Current jobs related to Medical Director - Mumbai - Ortolan Group

  • EU, Medical Director, Hematology

    3 months ago

    mumbai, India 720 GlaxoSmithKline AG Full time

    Overview Medical Affairs is a critical bridge between R&D and the commercial organization to ensure that our medicines reach the appropriate patients. GSK has committed to building a new oncology business, with initial focus on selected EU markets. To this end, this is a critical role to ensure hematology/oncology resource and activities are...

  • EU, Medical Director, Hematology

    4 months ago

    Mumbai, India 720 GlaxoSmithKline AG Full time

    Overview Medical Affairs is a critical bridge between R&D and the commercial organization to ensure that our medicines reach the appropriate patients. GSK has committed to building a new oncology business, with initial focus on selected EU markets. To this end, this is a critical role to ensure hematology/oncology resource and activities are aligned...

  • EU, Medical Director, Hematology

    1 week ago

    mumbai, India 720 GlaxoSmithKline AG Full time

    Overview Medical Affairs is a critical bridge between R&D and the commercial organization to ensure that our medicines reach the appropriate patients. GSK has committed to building a new oncology business, with initial focus on selected EU markets. To this end, this is a critical role to ensure hematology/oncology resource and activities are aligned...

  • Director - Sales - Medical Devices

    7 days ago

    Mumbai, India RGF Select India Private Limited Full time

    Director - Sales - Global leader (Medical devices) || Orthodontics We are hiring for the world-leading brand for confidence in esthetic dentistry.Position - Sales DirectorLocation - MumbaiExperience - Sales (Medical devices)Reports to : Executive Chairman - South Asia AreaDirect Reports: Zonal Sales Manager , Key Account Managers,Customer Service and...

  • Country Medical Director, India

    3 weeks ago

    Mumbai, India MSD Full time

    Job DescriptionCountry Medical Director, IndiaTHE OPPORTUNITY The Country Medical Director (CMD) is the Senior Medical Leader for Our Company in a country and serves as the leader of the medical affairs organization in their geographyBased in Mumbai, named one of the Best Companies for Women in India by Avatar, 2019.Join the premier biopharmaceutical...

  • Ayurveda Medical Officer

    5 months ago

    Mumbai, India Shri Vile Parle Kelavani Mandal Full time

    **Roles and Responsibilities**: - To provide quality of medical services and appropriate medical care in Camps conducted by Ayurveda Hospital Shirpur. - The Ayurveda Medical Officer has to handle all pre camp preparations, during the camp duty and post camp duties including data preservation, data analysis and writing of papers based on camp experiences. -...

  • Medical Billing Executive

    4 months ago

    Mumbai, India Platinum Hospitals Pvt Ltd. Full time

    **Role - Medical Records Auditor** - Eligibility Criteria - Must have a min 2 yr experience in MRD / Billing Auditing - Examining records, reports, receipts, or other documents for Admissions and Discharge - Ensure supporting documentation is available incase of any billing discounting for special cases - To develop policies and procedures relating to the...

  • Principal Medical Writer

    3 months ago

    Mumbai, Maharashtra, India Abbott Laboratories Full time

    **Primary Job Function**: - Manage the quality, accuracy, compliance with internal & external standards and the timely production of documents - Point of Contact for all medical writing/publishing activities for affiliate. - Responsible for quality and timelines of all publications. - Develop, implement and manage templates & documentation format required...

  • Medical Sales Representative

    4 months ago

    Mumbai, Maharashtra, India Continual Lifesciences Private Limited Full time

    We are hiring Medical representative (*FRESHERS ONLY) who desire to build a career in medical sales; based in Mumbai for marketing of Ayurvedic medicines and nutraceuticals. **Role**: Medical Sales Representative **Responsibilities**: Training under the directors and the team members. Attaining full knowledge about all the products manufactured and...

  • Medical Records Officer

    4 months ago

    Bandra East, Mumbai, Maharashtra, India Asian Heart Institute Full time

    **Position** An integral role focusing on managing the Medical Records Department (MRD), ensuring adherence to quality standards (ISO), and maintaining accurate medical records in compliance with ICD-10 coding. This position also involves reporting to the Medical Director, conducting medical audits, training staff, and interacting with patients, relatives,...

  • Director of Business Development

    3 weeks ago

    Mumbai, India HEALTOUR SOLUTIONS PVT LTD Full time

    **Job Title:** Director of Business Development**Company:** Healtour Solutions Pvt Ltd**Location:** HyderabadiIndustry:** Medical Tourism**Reports to:** CEO### **About Healtour Solutions:**Healtour Solutions Pvt Ltd is an award-winning medical tourism aggregator startup recognized for its excellence in medical tourism promotion. The company connects...

  • Ayurveda Medical Officer

    4 months ago

    Mumbai, India Narsee Monjee Institute of Management Studies (NMIMS) Full time

    **Roles and Responsibilities**: - To provide quality of medical services and appropriate medical care in Camps conducted by Ayurveda Hospital Shirpur. - The Ayurveda Medical Officer has to handle all pre camp preparations, during the camp duty and post camp duties including data preservation, data analysis and writing of papers based on camp experiences. -...

  • Medical Admin Opening in Hospital

    4 months ago

    Mumbai, India Eminent HR Full time

    Medical Admin Key KRAs 1. Department ALOS and discharges 2. Process Improvements 3. New Projects : process development, checklists, strategy Clinical Coordination & Floor Management 1. Floor coordination for various aspects of clinical and patient related concerns, which entails - Coordination of floor activities as and when facilitation is required. -...

  • Resident Medical Officer

    4 months ago

    Mumbai, India Surana Hospital & Research Centre Full time

    Oversee the total health program and follow all procedures. - Screen all campers as they arrive at camp, check for sickness, recent illness and prior injuries, possible abuse, or medical conditions. - Maintain an up-to-date and accurate log of all health-related incidents and procedures. - Collect all camper and staff medications, dispensing medications at...

  • Director of Business Development

    3 weeks ago

    Mumbai, India HEALTOUR SOLUTIONS PVT LTD Full time

    **Job Title:** Director of Business Development **Company:** Healtour Solutions Pvt Ltd **Location:** Hyderabad iIndustry:** Medical Tourism **Reports to:** CEO ### **About Healtour Solutions:**Healtour Solutions Pvt Ltd is an award-winning medical tourism aggregator startup recognized for its excellence in medical tourism promotion. The company connects...

  • Director of Business Development

    3 weeks ago

    Mumbai, India HEALTOUR SOLUTIONS PVT LTD Full time

    **Job Title:** Director of Business Development **Company:** Healtour Solutions Pvt Ltd **Location:** Hyderabad iIndustry:** Medical Tourism **Reports to:** CEO ### **About Healtour Solutions:**Healtour Solutions Pvt Ltd is an award-winning medical tourism aggregator startup recognized for its excellence in medical tourism promotion. The company connects...

  • Director of Business Development

    3 weeks ago

    Mumbai, India HEALTOUR SOLUTIONS PVT LTD Full time

    **Job Title:** Director of Business Development **Company:** Healtour Solutions Pvt Ltd **Location:** Hyderabad iIndustry:** Medical Tourism **Reports to:** CEO ### **About Healtour Solutions:** Healtour Solutions Pvt Ltd is an award-winning medical tourism aggregator startup recognized for its excellence in medical tourism promotion. The company...

  • Director - Medical & Scientific Affairs

    2 weeks ago

    mumbai, India Abbott Full time

    Defining internal medical leadership delivering strategic scientific direction to the organization. Responsible for the overall business support in terms of brand support to all the marketed products in India & Ex India markets– includes scientific content, content creation and approval, new product launches, competitor product profiling, sales force and...

  • Director - Medical & Scientific Affairs

    1 week ago

    mumbai, India Abbott Full time

    Defining internal medical leadership delivering strategic scientific direction to the organization. Responsible for the overall business support in terms of brand support to all the marketed products in India & Ex India markets– includes scientific content, content creation and approval, new product launches, competitor product profiling, sales force and...

  • Director - Medical & Scientific Affairs

    2 months ago

    Mumbai, India Abbott Full time

    Defining internal medical leadership delivering strategic scientific direction to the organization. Responsible for the overall business support in terms of brand support to all the marketed products in India & Ex India markets– includes scientific content, content creation and approval, new product launches, competitor product profiling, sales force and...

Medical Director

4 months ago

Mumbai, India Ortolan Group Full time

Medical Director - Regulatory Development and Strategy

Mumbai or Vadodara

Salary: Competitive + Benefits + Bonus

If you are an experienced physician / scientist with regulatory experience then we want to hear from you.

Join us to help improve peoples' lives and make healthcare better for everyone

Why Pharmanovia?

Pharmanovia is a dynamic, fast-growing international pharmaceutical company with a portfolio of over 20 brands across more than 160 markets. Our mission is to improve patient health globally through the revitalisation of niche, tried-and-trusted medicines.

Our core behaviours are:

  • We act decisively but we never compromise on quality.
  • We keep our promises and do as we say.
  • We value our heritage and foster an entrepreneurial spirit.
  • We reinvest in our future - in our products, our brands, and our people.
  • We give back to our communities.

Since its inception in 2013, Pharmanovia has grown consistently year on year, focusing on delivering high-quality branded prescription medicines to patients, prescribers, and healthcare providers across the world. Our growth has enabled the company to reinvest in its products, brands, people, and to give back to its communities. A people business with a strong, supportive culture that encourages innovation and entrepreneurial spirit, our team comprises over 300 employees and 29 nationalities, operating from offices in the UK, Denmark, Netherlands, Switzerland, U.A.E., India, Singapore, Italy, Spain, and South Korea.

We are an agile, committed, and innovative global specialty pharma business and a preferred partner for innovator pharma companies, instigating a paradigm shift in the life cycle management of iconic medicines. We seek to extensively engage with clinical communities to communicate product improvements and prioritise environmental, social, and governance considerations across the business and workforce.

Pharmanovia's therapeutic areas include Cardiovascular, Oncology, Endocrinology and Neurology.

About the role:

This is a key role which acts at the interface between the company and the regulatory authorities, through the entire life cycle of the medication, from early development, to commercialization across all our regions.

Main responsibilities:

  • Help build the regulatory strategy and plans for projects in the pipeline with focus on clinical and non-clinical aspects of the dossier.
  • Act as SME in implementing registration strategy across relevant groups, including Clinical Development, Preclinical Development, Marketing and CMC.
  • Lead and work closely with relevant clinical development, operations and research personnel to ensure regulatory compliance and consistency with regulatory registration strategy.
  • Support the build of global clinical development strategy based on correct interpretation of regulatory requirements.
  • Review and Input into clinical study protocols and reports to support the intended indications in line with regulatory requirements.
  • Authoring and reviewing the clinical sections of the dossier for regulatory submissions.
  • Manage interactions and build positive relationships with all relevant Health Authorities and service providers to facilitate timely and compliant submissions and approvals.
  • Advise senior management on regulatory and clinical strategy pathways and options for successful developments.
  • Build the orphan drug submission strategies and the scientific clinical rationales to support the strategies.
  • Provide support in post-approval clinical commitments (Registry, Phase IV Studies, RWE etc.) and digital projects with regulatory strategy for development.
  • Analyse and interpret scientific and clinical data critically to support regulatory submissions and strategies.
  • With the medical director, reviews material for communications with external stakeholders, including, promotional materials, press-releases, study ads and relevant media for regulatory compliance
  • With the quality lead ascertains the compliance of production with ICH-GCP guidelines and other relevant specifications and regulatory guidance.
  • Identification and management of external consultants.
  • Attend training lectures, symposia and conferences in order to maintain up-to-date level of knowledge and expertise.

About you:

  • Extensive experience gained in the pharmaceutical industry, ideally from within a consultancy firms, healthcare authority (MHRA, EMA or any other EU Authority) with focus on regulatory affairs and clinical Assessment and Review.
  • Experience of development in the UK, EU and RoW.
  • Up-to-date knowledge of the regulatory guidelines, a good understanding of the decision-making process in the regulatory authorities and the ability to identify trends and directions that influence the process.
  • The role requires in-depth understanding and engagement with key regulators.
  • BSc or higher academic degree (including MD, Clinical Pharmacology, Pharmacy or related scientific qualification).
  • Specific experience in late-stage development, clinical authoring and filling of MAA.
  • Experience in working with EMA, ODD, PIP, regulatory Scientific Advice Meetings and other relevant technical work EMA, FDA and other Competent Authorities.
  • Ability to analyse and interpret clinical study reports and scientific literature and deliver regulatory position papers.
  • Experience in identification and management of external consultants.
  • Up-to-date ICH-GCP certification.
  • Excellent oral and written English communication.
  • Ability to influence and negotiate effectively.
  • Ability to work well in a dynamic and constantly changing environment, with flexibility and agility.
  • Ability to work with internal and external stakeholders in a multicultural and diverse environment with respect and patience.

What we offer:

The position can be located in Mumbai or Vadodara, India or the UK/EU, and provides global coverage to the company on various development and acquisition projects. Other locations will be considered for the right applicant.

We offer a competitive salary plus bonus and rewards package including holiday, health & well-being program, employee recognition awards, social events, pension scheme and hybrid working.

By applying for this role, your details will be sent to Ortolan People, who are engaged to provide recruitment support in processing applications. We will endeavour to respond to all applicants within three working days. Occasionally for roles with a very high volume of applicants, this may not be possible.