• Lead thoughtful, high‑value conversations with professionals exploring career growth or personal development • Support clients navigating transitions, promotions, leadership challenges or confidence barriers • Facilitate breakthroughs in clarity, communication and mindset • Apply your commercial and professional experience to guide clients effectively • Build and manage your own pipeline using proven marketing systems and training • Represent a global personal development brand with professionalism and care

• Deliver in-person and/or remote training sessions for client teams • Facilitate interactive workshops with a strong focus on engagement and participation • Adapt training delivery to local market context while maintaining global standards • Collaborate with CXG teams on training preparation and alignment • Support Train-the-Trainer sessions when required • Contribute to content localisation and continuous improvement of training materials • Engage confidently with client-facing teams and senior stakeholders.

• Provide an integral consultative component to our customer’s ongoing efforts to expedite the ROI and maximize the effectiveness of their business performance management solutions, especially OneStream XF. • Consultants are responsible for providing solutions by working with customers to develop applications primarily for financial reporting. • A Consultant completes the implementation work in a timely manner and can assist in validating the requirements and design of the application. • Act as an onboarding guide/mentor to new Consultants. • Produce project documentation including status reports, design documentation framework, application documentation, end-user training materials, test scripts, validation templates, etc. • Participate in Regional, North America, and Global practice calls.

Title: Medical consultant Location: Hyderabad Andhra Pradesh India Full time Remote Third Shift (Nights)   Join Us as a Pharmacovigilance Physician – Make an Impact at the Forefront of Innovation At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. The Pharmacovigilance Physician provides medical oversight of pharmacovigilance activities to ensure company SOPs, client directives, good clinical practice, and regulatory requirements are followed. Attends and presents at sponsor meetings, provides medical and pharmacovigilance consultation to clients and project team members. May also support business development activities. Provides medical review and analysis for clinical trial serious adverse events, marketed products ICSR with focus on triage, seriousness, expectedness, causality assessment, appropriate selection of adverse event terms using MedDRA terminology, narrative review and periodic safety reports (e.g. PBRER, PSUR, DSUR) as well as other client deliverables (e.g. labeling reconciliation documents, CTD modules, REMS, RMP, and CSR). Identifies and investigates safety signals and contributes to the management of the benefit-risk profile of assigned products. We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. What You'll Do: • Manage all medical aspects of contracted pharmacovigilance tasks across the pharmaceutical product life cycle. • Adhere to applicable regulations and ICH guidelines regarding clinical trials, regulatory documents, and safety issues, as well as client SOPs/directives, project-specific WPDs for assigned projects, and the organization’s corporate policies and SOPs/WPDs. • Provide medical consultation to team members and communicate clearly with associates and clients, maintaining an open line of communication to ensure all procedures are followed appropriately. • Provide therapeutic and protocol training on assigned studies, as requested. • Assist in writing (interpretation of safety data) and/or reviewing the safety portion of the CSR, IND/NDA report, ICSR, signal detection reports, periodic reports, RMP, REMS, CTD modules; scientifically review aggregate reports, contribute to label updates, review and assess literature, and support dossier maintenance and risk management activities to ensure that the medical content is accurate and complete. • Provide medical review of cases and perform reviews of adverse events of special interest and serious adverse events. • Perform data reviews as specified in the client contract and data validation manual, including review of coding listings and/or full safety data to assess potential safety concerns. Medically review adverse event and serious adverse event data from all sources (solicited, spontaneous, literature, etc.) as contracted. Education and Experience Requirements: • MD or equivalent or MBBS (with 2 years of clinical experience) required. Active medical licensure preferred. • Previous Clinical experience for MD or equivalent in treating patients for 2 years is desirable in the speciality or sub-speciality associated with the applicants training or experience in a Contract Research Organization, pharmaceutical company or experience as a principal investigator or direct experience in safety/pharmacovigilance that provides the knowledge, skills, and abilities to perform the job. In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills, Abilities: • Clinical expertise with attention to detail, quality and patient safety • Excellent medical knowledge of physiology and pharmacology, understanding of clinical study objectives and overview of the complete drug development process • Great multi-tasking abilities, technical, analytical, organizational and problem-solving skills, excellent oral and written communication skills, and presentation skills • Ability to work independently and under pressure, analyze work with attention to detail, process and prioritize sensitive complex information • Proficiency in basic computer applications • Fluent in spoken and written English • Excellent interpersonal, influencing and team building skills • Good understanding of FDA, ICH, EMA and GCP guidelines • Working knowledge of relevant safety databases, MedDRA, biostatistics, data management, and clinical operations procedures • Ability to act as a mentor/trainer to other staff