18 Regulatory Processes Jobs

The responsibilities of the Clinical Research Associate at AstraZeneca involve ensuring the execution of Study Delivery processes by developing study reports tools, facilitating the study delivery system, and maintaining the system. As an expert in the field, you will be responsible for ensuring the delivery of a centrally managed study management service across clinical studies from start-up to reporting. Your role will also involve serving as the main contact and collaborating closely with the Document Management group until the Clinical Study Report is finalized. In addition, you will be responsible for initiating and maintaining the production of study documents, ensuring template and version compliance, as well as creating or importing clinical-regulatory documents into the Global Electronic Library according to the Global Document List. Collaboration with Data Management Center or Data Management Enablement representatives to facilitate the delivery of study-related documents will also be a part of your responsibilities. Managing and coordinating the tracking of study materials and equipment, monitoring administrative tasks during the study process, audits, and regulatory inspections according to company policies are also key aspects of the role. As a Clinical Research Associate, you will act as a technical owner within Patient Safety, demonstrating a deep understanding of processes and internal regulations. It is essential to keep your knowledge of best practices and new relevant developments up to date. Liaising with compliance team members to improve regulatory processes within the team and identifying opportunities to enhance the methodology and provide practical solutions for clinical development are also important responsibilities. Regarding People Management Responsibility, this role does not involve direct or indirect reports. The global remit for this position is limited to the own country. The ideal candidate for this position should possess a Bachelor's degree in a relevant discipline, experience in Study Management within a pharmaceutical or clinical background, and knowledge of relevant legislation and new developments in the area of Clinical Development and Study Management. Desirable qualifications include an advanced degree within the field, professional certification, and an understanding of multiple aspects within Study Management. Key relationships to reach solutions include internal interactions with the Study management function and other AstraZeneca employees, as well as external collaborations with external service providers and regulatory bodies. AstraZeneca is committed to creating an inclusive and diverse team representing all backgrounds and perspectives, with a focus on industry-leading skills. The company values diversity and equality of opportunity and welcomes applications from all qualified candidates, irrespective of their characteristics. AstraZeneca complies with all applicable laws and regulations on non-discrimination in employment and recruitment, as well as work authorization and employment eligibility verification requirements.,

You should be part-qualified as an accountant with strong analytical skills and well-established interpersonal and communication skills. Your experience should include knowledge of US and International Accounting Standards, as well as working with General Ledger systems such as SAP/4HANA. Familiarity with Statutory Financial statements application Workiva is preferred. Additionally, you must possess excellent team-working attitude and interpersonal skills. As a Chartered Accountant with Accounting experience, your main duties will include: - Controlling financial statements (income statement and balance sheet) and coordinating close checklist - Ensuring timely closure of books within monthly and quarterly deadlines - Maintaining communication with European Accounting and Location CFOs - Preparing and coordinating local financial statements - Handling Returns like Liquidity Monitoring, Receivable, Regulatory, and Tax related processes - Preparing decks for due diligence review - Reviewing and resolving assigned locations aged and reconciling items - Coordinating the preparation of various quarterly and year-end schedules - Participating in PwC process walkthroughs, SOX/ORP testing, and supporting GAO audits - Ensuring annual review of all procedures - Supporting MCRP testing, including spreadsheet control tasks Your role also includes understanding the fair treatment of customers and consistently incorporating it into your responsibilities as appropriate.,

As a Clinical Document Anonymization Specialist at GSK, your primary responsibility will involve preparing and anonymizing clinical documents in adherence to GSK's established standards. You will be tasked with ensuring meticulous documentation and oversight of all processes, procedures, and work instructions related to document anonymization to ensure compliance with regulatory requirements. Additionally, you will oversee and coordinate with external vendors and offshore service providers supporting the document anonymization and data sharing process. Your role will also involve monitoring the quality of information received from document anonymization partners through quality control and assurance efforts. You will play a crucial role in maintaining strong relationships with both external and internal business partners, effectively communicating to resolve issues hindering the disclosure of clinical documents and ensuring timely delivery as per agreed timelines and priorities. Your contribution will be essential in developing procedural and training documentation for document anonymization, as well as efforts to ensure the quality and consistency of anonymization standards and storage of clinical documents within the R&D framework. To be successful in this role, you should have a minimum of 4 years of experience in document anonymization, regulatory requirements, and stakeholder management. A Master's degree in life sciences is required, along with a solid understanding and prior experience in anonymization of clinical documents for EMA Policy 0070 and Health Canada PRCI. Experience in managing clinical trial activities, a good grasp of clinical trial lifecycle, metadata, and data, as well as excellent communication skills, attention to detail, and the ability to work independently are essential qualifications. Additionally, possessing a good understanding of R&D and clinical development processes, the ability to bridge communication gaps between scientific and non-scientific organizations, and manage conflicting demands in a high-pressure environment will be advantageous. Awareness of medical writing, publishing, and regulatory processes will also be beneficial to excel in this role. Join GSK, a global biopharma company dedicated to uniting science, technology, and talent to combat diseases and positively impact the health of billions worldwide. At GSK, we foster an environment where individuals can thrive, grow, and contribute to our mission of getting ahead of disease together. If you are motivated by our ambition and seek a place where you can be inspired, valued, and challenged to be your best, join us on this exciting journey to make a difference in healthcare. Please be advised that GSK does not accept referrals from employment businesses or agencies without prior written authorization. If you encounter unsolicited emails or job advertisements not from gsk.com, kindly disregard them and reach out to us at askus@gsk.com for verification of job authenticity.,

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today! Job Details Develop and maintain client relationships and highlight opportunities for increased service support to the respective lead. Participation in regulatory processes to gain and maintain marketing authorizations for human and veterinary medicinal products (applications, renewals, variations) including medical devices, cosmetics, food supplements and herbal products with emphasis on CMC aspects. Support with preparation, review and compilation of CMC documents within the framework of regulatory affairs projects. Communicate with clients and Health Authorities in close cooperation with the respective lead. Support with the planning and execution of client projects in accordance with KPIs in close cooperation with the respective lead. General guidance (consultancy) of colleagues and clients regarding CMC Services. Regulatory intelligence - develop and maintain personal regulatory knowledge, apply to client projects and actively share with colleagues. Support with VDC strategy implementation and optimization. Comply with and support the maintenance of internal procedures. Provide operational insights to support with VDC led commercial, marketing and business development activities including proposal input in close cooperation with the respective lead. Support respective lead in delivery to budget with accurate and timely reporting and provide project insights to address invoicing queries. In agreement with Head of VDC REG providing on-site regulatory support to GCS clients. The employee agrees to take over other reasonable tasks that are corresponding with their abilities upon agreement with their Line Manager/Practice Area Lead/Head of VDC REG. Handling of M3 databases Compilation/handling of wToCs for renewals/variations Drafting of eAFs and country information letters for dispatch packages Communication with local affiliates regarding local requirements Change assessments according to EU variation guideline CMC background preferred, IT affinity, very detail oriented, excellent communication skills Maintain knowledge and understanding of SOPs and current regulatory guidelines as applicable. What Cencora offers Benefit offerings outside the US may vary by country and will be aligned to local market practice. The eligibility and effective date may differ for some benefits and for team members covered under collective bargaining agreements. Full time Affiliated Companies Affiliated Companies: PharmaLex India Private Limited Equal Employment Opportunity Cencora is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status or membership in any other class protected by federal, state or local law. The companys continued success depends on the full and effective utilization of qualified individuals. Therefore, harassment is prohibited and all matters related to recruiting, training, compensation, benefits, promotions and transfers comply with equal opportunity principles and are non-discriminatory. Cencora is committed to providing reasonable accommodations to individuals with disabilities during the employment process which are consistent with legal requirements. If you wish to request an accommodation while seeking employment, please call 888.692.2272 or email [HIDDEN TEXT]. We will make accommodation determinations on a request-by-request basis. Messages and emails regarding anything other than accommodations requests will not be returned Show more Show less

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today! Job Details Develop and maintain client relationships and highlight opportunities for increased service support to the respective lead. Participation in regulatory processes to gain and maintain marketing authorizations for human and veterinary medicinal products (applications, renewals, variations) including medical devices, cosmetics, food supplements and herbal products with emphasis on CMC aspects. Support with preparation, review and compilation of CMC documents within the framework of regulatory affairs projects. Communicate with clients and Health Authorities in close cooperation with the respective lead. Support with the planning and execution of client projects in accordance with KPIs in close cooperation with the respective lead. General guidance (consultancy) of colleagues and clients regarding CMC Services. Regulatory intelligence - develop and maintain personal regulatory knowledge, apply to client projects and actively share with colleagues. Support with VDC strategy implementation and optimization. Comply with and support the maintenance of internal procedures. Provide operational insights to support with VDC led commercial, marketing and business development activities including proposal input in close cooperation with the respective lead. Support respective lead in delivery to budget with accurate and timely reporting and provide project insights to address invoicing queries. In agreement with Head of VDC REG providing on-site regulatory support to GCS clients. The employee agrees to take over other reasonable tasks that are corresponding with their abilities upon agreement with their Line Manager/Practice Area Lead/Head of VDC REG. Experience and Educational Requirements Several years experience, or demonstrable capability, in area of responsibility on similar field; advanced knowledge and insights required to perform processes efficiently and proven potential to take over more complex tasks. University degree in Life Science. Minimum Skills, Knowledge and Ability Requirements Ability to deliver on customer or internal projects / processes within daily work; ability to prioritize parallel tasks, escalate issues where appropriate and to offer solutions for appropriate counter measures. Structured and systematic and independent way of working; limited latitude within established set of procedures, may determine priorities with little supervision. Ability to analyze and solve problems and to offer solutions for a given task or project. Attention to detail. High service orientation Ability to train and support junior/new colleagues in daily activities; ability to lead small projects with clearly defined scope. Ability to manage internal and external (client) relationships on operational / day-today working level as well as client&aposs team lead level. Good communication skills (written and verbally); capability to communicate issues and propose solutions. Confident appearance. English business fluent What Cencora offers Benefit offerings outside the US may vary by country and will be aligned to local market practice. The eligibility and effective date may differ for some benefits and for team members covered under collective bargaining agreements. Full time Affiliated Companies Affiliated Companies: PharmaLex India Private Limited Equal Employment Opportunity Cencora is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status or membership in any other class protected by federal, state or local law. The companys continued success depends on the full and effective utilization of qualified individuals. Therefore, harassment is prohibited and all matters related to recruiting, training, compensation, benefits, promotions and transfers comply with equal opportunity principles and are non-discriminatory. Cencora is committed to providing reasonable accommodations to individuals with disabilities during the employment process which are consistent with legal requirements. If you wish to request an accommodation while seeking employment, please call 888.692.2272 or email [HIDDEN TEXT]. We will make accommodation determinations on a request-by-request basis. Messages and emails regarding anything other than accommodations requests will not be returned Show more Show less

As a Delivery & Relationship Manager - BFSI at iSolve, your role will involve being the primary point of contact between the customer and our organization. You will represent the Voice of the Customer within iSolve, ensuring that customer needs, expectations, and concerns are effectively communicated and addressed. In this dynamic role that involves working both at customer sites and in the office in Chennai, you will be responsible for managing relationships with up to 5 key customers. Your goal will be to enhance these relationships, meet the benefit objectives of the customers, and contribute to the revenue goals of iSolve. Customer Side Responsibilities: - Understand and clarify customer requirements, expectations, and deadlines comprehensively. - Take the lead in project management at the customer side, engaging with key stakeholders and decision-makers. - Coordinate and deliver projects within set timelines, budget constraints, and quality standards. - Oversee platform deployment and Go Live activities, managing post-implementation expectations. - Communicate effectively with customer teams on technology, IT security, and project delivery matters. - Establish robust project governance and monitoring processes, ensuring clear communication on project milestones, issues, and resolutions. - Act as the main point of contact for assigned clients, fostering strong relationships and aligning business objectives. - Provide strategic guidance to clients, helping them achieve their growth goals. - Monitor customer needs and collaborate with iSolve's product teams to address evolving requirements. - Ensure high levels of customer satisfaction and happiness. iSolve Side Responsibilities: Delivery & Deployment: - Represent customer expectations accurately to iSolve's Business Analytics and Development teams. - Lead projects from initiation to closure, ensuring alignment with customer success criteria. - Manage customer expectations, escalations, and communications in a proactive and professional manner. - Guide iSolve teams to meet customer expectations in project completion and deployment. - Ensure that iSolve's performance exceeds established KPIs. Farming Sales, Renewals, and Cross-Sells: - Achieve business growth targets and financial goals for assigned customers. - Proactively identify and capitalize on new sales opportunities, renewals, and cross-selling prospects. - Prepare for customer-side changes and expansion plans, engaging with decision-makers and influencers. - Establish relationships with customer executives through proactive engagement activities. - Collaborate with internal teams to develop tailored solutions for customers. - Accountable for P&L management, revenue forecasting, and success strategies. Knowledge and Skills Required: - Positive attitude and growth mindset. - Proficiency in BFSI domain and regulatory processes. - Strong project management skills and experience with methodologies and tools. - Excellent communication and interpersonal skills. - Leadership abilities to motivate cross-functional teams. - Problem-solving and decision-making skills. - Knowledge of SDLC processes and best practices. - Relevant certifications like PMP, Scrum Master are advantageous. - Experience in client relationship management and business development. Education and Experience: - Masters degree in any discipline. - Minimum 5 years of experience in Delivery, Last Mile deployment, and Customer Engagement. - Experience in BFSI domain and technical project management. If you are passionate about customer engagement, possess a deep understanding of the BFSI domain, and have a track record of successful client relationship management, we encourage you to apply for this exciting opportunity at iSolve. For further details or to apply, kindly contact HR - Mr. Vinodh at 89398 32456. This is a full-time position with benefits including health insurance, provident fund, performance bonuses, and yearly bonuses. The work schedule is during day and morning shifts.,

As the Head of Business Development at Medifodil Smart Pharma Solutions, you will play a crucial role in leading the organization's business growth initiatives. Your primary focus will be on driving lead generation, client acquisition, and revenue generation by converting opportunities into long-term business partnerships. Your key responsibilities will include identifying, building, developing, and growing new business streams and clients in both Indian and International markets. You will be responsible for driving lead generation strategies, identifying potential clients in pharma, biotech, and healthcare sectors, and converting leads into signed contracts through effective communication and proposal pitching. Building and maintaining strong client relationships, preparing compelling business proposals, and collaborating with internal teams to align services with client expectations will also be part of your role. To be successful in this position, you should have a proven track record of generating and closing B2B deals in the CRO/pharma space. A deep understanding of clinical research services, strong negotiation, communication, and presentation skills, as well as strategic thinking with an execution mindset are essential. Familiarity with CRM systems and BD tools will be an added advantage. Ideally, you should hold a Bachelor's or Master's degree in Life Sciences, Pharmacy, or Business Administration, and have a minimum of 10 years of relevant business development experience in the CRO/pharmaceutical industry. If you are ready to take on this challenging role and meet or exceed monthly and quarterly business targets, we encourage you to send your CV and a brief cover letter to careers@medifodil.com with the subject line: Application for Business Development Head. Join us in our mission to provide quality-driven, end-to-end research services and compliance support to pharmaceutical and biotech companies worldwide.,

As the Head of the Business Transformation Office at GSK, you will lead strategic initiatives to revolutionize clinical operations through technology, innovation, and process optimization. Your role will be crucial in shaping strategies, enabling change, and delivering impactful solutions that accelerate clinical trials and enhance patient outcomes. Your responsibilities will include defining and implementing the strategic transformation of clinical operations processes and technologies. You will collaborate with senior leadership to envision the future state of clinical operations, oversee project management, financial approvals, and funding requests for digital and transformation initiatives. Additionally, you will lead a team of change and value management professionals to embed people, process, and technology changes effectively. In this role, you will develop and track KPIs to measure the success of transformation initiatives, manage governance for tech programs, secure and manage budgets for technology transformation, and build consensus and foster collaboration across Clinical Operations, Research Units, and other stakeholders. You will also translate strategy into actionable plans and operational implementation and serve as a key member of the Development Analytics Platform Leadership Team (DAP LT). To be successful in this position, you should have a Bachelor's degree in computer science, information technology, life sciences, or a related field, along with 10+ years of experience in business transformation, project management, or change management within drug development. Proven expertise in clinical development, regulatory, and quality processes, as well as leadership and team management experience, are essential. An advanced degree (MS, PhD, or MBA) in a relevant field is preferred, along with exceptional leadership, team management, and influencing skills. Your ability to deliver high-quality results while managing complex challenges, experience with implementing change initiatives and leading organizational transformation, familiarity with governance processes, and chairing high-level meetings will be advantageous. Strategic thinking, strong influencing skills, expertise in storytelling, and exceptional communication skills will also be key to your success in this role. Join us at GSK in uniting science, technology, and talent to advance healthcare and make a positive impact on the lives of billions of people. We believe in creating a culture where employees can thrive and be themselves, feeling welcomed, valued, and included. If you share our ambition, we invite you to be a part of our exciting journey forward together.,

As a Senior Relationship Manager at JM Financial Home Loans, located in Erode, you will play a crucial role in managing and nurturing client relationships, offering expert guidance on home loans, and ensuring a smooth loan application and disbursement process. Your responsibilities will include conducting client consultations, reviewing documentation, processing loan applications, and addressing customer inquiries. Upholding a high standard of customer satisfaction and striving to meet or surpass sales targets will be key aspects of your role. To excel in this position, you should possess experience in client relationship management and customer service, a sound understanding of home loan products and loan processing, and proficient communication, negotiation, and interpersonal skills. The ability to work autonomously while managing multiple clients concurrently, along with strong sales and marketing acumen geared towards achieving targets, is essential. Familiarity with financial documentation and regulatory procedures is advantageous. A Bachelor's degree in Finance, Business Administration, or a related field is required for this role. Prior experience in the housing finance industry would be beneficial, though not mandatory. Join us at JM Financial Home Loans and contribute towards making home ownership dreams a reality while delivering exceptional service to our valued clients.,

We are seeking an experienced Solar Project Manager to oversee solar energy projects throughout the entire lifecycle, from initial planning to final commissioning. As the Solar Project Manager, you will be responsible for managing project timelines, budgets, quality standards, and ensuring compliance with regulations. Your role will involve collaborating with clients, engineers, vendors, and regulatory bodies to successfully deliver solar projects. Key Responsibilities: - Develop and execute project plans to deliver solar projects within defined scope, budget, and schedule. - Obtain necessary permits, approvals, and ensure regulatory compliance for solar projects. - Monitor project budgets, control costs, and optimize the utilization of available resources. - Manage procurement activities, negotiate contracts with vendors, and oversee vendor relationships. - Ensure that safety, environmental, and performance standards are met throughout project execution. - Maintain comprehensive project documentation and provide progress updates to stakeholders. Qualifications: - Bachelor's or Master's degree in Renewable Energy or Project Management. - Minimum of 7 years of experience in managing solar projects. - In-depth knowledge of solar energy systems and project management tools. - Strong leadership, organizational, and communication skills. This is a full-time, permanent position that offers benefits such as commuter assistance, health insurance, and Provident Fund. The work location for this role is in person. Kindly note that the job types include Full-time and Permanent.,

You will be joining Star Union Dai-ichi Life Insurance (SUD Life) as a Team Leader based in Gorakhpur. In this full-time on-site role, your primary responsibilities will include managing and supervising a team, ensuring the team achieves sales targets, and providing necessary training and support to team members. You will be required to monitor team performance, conduct regular reviews, and implement strategies to enhance productivity. It will also be your duty to uphold compliance with company policies and industry regulations. To excel in this role, you should possess strong leadership and team management skills, along with previous sales experience, preferably in the insurance sector. Effective communication and interpersonal abilities are essential, as well as being goal-oriented with excellent problem-solving skills. Proficiency in utilizing sales management tools and software is a must, and the capability to provide training and development to team members is crucial. Prior experience in compliance and regulatory processes would be advantageous. A Bachelor's degree in Business Administration, Finance, or a related field is preferred to qualify for this position. If you are an ambitious individual who thrives in a growth-oriented environment, this opportunity at SUD Life may be the perfect fit for you.,

As a Relationship Manager specializing in High Net Worth (HNI) clients, your primary responsibility will be to develop new customer relationships within the priority business segment. This will involve conducting in-depth profiling of clients to identify opportunities and effectively match these opportunities to our range of products and solutions. Your goal will be to meet with clients in person to understand their financial goals and needs, providing tailored recommendations for appropriate investment products. In order to achieve this, you will be required to formulate and execute a comprehensive sales plan aimed at acquiring new HNI clients and expanding our customer base. Drawing on your investment expertise, you will conduct portfolio reviews for clients and present suitable products based on their individual requirements. Resolving client queries within the specified turnaround time and ensuring a high level of customer service will be crucial aspects of your role. As a Relationship Manager, you will also be expected to plan and execute special sales initiatives and events for both prospective and existing clients. Maintaining detailed records of client relationships, adhering to regulatory processes, and upholding the bank's customer service standards will be essential components of your day-to-day responsibilities. Job Requirements: - Demonstrate aptitude for delivering high-quality customer service through effective organization and interpersonal skills. - Possess NISM certification (IRDA certification preferred). - Exhibit fluent communication skills, a presentable demeanor, and a quick grasping power. - Showcase strong decision-making abilities and a sense of ownership in understanding and fulfilling client requirements. - Have proven expertise in portfolio management for high net worth clients and relationship building. - Preferably have experience in banking or NBFC with a strong background in portfolio management. Experience: You should have a minimum of 5 years of experience in relationship and portfolio management to be considered for this role.,

As a Senior Manager Pre Sales for Financial Risk Management at Capgemini Invent, you will utilize your 12-15 years of experience to drive the Data-driven FRC Pre-Sales track. Your primary responsibilities will include leading pre-sales activities, engaging with clients to understand their business goals, and delivering high-quality experiences throughout the engagement process. You will be expected to create offers, client pitches, and business proposals, as well as respond to RFQs/RFPs to support the sales team in closing deals efficiently. In your domain role, you will leverage your expertise in measuring credit, market, and liquidity risks to provide advisory services to clients. You should demonstrate deep technical knowledge of financial products, lead client engagements effectively, and stay updated on market trends within the financial services sector. Additionally, you will be responsible for managing risk, communicating with stakeholders, and contributing to the development of consulting assets to support pre-sales activities. To excel in this role, you should possess relevant experience in the financial services industry, with a strong focus on front office sales and trading, risk management, and regulatory requirements. Your ability to communicate effectively, create compelling presentations, and interact with diverse audiences will be crucial. Proficiency in Microsoft PowerPoint and other MS Office tools is essential, along with the capability to manage complex projects and multitask efficiently. A Bachelor's degree with 12+ years of relevant work experience or a Master's degree with 10+ years of experience is required for this position. Certifications such as FRM, CQF, CFA, PRM, and knowledge/experience with Risk Management platforms will be beneficial. Strong verbal and written communication skills, problem-solving abilities, and a passion for customer-facing roles are key attributes we are looking for in a candidate for this role. If you are a proactive and results-driven professional with a keen interest in financial risk management and pre-sales activities, we encourage you to apply for this exciting opportunity to join our dynamic team at Capgemini Invent.,

The lead Program Management, Small Molecules position is responsible for establishing and providing overall leadership in project management for small molecules technology (SMT) and Analytical technology (AT) in Chennai, as well as supporting the management of OpEx and CapEx budgets. This role also involves supporting Stores & Logistics for the synergy site. You will provide leadership to the Project Management team by defining clear, realistic goals, removing barriers to ensure team progress, and facilitating rapid decision-making. Additionally, you will facilitate resolution and appropriate escalation of conflicts within the team and with other stakeholders to ensure project success. Managing internal and external business partners to achieve common objectives is a critical responsibility, along with engaging, influencing, and coordinating all functions involved in the development of assigned products. Collaboration with other functions in the organization is essential to ensure stakeholders" requirements are addressed and met appropriately. You will work towards establishing program goals and milestones that align with Pfizer's overall business strategy, monitoring existing processes and proposing or implementing changes when needed. Identifying and resolving potential issues that impact the portfolio, as well as managing resources, budgets, and effective governance meetings, are key aspects of this role. As the ideal candidate, you should hold a Master of Science (MSc) or Doctor of Philosophy (PhD) in a scientific or technical field related to Chemistry or Chemical Engineering. With over 15 years of experience in scientific and technical project management within the pharmaceutical sector, you should possess advanced project management skills, hands-on experience with drug regulations, and the ability to manage a portfolio of projects. Must-have qualifications include familiarity with small molecule manufacturing technologies, excellent leadership skills, and a proven track record in technical project management. Additionally, you should be an active listener, capable of synthesizing complex information into clear priorities, and maintaining technical and project management capability within the Technical Teams. Preferred qualifications such as PMP certification and experience with the Power BI tool are considered advantageous. This role will involve interactions with various internal and external stakeholders, including Small Molecule Technology, Analytical Technology, Global Technology Engineering & Launch, Pfizer Manufacturing Sites, and Regulatory Sciences. The work location assignment for this position is Hybrid. Pfizer is an equal opportunity employer that complies with all applicable equal employment opportunity legislation in each jurisdiction of operation.,

YASH Technologies is a leading technology integrator specializing in helping clients reimagine operating models, enhance competitiveness, optimize costs, foster exceptional stakeholder experiences, and drive business transformation. At YASH, you will be part of a team of bright individuals working with cutting-edge technologies. Our purpose is to bring about real positive changes in an increasingly virtual world, transcending generational gaps and disruptions of the future. We are currently seeking Banking, Financial Services, and Insurance Professionals to join us in the following areas: **Digital** - Develop Digital/Business Transformation Roadmaps - Implement Digital Products and Digital Service offerings as a Business Analyst through agile practices - Create Customer Service/Customer Delight Transformation Roadmaps - Engage in strategy development, global benchmarking, internal benchmarking, and Industry Points of View - Manage stakeholders, analyze impacts, and conduct business benefit analysis - Create Process Maps and foster cross-functional understanding - Transform processes including measurement techniques (Design thinking, SIPOC) - Perform Financial Modelling of benefits - Participate in business development efforts, including proposal development and client presentations **Domain** - Act as the primary domain expert in underwriting, claims, operations, reinsurance, actuarial, financial, and regulatory processes - Provide strategic guidance to internal teams and leadership - Lead and support digital transformation projects, incorporating automated underwriting, AI-driven claims processing, and digitalization of legacy systems - Analyze and interpret key business metrics to drive operational excellence - Collaborate with cross-functional teams to design and implement insurance solutions and workflows - Stay updated on industry trends, regulatory changes, and emerging technologies - Conduct knowledge sharing sessions and training for new joiners and stakeholders - Communicate effectively with external partners, reinsurers, and auditors - Identify and escalate opportunities for process improvement and operational efficiency **Qualifications and Education Requirements** - Bachelor's/Master's degree in Insurance, Actuarial Science, Finance, Business, or related field - 10+ years of experience in the insurance industry with expertise in underwriting, claims, reinsurance, actuarial, financial, and regulatory processes - Proven track record in supporting or leading digital transformation initiatives within insurance - Strong analytical skills and familiarity with insurance KPIs and business metrics - Excellent communication, stakeholder management, and training skills - Up-to-date knowledge of insurance regulations, products, and industry best practices - Ability to work with Tech/Digital tools, handle large data, and travel as required At YASH, you will have the opportunity to build a career in an inclusive team environment. We offer career-oriented skilling models and utilize technology for continuous learning and growth. Our workplace is grounded in flexible work arrangements, emotional positivity, transparency, open collaboration, support for business goals, and a stable employment with an ethical corporate culture.,

The Technology Service Analyst, NCT position in Pune, India involves working in the eDiscovery Operations team, responsible for capturing, retaining, recovering, and transferring electronically stored information. The role focuses on identifying process platforms and recovering data from various sources to meet legal, compliance, and regulatory requirements for internal and external stakeholders. Attention to detail is crucial to ensure accuracy and completeness of data provided to requestors. The position offers a range of benefits under a flexible scheme, such as a comprehensive leave policy, gender-neutral parental leaves, childcare assistance benefit, sponsorship for industry certifications, employee assistance program, hospitalization and life insurance, and health screening. Key responsibilities include preserving data in compliance with legal requirements, collecting data in a defensible manner, maintaining accurate record-keeping, utilizing software for handling data from different sources, ensuring confidentiality, contributing to business change solutions, ensuring process assurance, collaborating with stakeholders, providing technical analysis, offering consultative guidance, building relationships, managing operational performance, providing management information, and driving CSR initiatives. The ideal candidate should have at least 6 years of experience in data handling or IT support roles within eDiscovery, familiarity with forensic technologies and workflows, attorney document review processes, technical incident management, enterprise-level infrastructure, messaging technology, database concepts, incident management tools, secure environments, chain of custody requirements, eDiscovery investigation, and global collaboration. Knowledge of Service Delivery concepts through Six Sigma or ITIL certification is preferred. Support for the role includes training, coaching, continuous learning opportunities, and a range of flexible benefits. The company promotes a culture of excellence, responsibility, commercial thinking, initiative, and collaboration, striving for success together as the Deutsche Bank Group. For more information about the company, visit: [https://www.db.com/company/company.htm](https://www.db.com/company/company.htm),

As a Senior Manager Pre Sales for Compliance for Industries at Capgemini Invent, you will leverage your 12-15 years of experience to play a crucial role in the Data-driven FRC Pre-Sales track. Your responsibilities will include engaging in pre-sales activities, conducting initial client communication, and understanding the business objectives of our clients. You will be presenting and demonstrating our capabilities to prospective clients, creating business proposals, responding to RFQs/RFPs, and developing proofs-of-concept to support the sales team in closing deals. Your domain role will involve conducting industry analysis in the life sciences sector, creating industry reports, providing updates on regulatory changes, and staying informed about compliance landscapes globally. You will collaborate with internal teams/partners, lead the development of consulting assets, and support pre-sales activities and capability demonstrations. In addition to your pre-sales responsibilities, you will assist in managing GRC projects, optimize supply chain processes, monitor project KPIs, and utilize data analytics to measure compliance program effectiveness. Your proficiency in Microsoft PowerPoint will be essential for creating professional presentations and effectively communicating findings to diverse audiences. To excel in this role, you should possess strong communication skills, project management abilities, knowledge of regulatory processes, and the willingness to engage in customer-facing roles. A background in technology consulting, familiarity with regulatory platforms, and a passion for addressing client pain points will be advantageous. Your qualifications should include a Bachelor's or Master's degree in a relevant field, along with 6-8 years of experience in a pre-sales role. Proficiency in MS Office applications and a valid Business Visa for potential US travel are also required. If you are ready to take on this challenging yet rewarding role, apply now to be part of our dynamic team at Capgemini Invent.,

This role is responsible for leading and managing a multidisciplinary cross-functional Clinical Trial Team (CTT) or supporting the Sr. CPM in effective planning, re-evaluation, and implementation of assigned clinical studies and programs. The main focus is on ensuring adherence to timelines, budget, quality standards, and operational procedures as per Novartis Global processes. Key Responsibilities: - Agreeing with colleague/customer team and Line Functions on realistic project and study timelines and escalating issues if no agreement is achieved. - Leading and managing a multidisciplinary cross-functional Clinical Trial Team in planning, re-evaluation, and implementation of clinical studies and programs. - Supporting or leading other projects/programs in collaboration with cross-functional teams. - Organizing investigators meetings and internal meetings related to clinical study execution and operational excellence. - Interacting with investigator sites, CRAs/CROs/vendors to ensure smooth study set up and conduct, reviewing site performance, protocol deviations, risk assessment, and issue resolution. - Supporting compilation of study regulatory documents for submissions to authorities and ethics committees. - Supporting clinical studies with monitoring activities, communications, and quality control of monitoring activities. Essential Requirements: - Approximately 8 years of Global Clinical Operations experience with managerial experience in designing, planning, executing, reporting, and publishing clinical studies. - Proven ability to work independently in a complex matrix environment and lead cross-functional teams. Desirable Requirements: - Solid project management skills. - Thorough knowledge of Good Clinical Practice, clinical study design, statistics, regulatory processes, and global clinical development. - Demonstrated presentation, diplomacy, negotiation, conflict resolution skills. - Strong customer-oriented mindset and willingness to act accountably in project/study management. Novartis is committed to diversity and inclusion in the work environment and building diverse teams that represent the patients and communities served. Join our Novartis Network to stay connected and learn about suitable career opportunities as they arise.,