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medical officer

Emmes Group

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 Bengaluru, India
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 Medical &amp; Safety
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 Yes
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 Regular Full-Time
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 2748
 
 
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 Emmes Global
 
 
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 Get future jobs matching this search
 
 
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 Overview
 
 
 
 Job Description
 
 
 
 Job Posting Title
 
 
 
 
 India Bengaluru - hybrid
 
 
 
 Emmes Group: Building a better future for us all.
 
 
 Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience.
 
 
 We believe the work we do will have a direct impact on patients&rsquo; lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We&rsquo;re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us!
 
 
 
 Primary Purpose
 
 
 
 The Medical Officer has functional responsibility for medical monitoring of clinical trials, medical reviewing of activities and for broad spectrum of internal and external medical consulting, including, but not limited to, advising related to protocol development, preparation of medical strategy for feasibility studies, involvement in bid preparation and bid defense meetings, delivery of medical trainings for relevant stakeholders, professional engagement with external clinical experts, etc.
 
 
 
 Responsibilities
 
 
 
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 Works directly with the Head of Pharmacovigilance and Medical Monitoring, in managing both corporate and project-related activities. Cooperates directly with Safety Monitors, Project Leadership, Data Managers and other relevant functional groups.
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 At the project level, will function in the role of a Medical Monitor leading the clinical trial monitoring of safety and efficacy data for the assigned protocols in scope of the contract with the client and in compliance with relevant SOP and/or other relevant study specific documents.
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 Provides safety oversight throughout the lifecycle of the clinical study including evaluation, assessment, and monitoring of safety events and protocol deviations.
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 Cooperates with Safety Monitors to implement safety management activities and achieve study project objectives.
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 Evaluates adverse events, serious adverse events (SAE) including expedited reporting, as well as other protocol defined safety events.
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 Reviews SAE narratives and other safety reports.
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 Reviews IND/IDE safety reports (MedWatch safety reports, FDA Form 3500A), Council for International Organizations of Medical Sciences (CIOMS) safety reports, Development Safety Update Reports (DSUR), and other aggregate reports as applicable.
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 Reviews and approves Medical Dictionary for Regulatory Activities (MedDRA) and WHO Drug coding.
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 Reviews the FDA MedWatch Alerts, safety communications and/or other communications from other relevant Regulatory Authorities and recommends action for implementation by study teams, as applicable.
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 Provides medical input during development of protocol and associated documents &ndash; in scope agreed with the client, primarily focusing on the safety aspect of the clinical development.
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 Advises study sponsor and study team on protocol development, inclusion/exclusion criteria, eligibility questions, protocol study design and halting rules, etc.
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 Per agreement with client ensures the medical and scientific quality of safety sections of documents such as clinical trial protocols, investigator&rsquo;s brochure, informed consent document, patient diaries, and case report forms.
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 Works directly with project-level staff to develop appropriate study documents and project plans (e.g., Safety Monitoring Plan, Medical Monitoring Plan, Communication Plan, and Training Plan).
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 Supports preparation of safety section of clinical trial reports such as annual reports and clinical study reports.
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 Engages with safety oversight committees (SOC) and consults with sponsors, investigators, and pharmaceutical partners, as appropriate.
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 Participates in safety oversight committee meetings (DSMB/DMC/SMC); answers questions about safety monitoring and related procedures (e.g., review of halting rules).
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 Reviews SOC Charter, safety reports, and meeting minutes.
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 Participates in sponsor meetings and investigator training meetings.
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 Participates in regulatory (FDA or other) meetings and scientific review meetings.
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 Interacts with pharmaceutical companies and other study partners.
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 Cooperates with business development teams as medical expert, participates in bid preparation and bid presentations.
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 Acts as the internal medical consultant in broad spectrum of activities, e.g., prepares medical strategy for the feasibility activities and proposal of country mix, ensures relevant medical training for the assigned project staff, engages with identified external consultants to gain information from clinical practice, etc.
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 If contracted with client and if relevant to level of own medical expertise, Medical Officer provides broad spectrum of medical consultancy services, including medical review of relevant documents and/or data (e.g., clinical study specific documents, clinical study report, training materials, scientific communication or communication materials with medical content, etc.).
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 Participates in corporate process improvement and corporate quality assurance activities through Internal Quality Audit Team (IQAT) processes, SOP development, participation in internal and external audits, and professional development activities.
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 Other corporate activities include annual SOP reviews, participation in corporate safety meetings/activities, and other relevant corporate activities.
 
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 Qualifications
 
 
 
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 Medical Doctor (MD, MBBS, MBBCh, or other equivalent) degree is required.
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 2 years of working experience, preferably a combination of clinical practice and experience in the area of pharmaceutical medicine (i.e., clinical research, pharmacovigilance, medical affairs, regulatory etc.).
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 Demonstrated clinical medicine expertise through practice experience preferred.
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 Excellent clinical judgement and ability to communicate complex clinical issues in a scientifically sound and understandable way.
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 Experience working with regulatory submissions.
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 Expertise in safety and/or medical monitoring and serious adverse event reporting preferred.
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 Demonstrated experience with or training in clinical trial data collection.
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 Ability to work as a team member and function on a cross-functional team.
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 Ability to direct activities and encourage positive team-based culture.
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 Capacity to provide leadership and creativity in the work environment.
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 Excellent verbal and written communication skills.
 
 
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 CONNECT WITH US!
 
 
 
 
 Follow us on Twitter - @EmmesCRO
 
 
 
 
 Find us on LinkedIn - Emmes
 
 
 
</div>

Medical Officer

VSH Hospital

<div>
 Medical Services 5 Years of Experience Salary: ₹1000000.00 LPA Qualification: MD Posted on December 27, 2025
 
 
 
 Job Summary
 
 
 
 A radiologist's job involves using medical imaging (X-ray, CT, MRI, Ultrasound) to diagnose and treat diseases, requiring analysis of scans, writing detailed reports for other doctors, and communicating findings, sometimes performing image-guided procedures like biopsies, ensuring patient safety, and staying updated on technology. They're medical doctors who interpret visual data to identify issues like fractures, tumors, or heart conditions, guiding patient care plans
 
 
 Interested can share resume to
 
 hr@vshhospital.com or whats app 7022660333
 
 
 
 
 Responsibilities
 
 
 
 Key Responsibilities
 
 
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 Interpret Medical Images: Analyze various imaging modalities (X-rays, CT, MRI, ultrasound) to diagnose and monitor diseases.
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 Collaborate with Healthcare Professionals: Work closely with referring physicians and other medical staff to discuss findings and determine appropriate treatment plans.
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 Perform Interventional Procedures: Conduct image-guided procedures such as biopsies, drainages, and injections when necessary.
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 Ensure Patient Safety: Follow radiation safety protocols and ensure that imaging equipment is functioning correctly to protect patients and staff.
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 Maintain Accurate Records: Document findings and maintain patient records in compliance with healthcare regulations.
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 Stay Updated: Keep abreast of advancements in radiology and imaging technology to provide the best patient care possible.
 
 
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 </ul>
 Skill Required
 
 
 
 Required Skills And Qualifications
 
 
 
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 Medical Degree: Must have a Doctor of Medicine (MD) or Doctor of Osteopathic Medicine (DO) degree, with specialized training in radiology.
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 Licensure: Must be licensed to practice medicine in the relevant jurisdiction and board-certified in radiology.
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 Analytical Skills: Strong ability to interpret complex medical images and make accurate diagnoses.
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 Communication Skills: Excellent verbal and written communication skills to convey findings to patients and healthcare teams effectively.
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 Attention to Detail: High level of precision in analyzing images and documenting results.
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 </ul>
</div>

Radiologist Doctor

2070 Health

<div>
 
 
 About The Company
 
 
 
 
 Elevate Now is India's first medical weight-loss company, transforming how people approach weight management through science-based, doctor-led programs. We combine modern medical interventions, personalized nutrition, and dedicated health coaching to deliver sustainable results &mdash; not just short-term weight loss. Our mission is to help individuals improve their health, confidence, and long-term well-being through evidence-based, compassionate care.
 
 
 
 
 About The Role
 
 
 
 
 We are looking for a clinically strong, research-driven leader to design all medical protocols, frameworks, and doctor-facing systems. This role is ideal for someone deeply scientific, detail-oriented, and experienced in obesity care, GLP, and evidence-based clinical operations.
 
 
 
 
 Requirements
 
 
 
 
 
 Key Responsibilities
 
 
 
 
 Clinical Strategy, Training &amp; Protocol Design
 
 
 
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 Design, standardise, and optimise treatment protocols, clinical workflows, and patient care journeys
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 Build structured doctor training content, onboarding modules, and upskilling frameworks
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 Ensure all protocols follow ethical guidelines, GLP principles, and regulatory standards
 
 
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 Doctor Network Leadership
 
 
 
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 Lead doctor hiring strategy, competency framework, and selection standards
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 Build and nurture a strong network of in-house and consultant doctors
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 Mentor, coach, and support doctors on clinical quality and patient management
 
 
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 Quality, Compliance &amp; Collaboration
 
 
 
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 Oversee clinical governance, medical accuracy, and quality benchmarks
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 Work cross-functionally with product, tech, ops, and leadership to integrate clinical excellence
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 Track patient outcomes, treatment efficacy, and feedback to refine protocols
 
 
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 </ul>
 
 
 Requirements
 
 
 
 
 <ul>
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 MBBS required (MD preferred)
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 Strong knowledge of obesity medicine, nutrition, weight management, and supplements
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 6-10 years in clinical operations, medical advisory, or digital health
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 Strong scientific temperament, analytical mindset, excellent communication
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 Bangalore-based, comfortable in a fast-paced hybrid startup culture
 
 
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 Benefits
 
 
 
 
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 Top Benefit: You work with Super-Smart people
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 Industry competitive salary
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</div>

AD - Doctor Operations & Clinical Protocols (MBBS)

Accenture in India

<div>
 
 Skill required:
 
 Claims Appeals - Claims Administration
 
 
 
 Designation:
 
 Health Admin Services Associate
 
 
 
 Qualifications:
 
 Any Graduation
 
 
 
 Years of Experience:
 
 1 to 3 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&mdash; all powered by the world&rsquo;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?
 
 Embedding digital transformation in healthcare operations end-to-end, driving superior outcomes and value realization today, and enabling streamlined operations to serve the emerging health care market of tomorrow Claims Appeals involves reviewing and processing appeals for denied insurance claims. This includes evaluating the reasons for denial, gathering additional information, and making decisions on the appeal. The goal is to ensure fair and accurate resolution of claims. Responsibilities include communicating with claimants, analyzing documentation, and adhering to regulatory guidelines. This role is essential for maintaining trust and satisfaction in the claims process. Includes the administration of health, life, and property &amp; causality claims. Includes activities involved in core claim processing such as registering claims, editing &amp; verification, claims evaluation, and examination &amp; litigation.
 
 
 
 What are we looking for?
 
 
 
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 Conduct pre-service and retrospective Provider and Member Appeals for outpatient and inpatient requests. Reviews service requests to ensure compliance with applicable criteria, medical policy, and member eligibility, benefits, and contracts.
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 Utilize client specific criteria sets (e.g., Milliman or InterQual), applicable client specific medical policy and client clinical guidelines for decision making to either approve, request for additional clinical information or summarize and route to Client s nursing reviewer and/or Client s medical staff for review.
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 Accurately routes cases to client medical staff for further review when a service or admission does not meet medical necessity, place of service, or benefit criteria.
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 Responsible for conducting medical management review activities which require the review of clinical information against client specific criteria as noted above but excludes denial determinations.
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 Ensure member access to medically necessary, quality healthcare in a cost-effective setting according to contract. Consult with clinical reviewers and/or U.S.-licensed medical directors to ensure medically appropriate, high-quality, cost-effective care throughout the medical management process.
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 Graduate of any college degree or High School Diploma with 6 months&rsquo; BPO work experience.
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 At minimum 6 months of work experience.
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 Excellent written and verbal communication skills in English
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 Must pass American English and alternate language fluency test (&ldquo;Test&rdquo;) upon hire (non-US resident). For voice accounts, must pass US Berlitz B2 level or Versant score of 58 or any language proficiency equivalence.
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 Proficiency in basic computer knowledge with the ability to learn additional computer programs.
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 Holds current and unrestricted local Registered Nurse license.
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 Bachelor of Science Nursing (BSN) degree or General Nursing &amp; Midwifery (GNM) Diploma or Basic Bachelor of Science (BSC) in Nursing degree or Associate Nursing Degree or Nursing Diploma
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 A minimum of three (3) months of prior working experience as a Registered Nurse in a clinical setting required.
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 Three months is equivalent to 480 hours of working experience as an RN Roles and Responsibilities:
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 In this role you are required to solve routine problems, largely through precedent and referral to general guidelines
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 Your expected interactions are within your own team and direct supervisor
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 You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments
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 The decisions that you make would impact your own work
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 You will be an individual contributor as a part of a team, with a predetermined, focused scope of work
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 Please note that this role may require you to work in rotational shifts, Any Graduation
 
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 </ul>
</div>

Health Admin Services Associate-Voice

<div>
 
 Skill required:
 
 Claims Appeals - Claims Administration
 
 
 
 Designation:
 
 Health Admin Services Senior Analyst
 
 
 
 Qualifications:
 
 Any Graduation
 
 
 
 Years of Experience:
 
 5 to 8 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&mdash; all powered by the world&rsquo;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?
 
 Embedding digital transformation in healthcare operations end-to-end, driving superior outcomes and value realization today, and enabling streamlined operations to serve the emerging health care market of tomorrow Claims Appeals involves reviewing and processing appeals for denied insurance claims. This includes evaluating the reasons for denial, gathering additional information, and making decisions on the appeal. The goal is to ensure fair and accurate resolution of claims. Responsibilities include communicating with claimants, analyzing documentation, and adhering to regulatory guidelines. This role is essential for maintaining trust and satisfaction in the claims process. Includes the administration of health, life, and property &amp; causality claims. Includes activities involved in core claim processing such as registering claims, editing &amp; verification, claims evaluation, and examination &amp; litigation.
 
 
 
 What are we looking for?
 
 
 
 <ul>
 <li>
 Conduct pre-service and retrospective Provider and Member Appeals for outpatient and inpatient requests. Reviews service requests to ensure compliance with applicable criteria, medical policy, and member eligibility, benefits, and contracts.
 </li>
 <li>
 Utilize client specific criteria sets (e.g., Milliman or InterQual), applicable client specific medical policy and client clinical guidelines for decision making to either approve, request for additional clinical information or summarize and route to Client s nursing reviewer and/or Client s medical staff for review.
 </li>
 <li>
 Accurately routes cases to client medical staff for further review when a service or admission does not meet medical necessity, place of service, or benefit criteria.
 </li>
 <li>
 Responsible for conducting medical management review activities which require the review of clinical information against client specific criteria as noted above but excludes denial determinations.
 </li>
 <li>
 Ensure member access to medically necessary, quality healthcare in a cost-effective setting according to contract. Consult with clinical reviewers and/or U.S.-licensed medical directors to ensure medically appropriate, high-quality, cost-effective care throughout the medical management process.
 </li>
 <li>
 Graduate of any college degree
 </li>
 <li>
 At minimum 3 year experience or related Accenture or other outsourcing experience or returning CL12 or CL11 employee (including meeting or exceeding currently published quality and productivity standards and have passed the promotion eligibility and certification requirements).
 </li>
 <li>
 Excellent written and verbal communication skills in English.
 </li>
 <li>
 Must pass American English and alternate language fluency test (&ldquo;Test&rdquo;) upon hire (non-US resident). For voice accounts, must pass US Berlitz B2 level or Versant score of 58 or any language proficiency equivalence.
 </li>
 <li>
 Proficiency in basic computer knowledge with the ability to learn additional computer programs.
 </li>
 <li>
 Maintains active USRN Licensure.
 </li>
 <li>
 Responsible for notifying Team Lead, Manager, and/or Compliance Department immediately of any expiration or change in status of active USRN licensure. Does not perform clinical duties unless active licensure is documented and on file within the PMO department.
 </li>
 <li>
 Adheres to production and quality metrics.
 </li>
 <li>
 Holds current and unrestricted local Registered Nurse license.
 </li>
 <li>
 Bachelor of Science Nursing (BSN) degree or General Nursing &amp; Midwifery (GNM) Diploma or Basic Bachelor of Science (BSC) in Nursing degree or Diploma Roles and Responsibilities:
 </li>
 <li>
 In this role you are required to do analysis and solving of increasingly complex problems
 </li>
 <li>
 Your day to day interactions are with peers within Accenture
 </li>
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 You are likely to have some interaction with clients and/or Accenture management
 </li>
 <li>
 You will be given minimal instruction on daily work/tasks and a moderate level of instruction on new assignments
 </li>
 <li>
 Decisions that are made by you impact your own work and may impact the work of others
 </li>
 <li>
 In this role you would be an individual contributor and/or oversee a small work effort and/or team
 </li>
 <li>
 Please note that this role may require you to work in rotational shifts, Any Graduation
 
 </li>
 </ul>
</div>

Health Admin Services Senior Analyst-Voice

Apollo Hospitals

<div>
 
 Qualification
 
 
 
 
 Job Purpose
 
 
 
 Graduate; 1st division in 10th, 12th and
 
 GNM Nursing/BSc Nursing/M.Sc Nursing
 
 
 
 
 Relevant Experience
 
 
 
 3 months 5 years of experience in the field of Nursing assessing patients health problems, providing care to sick, disabled, recovering or injured patients, maintaining important medical records, implementing a nursing care plan and advising patients about maintaining health.
 
 
 
 Responsibilities
 
 
 
 <ul>
 <li>
 Recording medical history and symptoms
 </li>
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 Administering medication and treatment
 </li>
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 Collaborating with teams for patient care
 </li>
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 Performing point of care tests
 </li>
 <li>
 Conducting nursing assessment
 </li>
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 Monitoring patients health
 </li>
 <li>
 Providing support and education to patient and family
 </li>
 <li>
 Maintaining inventory
 </li>
 <li>
 Providing bedside care
 </li>
 <li>
 Operating and care of medical equipment
 </li>
 <li>
 Attending regular in-service education
 
 
 </li>
 </ul>
 
 Requirements And Skills
 
 
 
 <ul>
 <li>
 Interpersonal relationship skills
 </li>
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 Listening
 </li>
 <li>
 Team building
 </li>
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 Perceptual
 </li>
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 Communication
 </li>
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 Coordination and cooperation
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 Initiative
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 <li>
 Moral support and physical approach to patient
 </li>
 <li>
 Computer literacy
 </li>
 <li>
 GNM Nursing/BSc Nursing/M.Sc Nursing
 
 
 </li>
 </ul>
 Dear Candidate,
 
 
 We are delighted to introduce you to Apollo Hospitals, a leading healthcare provider in India. With a long-standing heritage spanning many decades, Apollo Hospitals has established itself as a trusted name in the healthcare field, consistently delivering exceptional care with compassion.
 
 
 Renowned for our state-of-the-art medical facilities, advanced technology, and a highly skilled and dedicated team of healthcare professionals, Apollo Hospitals is committed to providing quality care and ensuring patient satisfaction in everything we do.
 
 
 Our organization strives to offer comprehensive healthcare services across various specialties and disciplines. From primary care to specialized treatments, we provide a wide range of medical services to cater to the diverse needs of our patients. Our hospital is equipped with cutting-edge technology, modern infrastructure, and an experienced team of doctors, nurses, and support staff who collaborate to deliver the highest standards of healthcare.
 
 
 At Apollo Hospitals, we believe in fostering continuous learning and innovation. We prioritize research and development to remain at the forefront of medical advancements, enabling us to provide the latest treatments and therapies to our patients. We also emphasize preventive care and wellness programs, promoting a healthy lifestyle and helping individuals maintain optimal health.
 
 
 Furthermore, Apollo Hospitals holds a strong commitment to social responsibility. Through various initiatives, we strive to make quality healthcare accessible to all members of society, regardless of their socio-economic background. We actively participate in community health programs, awareness campaigns, and outreach activities to promote healthcare education and support underserved populations.
 
 
 As you join our team, we invite you to embody the values and culture of Apollo Hospitals. Our core principles include prioritizing patient-centric care, fostering teamwork, upholding integrity, and embracing compassion in all that we do. Together, we have the power to make a significant impact on the lives of our patients and contribute to the progress of healthcare in our community.
 
 
 We are excited about the opportunity to collaborate with you, harnessing your skills and expertise to deliver exceptional care and service to our patients. If you have any inquiries or would like to explore more about Apollo Hospitals, please don't hesitate to contact our team.
 
 
 Thank you for joining the Apollo Hospitals family. We are thrilled to begin this journey together, striving for excellence in healthcare.
 
 
 Sincerely,
 
 
 Team HR
 
 
 
 Locations:
 
 Bangalore, Karnataka, India
</div>

Staff Nurse

Eli Lilly and Company

<div>
 At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We&rsquo;re looking for people who are determined to make life better for people around the world.
 
 
 
 Writer - GCH
 
 
 
 
 Purpose
 
 
 
 Scientific data and information are core assets of Lilly. Providing balanced, objective, and accurate information to regulators, the scientific community, health care professionals, payers, and patients in a consistent and timely fashion across the entire drug development lifecycle is fundamental to Lilly.
 
 
 
 Preferred
 
 
 
 As healthcare providers are deluged with data and are making choices in an increasingly complex and stressed health system, Lilly Medical Affairs is able to provide clear, credible answers that will set Lilly apart from its competitors. Medical Affairs&rsquo; mission is to make Lilly the preferred pharmaceutical partner in the healthcare community globally by leveraging its medical expertise to drive patient-centric answers and solutions.  Medical Affairs (MA) brings deep medical expertise to healthcare providers and payers. MA focuses on answering their questions with customized clinical and real-world evidence that can make the difference on if and how they use Lilly products. Additionally, MA brings clinical insights from customers back to the company to inform new product development and lifecycle planning. MA also supports patients with educational tools to help them manage their illness and with assistance to access our medicines for those facing tough financial situations. The MA content development team will be key in maintaining and creating content to support Medical Affairs activities such as:
 
 
 <ul>
 <li>
 Slide Updates
 </li>
 <li>
 Internal Training Slides
 </li>
 <li>
 Manuscript Slides
 </li>
 <li>
 Data Slides
 </li>
 <li>
 Newsletters/ bulletin
 </li>
 <li>
 QR Compendium
 </li>
 <li>
 Affiliate Regional Slides
 </li>
 <li>
 HCP &amp; patient education material
 </li>
 <li>
 Advisory board slides
 </li>
 <li>
 Competitive landscape slides
 </li>
 <li>
 Image sourcing, image redraws
 </li>
 <li>
 Lexicon
 </li>
 <li>
 MQAD (Medical Questions Analysis Document)
 
 
 
 </li>
 </ul>
 
 Primary Responsibilities
 
 
 
 This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. Consult with your supervision regarding your actual job responsibilities and any related duties that may be required for the position.
 
 
 
 EMS (Executive Medical Summary)
 
 
 
 Content Strategy and Execution: Document Preparation, Development and Finalization/Document Management
 
 
 <ul>
 <li>
 Effectively collect and evaluate data, information, and input from multiple sources, functions, and regions to create a cohesive content strategy for writing projects.
 </li>
 <li>
 Plan (including organizing/preparing outlines), write (including first-draft authoring), edit, review, coordinate, and complete the regulatory documents supporting clinical development/product registration.
 </li>
 <li>
 Conduct effective document initiation meeting to ensure authoring team alignment and understanding.
 </li>
 <li>
 Build scientific-based rationale that support the purpose of more complex and/or strategic documents.
 </li>
 <li>
 Ensure data are presented in a clear, complete, accurate, and concise manner.
 </li>
 <li>
 Ensure that key data, statements and conclusions are consistent across related documents, and that statements and conclusions are integrated, accurate, balanced and supported by appropriate data.
 </li>
 <li>
 Coordinate expert/scientific reviews, collate reviewer&rsquo;s comments, adjust content of document as required based on internal/external input, and prepare final version.
 </li>
 <li>
 Ensure and coordinate quality checks for accuracy.
 </li>
 <li>
 Exhibit flexibility in moving across development and preparation of multiple document types.
 </li>
 <li>
 Influence or negotiate change of timelines and content with other team members.
 </li>
 <li>
 Work with internal and external experts to develop and prepare presentations.
 </li>
 <li>
 As needed, may build and manage relationships with vendors/alliance partners.
 
 
 
 </li>
 </ul>
 Project and Stakeholder management
 
 
 <ul>
 <li>
 Lead the writing process and apply effective project management skills to ensure timely completion of high-quality regulatory documents.
 </li>
 <li>
 Build/communicate credible writing project timelines.
 </li>
 <li>
 Anticipate and mitigate risks to delivery
 </li>
 <li>
 Work with teams and stakeholders to ensure smooth and timely development of documents and escalate issues, as appropriate, to ensure document completion.
 </li>
 <li>
 Effectively communicate project status to stakeholders
 
 
 
 </li>
 </ul>
 Knowledge and Skills Development
 
 
 <ul>
 <li>
 Maintain and enhance therapeutic area knowledge including disease state and compound(s) for assigned project(s).
 </li>
 <li>
 Exhibit flexibility in moving across document types, therapeutic areas, and compounds, depending on project assignment.
 </li>
 <li>
 Maintain and enhance knowledge of regulatory guidelines and publication guidelines.
 </li>
 <li>
 Possess overarching view of compound, therapeutic area, and external environment (including competitors) with ability to participate effectively in clinical planning, submission strategy planning, customer regulatory responses, and/or current awareness literature updates and reviews.
 </li>
 <li>
 Maintain and enhance the scientific communications skills to align with the audience needs and with the changes in technology and platforms.
 
 
 
 </li>
 </ul>
 
 Knowledge Sharing
 
 
 
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 Provide coaching to others by sharing technical information, giving guidance, answering questions. 
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 Recognized for technical expertise in specific document development.
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 Network with others (including other functions and regions) to identify and share best practices.
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 Contribute to process improvements, suggesting opportunities where appropriate.
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 Provide database and other tool (e.g., document management systems) expertise.
 
 
 
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 </ul>
 
 Minimum Qualification Requirements
 
 
 
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 <li>
 Bachelor&rsquo;s degree in a scientific, health, communications, technology health related field.
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 Demonstrated experience in technical/ regulatory scientific writing.
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 Strong communication and interpersonal skills.
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 Successful completion of writing exercise (a writing exercise is required as part of the candidate evaluation process)
 
 
 
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 </ul>
 
 Other Information/Additional Preferences
 
 
 
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 <li>
 Graduate degree with formal research component or in life sciences.
 </li>
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 Demonstrated mastery of verbal and written English skills in the medical, scientific or technical writing fields.
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 Clinical pharmacology, therapeutic area, or other medical and scientific specific knowledge and experience specific to hiring area (e.g., neuroscience, oncology, cardiovascular, immunology or endocrine expertise).
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 Experience writing regulatory, clinical trial documents and/or publications
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 Experience writing deliverables for Medical Affairs communications (slide decks, patient or HCP materials, etc)
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 Experience in clinical development, clinical trial process or regulatory activities.
 </li>
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 Demonstrated project management and time management skills.
 </li>
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 Demonstrated high-level end-user computer skills (e.g., word processing, tables and graphics, spreadsheets, presentation and templates).
 
 
 
 </li>
 </ul>
 Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
 
 
 Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
 
 
 #WeAreLilly
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Writer - GCH

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