5955 Pharmaceutical Jobs - Page 49

Manage and oversee clinical study data management activities, ensuring compliance with regulatory requirements.Develop and implement effective data management plans to ensure data quality and integrity. Required Candidate profile Strong knowledge of clinical trial conduct, including GCP guidelines and regulatory requirements.Experience with data management systems, such as electronic data capture and database management.

Conduct thorough medical device safety assessments and evaluations.Develop and implement effective safety protocols and procedures.Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Required Candidate profile Strong knowledge of medical devices and their safety regulations.Excellent analytical and problem-solving skills.Ability to work effectively in a team environment.

Manage and maintain accurate clinical data records, ensuring compliance with regulatory requirements.Perform data reconciliation tasks to identify and resolve discrepancies in clinical trial data. Required Candidate profile Strong understanding of clinical data management principles and practices.Proficiency in data analysis and problem-solving skills with attention to detail.Excellent communication and collaboration

Develop and implement project plans, resource allocation, and timelines to ensure successful project execution.Collaborate with cross-functional teams to identify and mitigate risks, ensuring compliance with regulatory requirements. Required Candidate profile Strong understanding of pharmaceutical projects, including regulations, standards, and best practices.Excellent planning, organizational, and problem-solving skills,

Required Skills and Qualifications : - Looking for a Business Analyst in Life Sciences and Heathcare domain. - Need to have Clinical domain background. - At least 5 years of experience in a business analysis role with a focus on clinical data management within the pharmaceutical, biotechnology, or healthcare industry. - Deep understanding of clinical trial processes, data management principles, and regulatory compliance requirements. - Proficient in the use of data management software and tools, with a strong emphasis on EDC systems, Data Management Workbench type systems, SQL. - Demonstrated ability to perform data analysis and present findings in a clear and concise manner. - Excellent pro...

SUMMARY Retail Associate / Store Helper / Merchandiser / Cashier / Store Assistant Job Summary: We are seeking highly motivated and customer-focused Retail Associates to join our team. As a Retail Associate, you will play a vital role in ensuring the smooth operation of our store, providing exceptional customer service, and maintaining a clean and organized store environment. This is an excellent opportunity for fresher or experienced candidates to kick-start their career in retail and contribute to the success of our team. Responsibilities: Assist in day-to-day store operations, including stocking, billing, display arrangement, and housekeeping. Provide excellent customer service, handle pr...

Key Responsibilities Develop, design, and maintain interactive Power BI dashboards and reports to support omnichannel and digital analytics initiatives. Partner with business stakeholders to understand KPIs, campaign performance metrics, and reporting needs. Work with large datasets from multiple sources (CRM, digital campaigns, email, social, etc.) to generate actionable insights. Build data models, define relationships, and optimize queries for performance and scalability. Collaborate with Data Engineers and Data Scientists to align reporting layers with backend data pipelines. Provide ad hoc analysis and visualizations to support marketing effectiveness and ROI measurement. Ensure data qu...

8 years experiences for RA role in medical device and or pharmaceutical industry.Good understanding for regulations and policies issued by India, US FDA and EU, and ability to interpret international regulatory requirements. Required Candidate profile Desired Skills:RA role in medical device, US FDA and EU. Bachelor degree in Medical, Mechanical, Electric Life Science or other healthcare related majors.

Procurement Operations: Source and procure raw materials (APIs, excipients), packaging materials, and other pharma-related items. Evaluate purchase requisitions and coordinate with internal departments (production, QA/QC, R&D) to ensure timely procurement. Issue purchase orders (POs) and track their status until delivery and GRN. Vendor Management: Identify, evaluate, and develop new suppliers and maintain strong supplier relationships. Negotiate prices, payment terms, delivery schedules, and contracts. Monitor vendor performance based on quality, cost, delivery, and service. Inventory & Cost Control: Coordinate with the inventory team to maintain optimum stock levels. Analyze and control pr...

About The Role Skill required: Pharmacovigilance Operations - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services Associate Qualifications: Bachelor of Pharmacy/Master of Pharmacy Years of Experience: 1 to 3 years What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vision to li...

Job Summary We are seeking a dynamic and experienced Production Shift Chemist in Active Pharmaceutical Ingredient (API) to support the development of robust and cost effective API's by executing scale up batches for all new and existing APIs at GMP Kilo Lab. Roles & Responsibilities You will be responsible for Equipment Operations of Reactors (GL, SS & All Glass), Mobile Receivers & tanks, ANFD, PNF & VTD, Isolators (Reactor Charging, ANFD Discharge, Dispensing/packing, sifter & multimill), Air jet mill, Multimill, Blender & Sifter, Spray dryer, TCU, Vacuum Pumps, AODD Pumps, centrifugal pumps & peristatic pumps, VNS sealing machine, RLAF & dispensing booth, Refrigerators and Deep freezers e...

About The Role Skill required: KYC Screening - Know Your Customer (KYC) Designation: Regulatory Compliance New Associate Qualifications: BCom Years of Experience: 0 to 1 years What would you do? Help clients transform their compliance function from reactive to proactive through an intelligent compliance operating model – powered by data, intelligent technologies and talentLooking for someone with KYC experience along with ECDD/OCDD knowledgeBusiness and regulatory requirements, governance, operating model, process and system controls to verify the identity, suitability, and risks involved with onboarding and/or maintaining a business / customer relationship. This includes driving customer id...

About The Role Skill required: KYC Screening - Know Your Customer (KYC) Designation: Regulatory Compliance Analyst Qualifications: Any Graduation Years of Experience: 3 to 5 years What would you do? Help clients transform their compliance function from reactive to proactive through an intelligent compliance operating model – powered by data, intelligent technologies and talentLooking for someone with AML and Fraud mgmt experience.Understand & implement laws, and regulations designed to stop the practice of generating income through illegal actions during transfer of funds. Anti Money Laundering law covers limited number of transactions and criminal behaviors to prevent terrorist financing an...

Accurately code medical records using relevant codes and guidelines.Ensure compliance with regulatory requirements and industry standards.Collaborate with healthcare professionals to clarify coding discrepancies. Required Candidate profile Strong knowledge of medical terminology and coding principles. Experience with electronic health records (EHR) systems. Familiarity with coding software and tools.

Develop and implement project plans to ensure timely completion of pharmaceutical projects.Coordinate with cross-functional teams, including production, quality control, and regulatory affairs. Required Candidate profile Strong understanding of pharmaceutical project planning principles and practices. Excellent communication, leadership skills. Ability to work in a fast-paced environment with multiple priorities

Publish regulatory submissions to relevant authorities, ensuring compliance with required standards.Coordinate with cross-functional teams to ensure timely submission of regulatory documents. Required Candidate profile Strong understanding of regulatory requirements and guidelines governing submissions. Excellent publishing skills, including attention to detail and ability to meet deadlines.

Collaborate with internal stakeholders to resolve issues related to regulatory submissions.Stay updated with changes in regulatory requirements and implement necessary updates to publishing processes. Required Candidate profile Experience in regulatory submissions publishing, preferably in the employment or recruitment industry. Strong understanding of regulatory requirements and guidelines governing submissions.

Conduct quality control checks on data accuracy and completeness.Provide training and support to staff on data management best practices.Ensure timely delivery of high-quality data products to stakeholders. Required Candidate profile Strong understanding of clinical trial operations and regulations. Experience with data management systems and software applications. Excellent analytical and problem-solving skills

Conduct thorough analysis of clinical trial data to identify potential safety risks and trends.Develop and implement effective safety protocols and procedures to mitigate identified risks.Monitor and report adverse events Required Candidate profile Strong understanding of clinical safety principles, regulations, and standards (e.g., GCP). Experience working with medical devices or pharmaceuticals is preferred.

Manage and publish regulatory submissions to relevant authorities.Ensure compliance with regulatory requirements and guidelines.Coordinate with internal teams to gather necessary information for submissions. Required Candidate profile Strong understanding of regulatory requirements and guidelines. Excellent communication and coordination skills. Ability to work independently and as part of a team.

Design, develop, and maintain clinical databases using R/SQL.Collaborate with cross-functional teams to ensure data quality and integrity.Develop and implement data validation and verification processes. Required Candidate profile Strong knowledge of R/SQL programming languages. Experience working with clinical data management systems. Understanding of database design principles and data modeling techniques.

Develop high-quality medical content for various platforms, including reports and presentations.Conduct research and analyze data to create accurate and informative medical documents. Required Candidate profile Minimum 2 years of experience in medical writing or a related field. Strong understanding of medical terminology and concepts. Excellent writing, editing, and communication skills.

Develop high-quality medical content for various platforms, including reports and presentations.Conduct thorough research on medical topics and stay updated with the latest developments.Collaborate with cross-functional teams Required Candidate profile Strong understanding of medical terminology and concepts. Excellent writing and communication skills. Ability to work independently and as part of a team.

Develop high-quality written materials for various medical publications, including articles, blogs, and social media posts.Conduct research on medical topics and stay updated with the latest developments in the field. Required Candidate profile Minimum 3 years of experience in medical writing or a related field. Strong understanding of medical terminology, anatomy, and physiology. Excellent writing, editing, and communication skills.

Manage and oversee clinical study data management activities, ensuring compliance with regulatory requirements.Develop and implement effective data management plans to ensure data quality and integrity. Required Candidate profile Strong knowledge of clinical trial conduct, including GCP guidelines and regulatory requirements. Experience with data management systems, such as electronic data capture and case report forms.