Manager Scientific Writing - Pharmacovigilance Job in Indegene

About Indegene:

At Indegene, we look to change healthcare for the better. Being an Indegene employee is not just doing a job, but it is about real contribution and outcomes. We are a global team of over 1,200 employees across 14 global locations. Our singular focus is to deliver real outcomes that are measurable, impactful, and sustainable. This has made us a recognized global leader and partner to some of the largest and most respected healthcare organizations.

Joining us means you will be part of a great company, one that joins hands to really improve patient and business outcomes using analytics, technology, operations, and medical expertise. Our people are exceptionally bright, motivated, and customer focused. Even though they are from diverse cultural and academic backgrounds, they have three things in commonthey are really passionate about healthcare, they are committed to their customers and teams, and they sincerely believe that collaboration is the key to achieving their personal and professional goals.

Job Summary:

The Manager Scientific WritingPharmacovigilance needs to lead and manage delivery of projects in terms of resourcing, quality, timeliness, efficiency, and high technical standards for deliveries made by the medical writing group, including scientific documents and clinical/medical reports. He or she contributes to overall quality enhancement by ensuring high scientific standards for the output produced by the medical writing group through expert review and feedback mechanism to the delivery teams.

Job Description:

The roles and responsibilities of the Manager Scientific WritingPharmacovigilance include the following:

Developing scientific medical content for all projects that meet international quality standards

Interfacing with clients on a regular basis to meet their expectations

Controlling/reducing the cost of content development, cycle times, and error rates in projects

Developing innovative medical content products by leveraging on the depth of scientific content

Adhering to compliance procedures and internal/operational risk controls in accordance with any and all applicable regulatory standards, requirements, and policies

Desired Skills and Experience:

EducationMD/PhD/MBBS/MPharm

Experience5-7 years of experience in pharmaceutical companies in any of the following functions: medical services/medico-marketing/clinical research/regulatory affairs; medical writing/developing/publishing medical content; or a minimum of 1-3 years of experience in any clinical practice

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 and updating oneself with the latest technical/scientific developments and relating them to various projects

Strong clinical reasoning skills

Ability to work under pressure to meet agreed deadlines

Passion, energy, and enthusiasm to drive results