Copywriting Analyst

Accenture; Mumbai; On-site; INR 900,000 - 1,500,000; Full time

Job summary

Accenture in Mumbai is seeking a Copywriting Analyst to develop and review medical content for clinical and regulatory documents, following regulatory guidelines. You will write high-quality scientific content and guide the team in content development for assigned modules, collaborating with medical writers and operations to ensure client expectations are met.

The role requires 3 to 5 years of experience, a graduation, and strong English skills.

Qualifications

• Graduate with 3–5 years of experience in medical writing or medical communications.
• Experience writing for medical affairs/promo medical communication and education in pharma/agency environments.
• Strong English language skills and ability to interpret clinical data and regulatory requirements.

Responsibilities

• Develop scientific content for clinical and regulatory documents following regulatory guidelines.
• Provide medical review and oversight for assigned modules/projects to ensure quality and compliance.
• Guide the team in content development using scientific expertise and client expectations.
• Collaborate with medical writers, operations, and technology teams to deliver digital content solutions.
• Participate in client pitches and business development discussions.
• Train and mentor junior writers and ensure timely delivery and audit readiness.

Skills

Marketing Operations

Medical Affairs

Education

Any Graduation

Job description

Skill required:

Marketing Operations - Medical Affairs

Designation:

Copywriting Analyst

Qualifications:

Any Graduation

Years of Experience:

3 to 5 years

About Accenture

Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song— all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. Our 784,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners and communities.Visit us at www.accenture.com

What would you do?

Able to develop content and perform medical review for various clinical and regulatory documents following regulatory guidelines.Use scientific expertise to develop high-quality medical/scientific content outlines and guide the team in content development for assigned modules/projects in line with client expectations.Experience in writing white papers, manuscripts, point of view, etc.Write scientific content for projects if the nature of the project is extremely complex and it requires expertise or based on business need.Communicate the clinical data in a clear and concise manner.Follow department best practices for processes, communication, project management, documentation, and technical requirements.Converts relevant data and information into a form that meets regional regulatory requirements.Understands and complies with appropriate conventions and other governing bodies following applicable divisional guidelines, templates, and SOPs to comply with regulatory requirements.Completes assignments independently or for more complex documents, under the guidance of a mentor.Ensure compliance with client and Accenture internal SOPs for all materials.Collaborate with technology and creative teams to develop innovative digital solutions.Participate in client pitches and business development meetings.Train and mentor scientific writers, contributing to skill development.Ensure quality delivery and client engagement for organic growth.Ability to define medical communication strategy and development of new content for brand communication.Proficiency in using Microsoft Word, Excel, PowerPoint, and Adobe Acrobat.

• Driving project execution and coordination, including planning, tracking, and ensuring timely delivery
• Supporting client communication, status reporting, and action tracking
• Collaborating cross-functionally with medical writers and operations teams
• Ensuring compliance, documentation, and audit readiness
• Adhering to established processes and identifying improvement opportunities
• Tracking and reporting key performance metrics such as timelines and task completion

What are we looking for?

ularifications and Prerequisites:Graduate (MBBS, MD or M. Pharm)8-10 Years of experience as medical writer or other relevant work experienceExperience from the pharmaceutical/life sciences industryExperience in creating medical communications content for medical affairs/promo medical communication and education, preferably within an agency or pharma environment.Experience of developing content for marketing communications channels such as Veeva approved emails, Veeva CLMs, brand/medical website, videos, etc.Strong understanding of Medical Legal Regulatory (MLR) approval process and submission of artifacts on Veeva Vault PromoMats including referencing and annotation.Have experience in writing in specialized therapy areas such as oncology, respiratory, cardiology, dermatology, vaccines, infectious diseases, nephrology, and rare diseases.Provide intellectual input across a variety of document types through literature search and analysing client assets.Experience in developing or executing medical strategic plan for a brand.Able to develop content for brands at different product lifecycle stages.Demonstrates understanding of how to interpret and document clinical data.Demonstrates knowledge of scientific methodologyExcellent English language skills (verbal and written) and strong analytical skillsStay up-to-date with the latest medical literature and industry trends to ensure that all content is relevant and reflects current scientific knowledge.Excellent attention to detail and ability to manage multiple projects simultaneously.Able to develop content and perform medical review for various clinical and regulatory documents following regulatory guidelines.Use scientific expertise to develop high-quality medical/scientific content outlines and guide the team in content development for assigned modules/projects in line with client expectations.Experience in writing white papers, manuscripts, point of view, etc.Write scientific content for projects if the nature of the project is extremely complex and it requires expertise or based on business need.Communicate the clinical data in a clear and concise manner.

Roles and Responsibilities:

n this role you are required to do analysis and solving of moderately complex problems

• May create new solutions, leveraging and, where needed, adapting existing methods and procedures
• The person would require understanding of the strategic direction set by senior management as it relates to team goals
• Primary upward interaction is with direct supervisor
• May interact with peers and/or management levels at a client and/or within Accenture
• Guidance would be provided when determining methods and procedures on new assignments
• Decisions made by you will often impact the team in which they reside
• Individual would manage small teams and/or work efforts (if in an individual contributor role) at a client or within Accenture
• Please note that this role may require you to work in rotational shifts

Any Graduation

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