Total 10 Health / Beauty / Fitness job vacancies in Hyderabad, Hyderabad

Job Summary
We are looking for an experienced Medical Advisor to provide the scientific foundation for the Therapeutic Area (TA) medical strategy, including managing various medical activities and engaging key thought leaders. Oversee the execution of the medical affairs plan, facilitate the flow of medical developments to the sales and marketing team, and contribute to the development of the Medical Affairs strategic plan for identified Therapeutic Area (TA) and products. 

Roles & Responsibilities
• You will be responsible for serving as a core scientific member of the cross-functional franchise team, providing the scientific foundation for the Therapeutic Area (TA) medical strategy.
• You will be responsible for conceptualizing and managing a wide range of medical activities, aligned with the TA Medical strategy, including research, publications, medical education, and patient support programs.
• You will be responsible for engaging key thought leaders through medical affairs activities, in line with the overall strategic plan.
• You will be responsible for ensuring the optimal execution of the strategic medical affairs plan through Regional Medical Affairs, encompassing medical education, product education, and special projects.
• You will be responsible for acting as a therapeutic area scientific expert, discussing scientific data with leading specialists, and providing training on the latest medical developments to the sales and marketing team.

Job Summary
We are looking for an experienced Medical Advisor to provide the scientific foundation for the Therapeutic Area (TA) medical strategy, including managing various medical activities and engaging key thought leaders. Oversee the execution of the medical affairs plan, facilitate the flow of medical developments to the sales and marketing team, and contribute to the development of the Medical Affairs strategic plan for identified Therapeutic Area (TA) and products. 

Roles & Responsibilities
• You will be responsible for serving as a core scientific member of the cross-functional franchise team, providing the scientific foundation for the Therapeutic Area (TA) medical strategy.
• You will be responsible for conceptualizing and managing a wide range of medical activities, aligned with the TA Medical strategy, including research, publications, medical education, and patient support programs.
• You will be responsible for engaging key thought leaders through medical affairs activities, in line with the overall strategic plan.
• You will be responsible for ensuring the optimal execution of the strategic medical affairs plan through Regional Medical Affairs, encompassing medical education, product education, and special projects.
• You will be responsible for acting as a therapeutic area scientific expert, discussing scientific data with leading specialists, and providing training on the latest medical developments to the sales and marketing team.

PURPOSE:

• To support develop and implement global the medical initiatives across all markets for Toripalimab
• Evaluate the new assets under development at early stage of development from various sources including literature, BD & licensing opportunities to identify right products for the market.
• Connect with KOLs and conducting advisory boards for getting insight on therapy areas and the products under evaluations to arrive at right decision about product and help design strategy for launch of differentiated/new products.

Responsibilities:

1. Medical Affairs support for toripalimab for 21 markets

Support development of global medical strategy for Toripalimab acorss all indications

Provide scientific, medical, technical & clinical support for Toripalimab across launch markets

Build and disseminate medical insights in a regular basis with countries

Support with inputs and insights for RWE and HEOR studies for Toripalimab

1. Conducting Ad boards and KOL meetings / interactions to get Insights on Toripalimab and other NCE NBEs

Identify the need and plan the ad boards of other suitable meeting format to get insight about the identified differentiated/new product and around relevant disease area from KOLs.  Identifying KOLs, preparing the agenda of adbaord, and conducting adbaord and translating the insights into decision making pointer.

Guide country heads in process of identification, profiling and stratification of Key Opinion Leaders. Build Indication expansion plan insights for Toripalimab

1. Evaluation of products identified by BD teams

Support the evaluation of new product proposals identified by BD teams from medical perspective and contribute in overall decision making for the molecule.

1. Contribute towards development of clinical and regulatory pathways for Toripalimab /Innovative assets

In view of differentiated/new product, the position will provide medical inputs to cross functional team of Regulatory and clinical development.

1. Help in developing data generation plan and Post Marketing Studies for Toripalimab

Help in strategizing the data generation plan and help in developing the post marketing study (PMS) or RWE etc for the differentiated/new product to lead medical oncology. Analyse and suggest, if possible, improvements in the clinical trial design.

1. Support for medico-marketing activities: Additional medico-marketing activities for toripalimab such as delivery of medical training sessions to marketing & sales teams, review and approval of promotional materials and support for RWE studies & digital marketing initiatives as needed.

Job Summary
We are looking for experienced and dynamic Cluster Head (Chronic) in Medical Affairs team to actively contribute to the organization/business by taking people managerial responsibility and being responsible for the scientific, technical and ethical soundness of all policies, statements and endeavours. He/she will need to provide high quality and timely service in the areas of product commercialization/promotional support, interactions with healthcare professionals, continuing medical education, clinical research, sales force training, medical information, and performance/people management, and business support in the areas of new product development, regulatory affairs, quality standards, and information technology; alliance management may be included as applicable.

Roles & Responsibilities
• You will be responsible to provide tactical and strategic inputs, and business/technical expertise, to Product Management towards ethical promotion of assigned products, in the operational areas listed
• You will be responsible for providing strategic inputs for marketing and brand plans, overseeing the design and execution of medical-marketing programs, and facilitating interactions with healthcare professionals. Additionally, you will initiate, review, and approve promotional and educational materials while ensuring compliance with relevant SOPs, regulations, and industry codes.
• You will be responsible for developing, reviewing, and approving protocol documents and supporting materials for various clinical projects. Additionally, you will collaborate with Global Medical Affairs and Clinical Development, organize training sessions for project teams, and provide medical support for safety reporting and ongoing local studies. Furthermore, you will contribute to the planning and execution of Investigational New Drug Applications (NDAs).
• You will be responsible to provide useful, timely, accurate, and balanced medical information to internal (sales staff) and external customers.
• You will be responsible for training the Sales Force on basic sciences/assigned products and pre-launch and launch training for new products.
• You will assist the New Product Planning team in preparing business cases and pre-commercialization programs for global products, development of local formulations and line extensions. Additionally, you will provide support in market research, stakeholder mapping, and early access programs. You will also collaborate with various departments to evaluate commercial opportunities, including licensing, acquisitions, and co-promotion. 
• You will be responsible for providing medical and product expertise in the registration of new products/indications, as well as defending marketed products to various stakeholders. You will also oversee the writing and review of labelling documents and provide medical support for the processing of adverse event reports, adhering to relevant SOPs and practices.
• You will be responsible to develop and share expertise in identified medical and/or scientific therapeutic area, including but not limited to disease areas, markets, products (DRL products and key competitors) and services.
• You will be responsible to develop and share expertise in a specific medical/scientific subject, including protocol design, development, and training, Pharmacoeconomics, Outcomes Research, Health Technology Assessment, New Product Evaluation, Disease Management Programs, Intellectual Property Protection and Patents, and Medical Information
• You will be one-point Medical Affairs contact for Customer Relationship Management and operational liaison in the various functional domain.
• You will be responsible for fostering a culture of learning and development and managing the Medical Affairs staff, providing training, guidance, and support across various functional domains, ensuring adherence to company values and behaviours, and. 
• You will be responsible in budgeting, provisioning and expense control for the relevant Medical Vertical.

Looking for CIAM Platform experience resource who can guide the existing CIAM team on architecture, design and implementation standpoint. Candidate will be responsible for designing, implementing, and maintaining ForgeRock Identity and Access Management (IAM) solutions.

Specific responsibilities:

• Well versed in CIAM platform Architecture and should be able to Lead/guide CIAM teams on architecture, design and implementation standpoint
• Design, develop and implement ForgeRock Identity and Access Management solutions based on business requirements.
• Collaborate with Stakeholders to gather requirements, define IAM policies and design authentication and authorization workflows/Journey.
• Document design decisions, configurations and troubleshooting steps to facilitate knowledge sharing and ensure comprehensive system documentation.
• Integrate ForgeRock solutions with various applications and systems, ensuring seamless authentication and authorization processes.
• Develop and maintain custom scripts and connectors for ForgeRock products.

Requirement:

• Excellent problem-solving skills and ability to troubleshoot complex technical issues.
• Strong understanding of Identity Access Management concepts, protocols, and standards.
• Familiarity with modern authentication and authorization mechanisms, such as multifactor authentication, single sign-on and identity federation. (OAuth, OIDC, SAML, LDAP, and AD)
• Strong communication and collaboration skills, with the ability to work effectively in cross-functional teams and interact with stakeholders at all levels of organization.
• Certification in ForgeRock Identity Platform (ForgeRock Certified Identity Management Professional, ForgeRock Certified Access Management Professional) preferred
• Proficiency on Java programming language with experience on Java 8, Spring Boot, microservices.
• Experience with webservices (RESTful APIs, SOAP) and integration technologies (JSON, XML)
• Experience working in AWS Cloud environment especially on EKS, ECS etc.

The PrimeVigilance medical writer position offers a unique opportunity to further develop your career in the field of drug safety.

Key Responsibilities

• Independent authoring, editing and reviewing of various regulatory/clinical documents (e.g. aggregate reports, risk management plans and other documents needed throughout the product’s life cycle) with the responsibility for the quality and content of the document and compliance with internal and external standards
• Active participation in trainings and development, implementation and maintenance of quality system documents for medical writing, including internal templates and formats required for standardised documentation
• Support in all pharmacovigilance operations associated with medical writing
• Continuous self-education in all aspects associated with medical writing
•  

Purpose:

PV is primarily responsible for the oversight of and provision of medical input to benefit-risk assessment activities including: ad hoc data analysis in support of internal/external queries; preparation and review of aggregate reports; signal detection and evaluation; support of benefit-risk evaluation efforts; generation and/or review of risk management plans (RMPs), risk evaluation and mitigation strategies (REMS), identification of risk minimisation measures; handling of responses to Regulatory Authority queries, scientific/medical input to other safety related documentation including Health Hazard Evaluations, clinical study protocols, final study reports, dossier documents, Medical Affairs activities, commercial/marketing information, as needed and providing support for product labelling activities.

Main Responsibilities:

• Medical Review quality control (MRQC) of medical assessment of individual case safety reports (including coding, seriousness, expectedness, and company causality assessments) done by the vendor.
• Provide medical input and/or review of aggregate reports including: PSUR, PBRER, PADER, DSURs and ACOs.
• Conduct peer quality review of aggregate reports, and quality review of reports generated by the vendor.
• Signal management activities for assigned products, ensuring signal detection is conducted in a regular, timely manner in accordance with signal management schedule.
• Literature review for signal detection and validation.
• Signal validation report preparation. 
• Conduct aggregate safety data review on an ad hoc basis to support benefit-risk evaluations.
• Author/review RMPs and aRMM activities as required
• Prepare/review Health Hazard Evaluations and other ad hoc safety reports as requested.
• Labeling document review: provide medical input to reference safety information, Investigator Brochures, product labels and patient information leaflets to ensure the most up to date and accurate safety information is present in all labeling information.
• Regulatory Authority query management: liaise with Regulatory Affairs to respond to PV-related Regulatory Authority queries; coordinate with various stakeholders when finalizing the response, ensure responses are tracked to closure.
• Participate in development of CAPA and take ownership of CAPA completion as assigned.
• Participate in regular, scheduled meetings with PV team/service provider/third parties as required.
• Support for PV QMS: Support the development and revision of department SOPs and work instructions. And participate in the review of cross-functional SOPs which include reference to PV activities.
• Any other activity assigned by Global Head- Medical Assessment.

Relationship Management

• Working within PV team and cross-functionally with key stakeholder functions including Clinical, Regulatory Affairs, Medical Affairs, Commercial Teams and Business Units.
• Interactions with vendors/service providers for PV activities.

Process Improvement / Standardization

• Participate in process improvement initiatives under supervision of Head of Medical Assessment and Global Head of Pharmacovigilance to promote internal audit and regulatory inspection readiness.

Looking for CIAM Platform experience resource who can guide the existing CIAM team on architecture, design and implementation standpoint. Candidate will be responsible for designing, implementing, and maintaining ForgeRock Identity and Access Management (IAM) solutions.

Specific responsibilities:

• Well versed in CIAM platform Architecture and should be able to Lead/guide CIAM teams on architecture, design and implementation standpoint
• Design, develop and implement ForgeRock Identity and Access Management solutions based on business requirements.
• Collaborate with Stakeholders to gather requirements, define IAM policies and design authentication and authorization workflows/Journey.
• Document design decisions, configurations and troubleshooting steps to facilitate knowledge sharing and ensure comprehensive system documentation.
• Integrate ForgeRock solutions with various applications and systems, ensuring seamless authentication and authorization processes.
• Develop and maintain custom scripts and connectors for ForgeRock products.

Requirement:

• Excellent problem-solving skills and ability to troubleshoot complex technical issues.
• Required candidate with 5 - 7 years of experience.
• Strong understanding of Identity Access Management concepts, protocols, and standards.
• Familiarity with modern authentication and authorization mechanisms, such as multifactor authentication, single sign-on and identity federation. (OAuth, OIDC, SAML, LDAP, and AD)
• Strong communication and collaboration skills, with the ability to work effectively in cross-functional teams and interact with stakeholders at all levels of organization.
• Certification in ForgeRock Identity Platform (ForgeRock Certified Identity Management Professional, ForgeRock Certified Access Management Professional) preferred
• Proficiency on Java programming language with experience on Java 8, Spring Boot, microservices.
• Experience with webservices (RESTful APIs, SOAP) and integration technologies (JSON, XML)
• Experience working in AWS Cloud environment especially on EKS, ECS etc.

We are seeking Medical Information Associate to lead Dr. Reddy’s Medical Information Strategy and processes, including the daily oversight of Dr. Reddy’s product information database for US and Canada. The incumbent will be based in our India office and report to Head Pharmacovigilance & Medical Affairs - North America

Responsibilities:

• Develop high quality, scientifically sound medical information content (e.g., Medical Response Documents) to fulfill unsolicited requests for information from customers and to support achievement of established medical objectives

• Collaborate and coordinate with appropriate staff to provide guidance to the Medical Information Call Center (MICC) for appropriate handling of escalated inquiries and assist with training of the MIC as needed

• Support Associate MA NAG in performance of PRC related activities

• Assist in the development and review of medical information content to be provided to external customers in support of product access Collaborate with management and other internal stakeholders, to develop, implement, and maintain processes to maximize compliant and effective delivery of Medical Information services

• Serve as integral member of Medical Affairs Team In tandem with the Head of PV MA-NAG participate in post-launch activities ensuring Medical Information preparedness for successful product launches (launch documents, FAQs)

• Work independently yet ensure strategic alignment of information with key internal stakeholders and experts, as necessary

• Maintaining Medical Information SOPs and relevant vendor trainings

• Lead or participate in projects/initiatives within MI or across functions, as assigned

• Identify emerging medical trends, marketplace issues (e.g., Medical Inquiry Trends, Business Intelligence) and quality assurance issues and share with appropriate personnel

• Collaborate with relevant internal functions to maintain product information database

• Support the medical information needs of internal functions, as required, including Medical Affairs, Regulatory, and Pharmacovigilance

• Provide disease state and product training to internal groups as needed

• Support Medical Affairs activities as and when necessary and assigned by Head PV MA

• Vendor management

• Improve PVMA Database(s) efficiency by collaborating with MICC and internal stakeholders on optimization suggestions to meet growing demands of PVMA

• Provide suggestions on improving current technology or ways to maximize MIC database capabilities to help meet demands of PVMA function

   

The dedicated, full-stack CIAM, mid-level Senior Staff Engineer, should be able to partner, in building, enhancing and supporting our CIAM platform, in AWS cloud environment.

The incumbent should be able to perform all functions of software development and able to work both independently, and in team-oriented, collaborative environment, as well as work well under minimal direct supervision, selecting from a variety of established procedures, to accomplish assigned tasks.

Additionally, will be responsible for technical analysis, application development, application configuration, incident response and resolution, troubleshooting, testing, fixing bugs, source code management and executing and managing change processes and working collaboratively, with other application owners and cross-functional teams to understand business requirements and translate them into technical solutions.

Key Responsibilities:

• Customer Identity and Access Management (CIAM) mid-level Developer who, as part of CIAM team, will be responsible for the delivery of the Customer authentication platform and services required to support the various business lines
• Partner alongside application architects, to plan, design, develop and implement CIAM solutions, for API driven cloud and cloud/hybrid-based applications
• Design, configure, document, and enforce centralized CIAM architecture across multiple diverse business domains and application architectures, as part of CIAM team
• Provide required knowledge and expertise, to assist with the technical approach for the shared operational capabilities of CIAM, including user registration, self-service, authentication, authorization, administration, audit, and reporting
• Provide visible and sustainable CIAM services support maximizing value to customers and the business lines
• Designs, codes, tests, corrects, and web application in cloud, and assists in the implementation of software which forms part of a properly engineered information or communications system.
• Assists in providing accessibility, retrievability, security and protection of data in an ethical manner
• Defines test conditions for given requirements, test cases and creates test scripts and supporting data, working to the specifications provided
  • Interprets, executes and records test cases in accordance with project test plans
  • Analyzes and reports test activities and results
• Conducts tests as defined in an integration test specification, records the details of any failures, and carries out fault diagnosis relating to simple failures, reporting the results of the diagnosis in a clear and concise manner
• Assists as part of a team, on design of components of larger systems
• Supports integrated applications with an understanding of system integration, test planning, scripting, and troubleshooting
  • Establishes, participates, and maintains relationships with business units, customers and information technology subject matter experts in order to remain apprised of direction, project status, architectural and technology issues, risks, and functional/integration issues
• Willingness to step up, take initiatives and ownership