1760 Ich Jobs - Page 2

Supervise and prepare high-quality regulatory submissions to meet company timelines and guidelines. Evaluate complex regulatory issues and provide accurate and timely recommendations. Manage life cycle management activities, including variations, renewals, and responses to health authority queries. Establish and maintain regulatory strategies for submissions and manage document deliverables. Oversee regulatory or team databases and trackers, updating them when necessary. Collaborate with cross-functional teams to ensure timely submission and maintain stakeholder partnerships. Job Requirements Pharm D/MS in a scientific discipline or equivalent education and related experience. Minimum 10 yea...

We are looking for a skilled Process Coach to join our team at Omega Healthcare Management Services Pvt. Ltd., responsible for coding and ensuring the quality of healthcare services. The ideal candidate will have a strong background in healthcare management and excellent coaching skills. Roles and Responsibility Develop and implement process improvements to increase efficiency and productivity. Collaborate with cross-functional teams to identify areas for improvement and implement changes. Provide training and support to staff on new processes and procedures. Monitor and analyze performance metrics to ensure compliance with industry standards. Identify and mitigate risks associated with proc...

Conduct thorough causal assessments of adverse events and medical conditions. Develop and implement effective clinical SAS programming strategies for data analysis. Collaborate with cross-functional teams to ensure compliance with GCP guidelines. Utilize expertise in ICD-10 CM codes, CPT-Codes, and HCPCS Codes for accurate data management. Apply knowledge of ICH guidelines and MedDRA coding principles to drive business outcomes. Provide exceptional customer service through effective communication skills. Job Requirements Bachelor's degree in B.Sc, M.Sc, B.Pharm, or Master's degree in Pharmacy (M.Pharma) or MBBS. Strong understanding of pharmacovigilance processes, including causality assessm...

Coordinate and manage clinical trials from initiation to completion. Develop and implement study protocols and case report forms. Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Conduct site feasibility assessments and coordinate site monitoring activities. Manage and analyze clinical trial data. Ensure timely and accurate reporting of clinical trial results. Job Requirements Bachelor's or Master's degree in Pharmacy (B.Pharm/M.Pharm) or B.Sc./M.Sc. Minimum 2 years of experience in clinical research. Strong knowledge of GCP guidelines, ICD-10 CM codes, CPT codes, and HCPCS codes. Excellent communication and interpersonal skills. Ability to work inde...

Support the maintenance and optimization of Clinical Operations systems. Collaborate on creating and optimizing training programs related to clinical systems. Act as a backup Clinical Business Administrator for system-related activities including CTMS and eTMF administration. Monitor and ensure adherence to Clinical Operations policies and SOPs to maintain inspection readiness. Assist in identifying process challenges and suggesting technology-driven improvements. Contribute to project plans and system-related activities. Job Requirements Bachelor's degree in science, nursing, or a related field. Minimum 3 years of experience in a Clinical Study Manager role or related GCP procedures work. P...

Conduct causality assessments and clinical SAS programming. Develop and maintain strong communication skills with stakeholders. Ensure compliance with GCP guidelines and ICD-10 CM codes. Collaborate with cross-functional teams to achieve project goals. Perform medical coding using MedDRA, CPT, and HCPCS codes. Analyze data and prepare reports according to client requirements. Job Requirements Bachelor's or Master's degree in Life Sciences or related fields such as B.Sc./ M.Sc./ M.Pharm/ B.Pharm. Strong knowledge of clinical trial management systems and regulations. Proficiency in CPC certification, labeling assessment, and narrative writing. Experience with research and development, technica...

knowledge and handling of HPLC and GC instrument activities knowledge and handling of Wet analysis (LOD, SOR, WC and TLC) activities Testing and knowledge HPLC and GC instrument analysis Testing and knowledge of Wet analysis (LOD, SOR, WC and TLC) Computer knowledge Understanding of regulatory guidelines (ICH, USFDA, MHRA, WHO, etc.). Ability to work in a team and coordinate with cross-functional departments. Good communication skills and ability to present analytical findings.

Medblue Innovations Private Limited is looking for Regulatory Specialist to join our dynamic team and embark on a rewarding career journey We are looking for skilled Regulatory Specialists to join our team at Medblue Innovations Private Limited. The ideal candidate will have a strong background in regulatory affairs and be able to ensure compliance with relevant laws and regulations. Roles and Responsibility Develop and implement regulatory strategies to achieve business objectives. Conduct thorough reviews of regulatory documents and submissions. Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Provide expert guidance on regulatory matters to intern...

Medblue Innovations Private Limited is looking for Clinical Trial Coordinator to join our dynamic team and embark on a rewarding career journey We are looking for highly motivated and experienced Clinical Trial Coordinators to join our team at Medblue Innovations Private Limited. The ideal candidate will have a strong background in clinical trials and excellent coordination skills. Roles and Responsibility Coordinate and manage clinical trial activities, including site initiation, monitoring, and close-out visits. Develop and maintain relationships with investigators, sites, and other stakeholders to ensure successful study execution. Manage study timelines, budgets, and resources to meet pr...

We are seeking an experienced Executive to join our RD division This role will contribute to the company's success by providing leadership and strategic oversight of research initiatives, fostering innovation, and driving the development of cutting-edge products and solutions As an Executive, you will leverage your extensive knowledge of RD processes and industry trends to make strategic decisions that propel our organization forward You will collaborate with cross-functional teams, including researchers, scientists, and engineers, to identify and prioritize research directions, assess the feasibility of new ideas, and align efforts with business goals 1. Should be able to handle a reactions...

We are looking for a highly skilled and experienced Regulatory Affairs professional to join our team at Niva Bupa Health Insurance. The ideal candidate will have a strong background in regulatory affairs and excellent analytical skills. Roles and Responsibility Develop and implement regulatory strategies to achieve business objectives. Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Analyze and interpret complex regulations to identify opportunities and challenges. Prepare and submit regulatory documents to relevant authorities. Monitor and report on regulatory changes that may impact the organization. Provide training and guidance to staff on regul...

We are looking for a highly skilled and experienced ABDM-SME to join our team at Niva Bupa Health Insurance. The ideal candidate will have a strong background in sales and marketing, with excellent communication and interpersonal skills. Roles and Responsibility Develop and implement effective sales strategies to achieve business objectives. Build and maintain strong relationships with clients and stakeholders. Conduct market research and analyze industry trends to identify new business opportunities. Collaborate with cross-functional teams to drive business growth. Provide exceptional customer service and support to clients. Identify and mitigate risks associated with business operations. J...

We are looking for a highly skilled and experienced Manager to join our team at DC Mills Group. The ideal candidate will have a strong background in management and leadership, with excellent communication and problem-solving skills. Roles and Responsibility Develop and implement effective business strategies to achieve company goals. Lead and manage a team of professionals to ensure successful project execution. Analyze market trends and competitor activity to identify opportunities and threats. Build and maintain strong relationships with clients and stakeholders. Identify and mitigate risks to ensure compliance with regulatory requirements. Collaborate with cross-functional teams to drive ...

We are looking for a highly motivated and detail-oriented individual to join our team as an Internal Auditor Trainee in Manappuram Finance Ltd. The ideal candidate will have excellent analytical skills, strong communication abilities, and a keen eye for detail. Roles and Responsibility Conduct internal audits to ensure compliance with company policies and procedures. Identify and assess risks within the organization and provide recommendations for improvement. Develop and implement audit plans, test procedures, and control documents. Collaborate with management to implement corrective actions and monitor progress towards remediation. Prepare detailed reports of audit findings and present the...

Job Title: eTMF Executive Business Unit: Clinical Research Location: Mumbai At Sun Pharma, we commit to helping you “Create your own sunshine” — by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” TASKS AND RESPONSIBILITIES: Documentation and Administrative Support: Ensuring all trial-...

Introduction In this role, you'll work in one of our IBM Consulting Client Innovation Centers (Delivery Centers), where we deliver deep technical and industry expertise to a wide range of public and private sector clients around the world. Our delivery centers offer our clients locally based skills and technical expertise to drive innovation and adoption of new technology Your Role And Responsibilities Execute and Maintain Serialization Master Data Updates. Receive, review, and implement master data changes and configuration requests for Pfizer SKUs in serialization systems. Support New Product Launches and Mandate Implementations Gather required data, configure new SKUs, and ensure systems ...

Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products to meet the needs of underserved patients. They are an industry leader in providing unique, accessible, and high-quality medications. The company's patient-centric products span various markets including cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, benefiting millions of patients. Azurity Pharmaceuticals values inclusivity and is an Equal Opportunity Employer. Their success is attributed to their talented and dedicated team that focuses on improving patients" lives through science and commitment to quality. The role of Scientist ...

Description Safety & PV Coordinator (Gurgaon Office based- PV submission) Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate w...

Description Safety Specialist I Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating...

ob Overview: Prepares and negotiates and assists in the execution and retention of site agreements, confidentiality agreements, letters of indemnification and other contracts for Sponsors who contract Fortrea to perform this service. Maintains and contributes to contracts tracking and status systems and supports maintenance of paper and electronic file systems. Responsible for following SOPs including but not limited to departmental SOPs, as well as completing study-related duties in accordance with the processes set forth in the relevant process document. Primary contact with investigative site(s) during site maintenance activities with responsibility for collection of the required investig...

Roles and Responsibilities:- Collect and coordinate information and compile regulatory documentation for submission to regulatory agencies or to commercial partners, advise on the submission strategy. Preparation & compilation of dossier in CTD, ACTD, ECTD & country specific format according to guidelines of countries. Response to query/deficiency/Notice of Deficiency raised by Drug Regulatory Authority or technical representative. Coordination with Quality Control, Quality Assurance and Production department for regulatory documents. Timely compile documents for license renewals, update and re-registrations. Maintain regulatory files/database and chronologies in good order. Establish and ma...

Regulatory Affairs Associate III Job Details | Teva Pharmaceuticals We use cookies to offer you the best possible website experience. Your cookie preferences will be stored in your browser s local storage. This includes cookies necessary for the websites operation. Additionally, you can freely decide and change any time whether you accept cookies or choose to opt out of cookies to improve websites performance, as well as cookies used to display content tailored to your interests. Your experience of the site and the services we are able to offer be impacted if you do not accept all cookies. Modify Cookie Preferences Accept All Cookies Find a Career With Purpose at Teva Search by Postal Code A...

About The Role PharmacovigilanceB.Pharm / M.Pharm graduate with experience in case processing in ARGUS, experience in global submission to Health authorities. Details Location Mumbai Experience 1 - 4 years’ relevant experience in Pharmacovigilance Job Function Business Process Services Role Executive Desired Skills Pharmacovigilance | LS - Pharmacovigilance Qualifications B.Pharm / M.Pharm / BHMS / BAMS / BDS / MSc (Biotechnology, Zoology)

Job Title: Manager II – India Regulatory and business Conitnuity Business Unit: R&D1 Regulatory Affairs Job Grade G11A Location Baroda At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” Key Responsibilities: To evalua...

We are looking for skilled Regulatory Specialists to join our team at Medblue Innovations Private Limited. The ideal candidate will have a strong background in regulatory affairs and be able to ensure compliance with relevant laws and regulations. Roles and Responsibility Develop and implement regulatory strategies to achieve business objectives. Conduct thorough reviews of existing regulations and identify areas for improvement. Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Prepare and submit regulatory documents, such as applications and reports. Monitor and analyze changes in regulatory environments that could impact the company. Provide traini...