731 Ich-Gcp Guidelines Jobs - Page 4

Manage and oversee clinical 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 data management principles and practices. Experience with data management systems and software applications. Excellent analytical and problem-solving skills.

Coordinate and manage shipping operations, including arranging transportation and logistics. Develop and maintain relationships with clients, suppliers, and other stakeholders. Prepare and review shipping documents. Required Candidate profile Strong knowledge of shipping regulations, laws, and practices. Excellent communication, negotiation, and problem-solving skills. Ability to work in a fast-paced environment and meet deadlines.

Manage and oversee clinical data management activities, ensuring compliance with regulatory requirements. Develop and implement effective data management plans to ensure data quality and integrity. Collaborate with cross-functional teams Required Candidate profile Strong knowledge of clinical data management principles and practices. Experience with data management systems and software applications. Excellent analytical and problem-solving skills

Manage and oversee clinical data management activities, ensuring compliance with regulatory requirements. Develop and implement effective data management plans to ensure data quality and integrity. Collaborate with cross-functional teams Required Candidate profile Strong knowledge of clinical data management principles and practices. Experience with data management systems and software applications. Excellent analytical and problem-solving skills

Conduct thorough reviews of clinical data to ensure accuracy and compliance with regulatory requirements. Collaborate with cross-functional teams to identify and resolve data discrepancies. Develop and implement effective data management strategies Required Candidate profile Strong understanding of clinical data review principles and practices. Excellent analytical and problem-solving skills with attention to detail. Effective communication and interpersonal skills

Publish regulatory submissions to relevant authorities, ensuring compliance with required standards and regulations. Coordinate with cross-functional teams to ensure timely submission of regulatory documents. Review and edit regulatory documents 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 thorough medical reviews and assessments to ensure compliance with regulatory requirements. Collaborate with cross-functional teams to develop and implement clinical development strategies. Provide expert guidance on medical aspects Required Candidate profile Strong understanding of clinical development principles and practices. Excellent analytical and problem-solving skills, with attention to detail. Effective communication and interpersonal skills

Coordinate regulatory submissions and ensure compliance with relevant laws and regulations. Prepare and review regulatory documents, including applications and reports. Collaborate with cross-functional teams to meet regulatory requirements. Required Candidate profile Strong knowledge of employment firms and recruitment services. Excellent communication and coordination skills. Ability to work effectively in a fast-paced environment. Strong analytical skills.

Monitor medical enquiries and respond to queries from clients and stakeholders. Provide excellent customer service and ensure timely resolution of medical inquiries. Collaborate with internal teams to resolve complex medical issues. Required Candidate profile Strong knowledge of medical terminology and concepts. Excellent communication and interpersonal skills. Ability to work effectively in a fast-paced environment and prioritize tasks.

Manage and oversee clinical data management activities, ensuring compliance with regulatory requirements. Develop and implement effective data management plans to ensure data quality and integrity. Collaborate with cross-functional teams to identify Required Candidate profile Strong knowledge of clinical data management principles and practices. Experience with data management systems and software applications. Excellent analytical and problem-solving skills

Design, develop, and implement clinical SAS programs for data management and analysis. Develop and maintain complex SQL databases for data storage and retrieval. Collaborate with cross-functional teams to identify business requirements Required Candidate profile Strong proficiency in SAS programming language, including Base SAS, Enterprise Guide, and Macros. Experience with SQL database management systems, including design, development, and maintenance.

Develop high-quality aggregate reports on medical data, including patient safety and efficacy.Conduct thorough analysis of medical records to identify trends and patterns.Collaborate with cross-functional teams to ensure accurate Required Candidate profile Minimum 2 years of experience in medical writing, preferably in Pharmacovigilance. Strong knowledge of medical terminology, regulations, and industry standards. Excellent writing, communication,

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. Excellent communication and coordination skills. Ability to work independently and as part of a team.

We seek a highly motivated and detail-oriented Clinical Trial Associate (CTA) to join our clinical research team. The CTA will support the planning, execution, and management of clinical trials, ensuring compliance with regulatory guidelines and company protocols. This role requires strong organizational skills, excellent communication, and the ability to collaborate effectively with cross-functional teams. Key Responsibilities: Assist in the coordination and management of clinical trials from initiation to completion. Maintain and update trial documentation, including investigator brochures, protocols, and informed consent forms. Ensure compliance with Good Clinical Practice (GCP), regulato...

Job Purpose Compliance advisory role involves providing guidance and support to organisations on compliance matters. Compliance advisors stay up to date with legal and regulatory developments, assess their impact on the organisation, and provide recommendations to ensure compliance. Duties and Responsibilities Providing advice on all lending & deposit products to businesses Review policies/product /process notes and approve after verifying adherence to regulatory requirements. Review product journey / documentation and confirm before Go-Live. Advising management on the companys compliance with laws and regulations through detailed reports Researching industry compliance regulations and polic...

We are looking for a skilled Medical Writer with 5-10 years of experience to join our team in Hyderabad. The ideal candidate will have excellent writing and editing skills, with the ability to create clear, concise, and engaging content. Roles and Responsibility Develop high-quality medical content, including articles, blogs, and other written materials. Conduct research and analyze complex scientific concepts to create accurate and informative content. Collaborate with cross-functional teams to ensure consistency and quality of content. Edit and proofread content for clarity, grammar, and punctuation. Stay up-to-date with industry trends and developments in medical science and technology. P...

We are looking for a skilled finance professional with 10-18 years of experience to join our team as an Associate Director of Finance in the Hotels & Restaurants industry. Roles and Responsibility Oversee financial planning, budgeting, and forecasting to drive business growth. Develop and implement financial strategies to optimize profitability and minimize losses. Lead financial analysis and reporting to inform business decisions. Manage financial risk and ensure compliance with regulatory requirements. Collaborate with cross-functional teams to achieve business objectives. Provide financial guidance and support to senior management. Job Requirements Strong background in finance, accounting...

We are looking for a skilled Manager Admin to join our team in the hospitality industry. The ideal candidate will have 3-7 years of experience and be based in Saaki Argus & Averil Consulting. Roles and Responsibility Manage administrative tasks with precision and attention to detail. Coordinate with various departments to ensure smooth operations. Develop and implement effective administrative processes and procedures. Supervise and guide junior staff members. Maintain accurate records and reports. Ensure compliance with company policies and regulations. Job Requirements Proven experience in administration or a related field. Strong knowledge of administrative principles and practices. Excel...

- NISM 8 (Equity Derivative) must - Strong Understanding of stock market and Financial regulations. - Excellent Analytical and decision making skills - Ability to work under pressure and quick decisions. - MF certification is added advantage

We are seeking a highly organized and detail-oriented Clinical Trial Coordinator (Fresher) to join our dynamic clinical research team. In this role, you will play a crucial part in ensuring the successful execution of our clinical trials from start to finish. You will collaborate with a multidisciplinary team of researchers, investigators, and study personnel to coordinate all aspects of clinical trial operations. Key Responsibilities: Study Coordination: Coordinate the day-to-day activities of assigned clinical trials, ensuring adherence to protocols, timelines, and regulatory requirements. Site Management: Assist in site selection, initiation, monitoring, and close-out activities. Document...

Position Summary: The Executive Regulatory Affairs (Biosimilars) will be responsible for the preparation, review, and submission of high-quality CMC documentation to support regulatory filings in the US, Europe, and other global markets. The role involves cross-functional collaboration, drafting of eCTD modules, and ensuring compliance with international regulatory requirements for biosimilar products. Role & responsibilities Review and finalize CMC (Chemistry, Manufacturing, and Controls) documents for US (FDA) and European (EMA) regulatory submissions. Draft, compile, and review eCTD sections , ensuring compliance with current regulatory and technical standards. Author and review key regul...

About The Role Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services Associate Qualifications: Bachelor of Pharmacy/Bachelor in Physiotherapy/Bachelor Degree in Life Sciences Years of Experience: 1 to 3 years Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on ...

About The Role Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services New Associate Qualifications: Bachelor of Pharmacy/Bachelor Degree in Life Sciences Years of Experience: 0 to 1 years Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technol...

Looking to onboard a skilled Driver with 2-5 years of experience in the hospitality industry, preferably in hotels and restaurants. The ideal candidate will have excellent driving skills and be able to work efficiently in a fast-paced environment. Roles and Responsibility Drive company vehicles safely and professionally. Ensure timely delivery of passengers and cargo. Maintain accurate records of trips and routes. Collaborate with other drivers to achieve transportation goals. Adhere to traffic laws and regulations. Provide exceptional customer service to passengers. Job Requirements Proven experience as a driver in the hospitality industry. Strong knowledge of traffic laws and regulations. ...

About The Role Skill required: KYC Screening - Know Your Customer (KYC) Designation: Regulatory Compliance New Associate Qualifications: Any Graduation Years of Experience: 0 to 1 years Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries...