9738 Pharma Jobs - Page 49

Job Title Front End Engineer Job Description We re looking for Frontend Developer with expertise in Angular 18 team in Pune. Working for Signify - Horticulture Business unit in signify means being creative and adaptive. Our culture of continuous learning and commitment to diversity and inclusion creates an environment that allows you to build your skills and career. Together, we re transforming our industry. As the world leader in lighting, we re constantly ahead of the curve. Through our leadership in connected lighting and the Internet of Things, we re breaking new grounds in data analytics, AI, and smart homes, offices, cities and more! Signify is one of the few companies in the world to ...

Work Experience Required: 8 - 12 Years Experience in programing (Python, R, SQL, NoSQL,Spark) with ML tools & Cloud Technology (AWS, Azure, GCP) Experience in Python libraries such as numpy, pandas, scikit-learn, tensor-flow, scapy, scrapy, BERT etc. Good understanding in statistics, and ability to design statistical hypothesis testing to aid formal decision making. Develops predictive models using Machine Learning algorithms (SVM, Random Forest, Neural Network, Decision Tree, Logistic Regression, K-mean Clustering, linear regression, PCA etc.) Engaging with clients, understanding complex problem statements, and offering solutions in the domains of Retail, Pharma, Banking, Insurance, etc. Co...

Job Title Deputy Manager- Treasury Gurgaon office (Hybrid) Intro Summary of the Role This role is responsible for managing all treasury-related activities to ensure optimal liquidity, compliance, and financial risk management for the organization. The incumbent will handle cash flow planning, banking operations, foreign exchange transactions, and statutory compliance, while liaising with banks and internal stakeholders to support smooth business operations. Strong financial acumen, attention to detail, and stakeholder management skills are essential for success. What You Will Get Opportunity to manage treasury operations for a global life sciences leader. Exposure to strategic financial plan...

Use Your Power for Purpose At Pfizer, technology drives everything we do. You will play a pivotal role in implementing impactful and innovative technology solutions across all functions, from research to manufacturing. Whether you are digitizing drug discovery and development, identifying innovative solutions, or streamlining our processes, you will be making a significant impact on countless lives. What You Will Achieve Develop and lead/co-lead complex projects to achieve objectives. Coordinate with Solutions Delivery Engineers to identify opportunities for technology alignment and efficiency of implementation, executing process improvements. Act as the primary technical interface between t...

The Business Performance Services (BPS) department within GBS Enterprise Services was created to deliver services internally to Pfizer colleagues and divisions that help create room for meaningful work. By delivering our services with high performance against the Five Points of Value (i. e. optimal cost, quality, compliance, client experience, and business impact), we help colleagues spend more time focusing on their missions; all in support of breakthroughs that change patients lives. The services our team delivers include, data analytics, translations services, creative, training & development, contingent labor, et. al. We have a variety of vendors who provide these services; however, we h...

Job Title: Research Executive Function: R&D Location: Bangalore Unilever is reimagining the future of cleaning, and it starts with reinventing a century-old history of chemistry. Billions of people around the world are asking for products that are tough on germs and stains, and ever more convenient to use. But now, people also want these products to be kinder to the planet. The Purpose of the Science & Technology, Home care team is to provide Unilever with world class capability to develop next generation formats like powders, bars, liquids, capsule products with superior performance, great value, and sustainable technology. Within the S&T, team is responsible for exploring upstream/novel pr...

Compile and publish electronic regulatory submissions using publishing tools like Lorenz DocuBridge, Veeva Vault, and Extedo. Ensure compliance with eCTD standards, including bookmarks, hyperlinks, metadata, and validation. Perform quality control checks on submission components and final packages. Collaborate with cross-functional teams to gather and finalize documents. Maintain submission archives and ensure version control and traceability. Stay current with global regulatory guidelines and publishing best practices. Support audits and inspections by ensuring documentation integrity and readiness. Troubleshoot formatting and technical issues in submission documents and contribute to proce...

Provide scientific and medical input for early trial planning, start-up, recruitment, and retention. Monitor trial performance and proactively address scientific issues. Engage with site staff to ensure compliance and smooth trial conduct. Act as a local subject matter expert on products and protocols. Build and maintain relationships with Principal Investigators (PIs) and other key opinion leaders (KOLs). Communicate pipeline and scientific narratives effectively to internal and external stakeholders. Contribute to site selection, scientific training, and assessment of medical capabilities. Introduce Medical Affairs colleagues to KOLs and new therapy areas. Periodic travel to clinical trial...

Handle inbound calls from healthcare providers regarding medical claim review inquiries, denial reasons, and claim status updates. Review claim denial explanations and communicate next steps clearly and professionally to providers. Ensure compliance with internal claims review policies, organizational guidelines, and regulatory requirements. Demonstrate strong service quality and maintain accuracy in all claim-related communication. Collaborate with global counterparts to ensure consistent process execution and issue resolution. Follow all company policies, employment contract terms, and operational directives related to shift changes, reassignment, workflow modifications, and organizational...

Conduct thorough investigations into complex medical cases using strong analytical and problem-solving skills. Interpret and apply CPT guidelines, reimbursement policies, contracts, and clinical rules for claim review. Review pre-payment claims with medical records to assess accuracy and compliance. Participate in regulatory and client meetings to discuss clinical review findings and process improvements. Engage with providers, advocates, and legal teams to support resolution and reduce provider abrasion. Analyze data and support special projects, reporting, and operational enhancements. Job Requirements Certified Professional Coder (CPC) certification is mandatory. Strong knowledge of CPT a...

Manage affiliate mailbox and reconcile safety reports according to processes. Identify, create, and process Individual Case Safety Reports (ICSRs) in the safety database. Perform MedDRA coding and ensure accurate case documentation. Conduct follow-ups and ensure timely submissions as per regulatory guidelines. Adhere to client-specific SOPs, timelines, and quality standards. Handle routine issues based on established guidelines. Job Requirements Bachelor's or Master's degree in Pharmacy (B.Pharm/M.Pharm) or Life Sciences. Strong knowledge of pharmacovigilance basics and regulations. Experience with MedDRA coding and ICD-10 CM codes is preferred. Excellent communication and interpersonal skil...

Support the setup, administration, and maintenance of electronic Trial Master File (eTMF), IMPACT CTMS/eSTRA, and related clinical tools. Assist in project setup from initiation to closure, including site document collection, archiving, and quality control. Maintain study portals, version-controlled documents, and e-training records. Track project timelines and milestones, providing progress reports. Draft, update, and maintain key study documentation, SOPs, manuals, and training guides. Conduct file reviews and support internal/external audits to ensure document completeness and regulatory compliance. Job Requirements Bachelor's degree in Life Sciences, Pharmacy, or a related field. Possess...

Drive scientific strategy for clinical trial excellence and provide scientific and medical input for trial planning, start-up, recruitment, and retention. Monitor trial performance and proactively address scientific issues, acting as a local subject matter expert on products and protocols. Engage with site staff to ensure smooth trial conduct and build/maintain relationships with Principal Investigators (PIs) and other key opinion leaders (KOLs). Communicate pipeline and scientific narratives effectively and contribute to site selection, scientific training, and medical capability assessment. Support early portfolio strategy and pre-launch planning, introducing Medical Affairs colleagues to ...

Provide scientific and medical input for early trial planning, start-up, recruitment, and retention. Collaborate with Clinical Operations Therapy Area Leads and Trial Managers on clinical trial strategies. Monitor trial performance and proactively address scientific issues. Engage with site staff to ensure compliance and smooth trial conduct. Contribute to site selection, scientific training, and assessment of medical capabilities. Communicate pipeline and scientific narratives effectively to internal and external stakeholders. Job Requirements M.B.B.S with M.D. in a relevant discipline, strong clinical practice or research background. Minimum 4 years of experience in clinical or medical aff...

Conduct thorough investigations into claims to ensure accuracy and compliance with regulatory requirements. Review medical records and documentation to assess claim validity and identify potential issues. Analyze CPT/ICD coding guidelines and apply them to pre-payment claims. Collaborate with cross-functional teams to resolve complex claims-related issues. Develop and maintain expertise in clinical review processes and procedures. Identify areas for process improvement and implement changes to increase efficiency. Job Requirements Certified Professional Coder (CPC) certification is required; AAPC certification is an added advantage. Minimum 6 months of experience as a certified coder, prefer...

Develop training and drive change management for new global clinical trial regulations processes. Manage and coordinate redaction of clinical documents per EMA, Health Canada, EU CTR, and other regulations. Collaborate with Global Development Operations, Biostatisticians, Medical Writing, Submission Managers, and stakeholders to operationalize redaction requirements. Provide vendor and CRO oversight for document redaction and data sharing. Work with IT to implement technology solutions for clinical trial disclosure. Manage and track redaction book-of-work and compile performance metrics. Job Requirements MA/MS in a scientific or medical field is required; BA/BS with 5 years relevant scientif...

Review scales administered by raters to ensure standardized assessments. Conduct live interactions with raters to discuss methodology, scoring techniques, and provide guidance. Evaluate rater performance through mock interviews or functional assessments. Prepare for discussions with raters by evaluating case data and relevant scale items. Complete assigned rater interactions and tasks as scheduled. Submit documentation associated with tasks in a timely manner. Participate in orientation, training, and calibration activities. Maintain strong interpersonal skills to interact professionally with all levels of personnel and clients, providing guidance and feedback to ensure data reliability and ...

Participate in all required orientation, training, and calibration activities. Evaluate case data and prepare for rater discussions by reviewing scale items and preparing relevant documents. Conduct rater interactions and complete assigned tasks on schedule. Ensure timely submission of all documentation related to assigned tasks. Provide functional assessments of rater performance and assist with trial communications. Collaborate with cross-functional teams to achieve project goals. Job Requirements Minimum Master's degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work; MD, DO, or PhD preferred. Minimum 3 years of experience administering psychiatric assessments, rati...

Participate in all required orientation, training, and calibration activities. Review case data and prepare for discussions with raters, including understanding scale items and having necessary documents ready. Conduct rater interactions and complete assigned tasks according to schedule. Submit all required documentation on time. Administer psychiatric assessments, rating scales, or structured clinical interviews as part of the role. Engage in functional assessments such as mock interviews. Job Requirements Minimum Master's degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work; MD, DO, or PhD preferred. Minimum 3 years administering psychiatric assessments, rating sca...

Assist with site selection, document collection, and regulatory submissions. Conduct remote and onsite visits to ensure data accuracy and troubleshoot site issues. Ensure safety reporting processes, audit readiness, and adherence to protocols. Maintain study tables, trackers, and databases, ensuring TMF compliance. Participate in team meetings and contribute to study administration. Oversee site activities to ensure the collection of accurate, compliant data. Job Requirements Strong attention to detail, problem-solving, project management, technical writing, and communication skills. Degree in Pharma/scientific discipline or related Life Sciences field. High proficiency in English (spoken an...

Manage clinical trials from initiation to closeout, ensuring compliance with regulatory requirements and ICH GCP guidelines. Conduct site feasibility assessments and negotiate study budgets with sites. Ensure timely execution of clinical trial agreements and oversee site invoicing. Provide periodic updates on study progress, risks, and deliverables to stakeholders. Lead communication with cross-functional units to ensure efficient study conduct. Manage IMP supplies at sites and coordinate resupply orders. Ensure recruitment and retention strategies at sites are on track and mitigate study recruitment risks. Ensure compliance with PD & SAE reporting, audits, and inspections, performing site c...

Conduct qualification, initiation, monitoring, and closeout visits for research sites according to the approved protocol. Communicate with medical site staff, including coordinators and clinical research physicians. Verify investigator qualifications, training, resources, and site conditions. Review and verify medical records and research source documentation for accurate data reporting in compliance with the protocol. Ensure investigators are enrolling eligible subjects and review regulatory documents. Account for medical devices/investigational products and monitor adverse events and concomitant medications. Assess patient recruitment and retention efforts, providing suggestions for improv...

Oversee country and site selection, working with the Registries and Local Medical Affairs teams. Organize study materials, ethical and regulatory submissions, and ensure contracts and financial agreements. Maintain oversight of Registries, coordinate with Clinical Research Associates (CRAs), monitor contract issues, and track data quality. Ensure safety reporting and quality control, implementing Corrective and Preventive Actions (CAPA) as needed. Communicate effectively with stakeholders, providing updates and resolving issues promptly. Contribute to TMF compliance and maintain study tracking tools. Job Requirements A degree in Pharma or a scientific Life science discipline is required. Str...

Manage, mentor, and develop a team of clinical safety professionals. Cultivate and maintain strong relationships with clients and internal stakeholders by providing expert safety knowledge. Oversee clinical safety case management and aggregate reporting responsibilities for direct reports to meet client expectations with high quality. Create safety management plans tailored to client needs. Provide safety review of clinical study documents, including protocols, study reports, and marketing application components. Develop and implement effective safety strategies to ensure the safety of clinical trials. Job Requirements Bachelor's degree in a healthcare-related field (Nursing, Pharmacy, Pharm...

Assist the Project Manager in system design and setup for clinical studies. Create study-specific documents, including protocols, case report forms, and investigational reports. Track and provide key study metrics and project monitoring to stakeholders. Collaborate with clients to obtain requirements and respond to inquiries related to clinical trials. Handle other assigned projects and tasks, ensuring timely completion and quality delivery. Work closely with cross-functional teams to ensure compliance with regulatory requirements and company standards. Job Requirements Bachelor's degree in Life Sciences or a related field, such as B.Sc./ M.Sc./ M.Pharm/ B.Pharm. Proficiency in Excel and Wor...