><i> Act as an expert in the field of medical information writing and </i><i> maintain </i><i> on the regulatory requirement for countries supported. 2) Assist the assigned medical information team in conducting a comprehensive medical </i><i> writing needs </i><i> analysis. 3) Implement relevant elements of content plans and associated activities for the year </i><i> identified </i><i> for the assigned countries. </i><i>4) </i><i> Work with selected vendors within the region to deliver the required deliverables as per the defined process </i><i> . 5) </i><i> Design an overall plan of action basis end-customers feedback & improve course content and delivery </i><i> . </i></li><li><i> Stakeholders: </i><i> 1) </i><i> Work closely with medical teams in regions/areas to </i><i> identify </i><i> medical writing needs and </i><i> assist </i><i> in developing assigned deliverables. 2) Liaise with the Medical department to prepare relevant & customized deliverables. </i></li></ul><i><br> About you </i><ul><li><br> Experience: <i>>5 years of experience in medical writing for the pharmaceuticals/ healthcare industry or equivalent experience in a clinical setting; </i><i> At least 2-3 years of direct medical information experience in a pharmaceutical company </i></li><li>Soft skills: <i> Stakeholder management; communication skills; and ability to work independently and within a team environment </i></li><li>Technical skills: <i> As applicable (Including but not limited to </i> <i> Medical operational excellence, time, and risk management skills, </i><i> Excellent technical (</i><i> medical </i><i>) editing and writing skills </i><i> , </i><i> Knowledge about literature evaluation and multilevel response development </i><i>)</i></li><li>Education: <i> Advanced degree in life sciences/ pharmacy/ similar discipline, or medical degree or doctorate degree (PharmD, </i><i> Ph.D </i><i> , </i><i> Master in science </i><i> , MBA or equivalent)</i></li><li>Languages: <i> Excellent knowledge of the English language (spoken and written)</i></li></ul>At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. 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Hiring company
Sanofi
Sanofi multinational pharmaciieutical company in Egypt
Ibd3a Academy in Egypt
Brooklen Academy
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