2887 Regulatory Requirements Jobs - Page 9

Publish and maintain regulatory documents, ensuring accuracy and compliance with industry standards.Collaborate with cross-functional teams to ensure timely submission of regulatory documents. Required Candidate profile Strong knowledge of regulatory requirements and guidelines. Excellent communication and interpersonal skills. Ability to work independently and as part of a team.

Conduct thorough medical reviews of device-related documents to ensure compliance with regulatory requirements.Collaborate with cross-functional teams to identify and resolve issues related to device safety and efficacy. Required Candidate profile Strong understanding of medical devices and equipment, including their design, development, and testing. Familiarity with relevant software and tools used in medical device development and review.

Develop and implement statistical analysis plans for clinical trials, ensuring compliance with regulatory requirements.Collaborate with cross-functional teams to design and conduct statistical studies, including data management Required Candidate profile Strong understanding of statistical concepts, including hypothesis testing, confidence intervals, and regression analysis. Experience working with clinical trial data,data management, cleaning.

Manage and oversee the development, implementation, and maintenance of clinical data management systems.Collaborate with cross-functional teams to ensure accurate and timely delivery of clinical data. Required Candidate profile Strong knowledge of Veeva EDC system and its applications in clinical trials. Experience in managing clinical data in a fast-paced environment. Excellent analytical and problem-solving

Manage and oversee the development, implementation, and maintenance of clinical data management systems.Ensure compliance with regulatory requirements and industry standards for clinical data management Required Candidate profile Strong knowledge of Veeva EDC and clinical data management principles. Excellent analytical and problem-solving skills with attention to detail. Ability to work effectively in a team environment

Develop high-quality regulatory documents, including clinical trial applications and marketing authorizations.Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Required Candidate profile Minimum 2 years of experience in regulatory medical writing or a related field. Strong knowledge of regulatory requirements, including FDA, EMA, and ICH guidelines.

Develop high-quality regulatory documents, including clinical trial applications and marketing authorizations.Collaborate with cross-functional teams to ensure compliance with regulatory requirements Required Candidate profile Minimum 2 years of experience in regulatory writing, preferably in the pharmaceutical or healthcare industry. Strong understanding of regulatory requirements, including FDA, EMA, and ICH guidelines.

Publish regulatory documents accurately and efficiently.Ensure compliance with industry standards and regulations.Collaborate with cross-functional teams to meet business objectives. Required Candidate profile Strong understanding of regulatory requirements and guidelines. Excellent communication and interpersonal skills. Ability to work independently and as part of a team.Strong analytical skill

Manage and maintain accurate clinical data records, ensuring compliance with regulatory requirements.Perform data reconciliation tasks to ensure accuracy and consistency across systems.Collaborate with cross-functional teams 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 skills

Publish regulatory documents accurately and efficiently.Ensure compliance with industry standards and regulations.Collaborate with cross-functional teams to meet business objectives Required Candidate profile Strong understanding of regulatory requirements and guidelines. Excellent communication and interpersonal skills. Ability to work independently and as part of a team.

Develop high-quality regulatory documents, including clinical trial applications and marketing authorizations.Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Required Candidate profile Minimum 2 years of experience in regulatory writing, preferably in the pharmaceutical or biotechnology industry. Strong knowledge of regulatory requirements, including FDA, EMA, and ICH guidelines.

Manage and analyze revenue data to optimize business performance.Develop and implement effective revenue strategies to drive growth.Collaborate with cross-functional teams to achieve business objectives Required Candidate profile Strong knowledge of revenue accounting principles and practices. Excellent analytical and problem-solving skills. Ability to work effectively in a fast-paced environment.

Manage and maintain accurate clinical data records, ensuring compliance with regulatory requirements.Perform data reconciliation tasks to ensure accuracy and consistency across systems.Collaborate with cross-functional teams Required Candidate profile Strong understanding of clinical data management principles and practices. Proficiency in data analysis and problem-solving skills with attention to detail.

Publish regulatory documents accurately and efficiently.Ensure compliance with industry standards and regulations.Collaborate with cross-functional teams to meet business objectives Required Candidate profile Strong understanding of regulatory requirements and guidelines. Excellent communication and interpersonal skills. Ability to work independently and as part of a team.

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About Us Tsaaro Consulting's prime focus is on Data Privacy and Security Our team of specialist Data Privacy Consultants, Information Security Consultants, and penetration testers help and advise our Clients to make running a secure business easier with high efficiency Everything We do is tailored to the individual, and organisational requirements, aligned with their budget and resource challenges We take a pragmatic, risk-based approach to provide our clients with real-world, workable advice, guidance, and support That helps them to deal with a wide range of security and privacy-related challenges At Tsaaro, we adopt a pragmatic, risk-based strategy to deliver practical and effective advice...

Develop high-quality regulatory documents, including clinical trial applications and marketing authorizations. Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Required Candidate profile Minimum 2 years of experience in regulatory writing, preferably in the pharmaceutical or biotechnology industry. Strong understanding of regulatory requirements,

Publish regulatory documents accurately and efficiently.Ensure compliance with industry standards and regulations.Collaborate with cross-functional teams to meet business objectives Required Candidate profile Strong understanding of regulatory requirements and guidelines. Excellent communication and interpersonal skills. Ability to work independently and as part of a team

Manage and analyze airline cargo revenue data to identify trends and areas for improvement. Develop and implement effective revenue management strategies to optimize cargo capacity and rates. Required Candidate profile Strong understanding of airline cargo operations, including pricing, capacity, and route planning. Excellent analytical and problem-solving skills, with the ability to interpret complex data sets.

Manage and analyze cargo revenue data to identify trends and areas for improvement. Develop and implement effective revenue accounting strategies to optimize business growth. Required Candidate profile Strong understanding of cargo revenue accounting principles and practices. Proficiency in analyzing complex data sets and identifying key trends and patterns.

Develop and implement statistical analysis plans for clinical trials, ensuring compliance with regulatory requirements. Collaborate with cross-functional teams to design and conduct statistical studies. Required Candidate profile Ability to work independently and as part of a team, demonstrating strong leadership and mentoring skills. Proficiency in statistical software packages, such as SAS or R,

Manage and analyze airline cargo revenue data to identify trends and areas for improvement. Develop and implement effective revenue management strategies to optimize cargo operations. Required Candidate profile Strong understanding of revenue accounting principles and practices in the airline industry. Experience working with cargo operations, preferably in an airline setting.

Manage and coordinate international shipping operations for timely and efficient delivery. Develop and implement effective shipping strategies to meet business objectives. Required Candidate profile Minimum 2 years of experience in international shipping operations or a related field. Strong knowledge of shipping regulations, laws, and practices.

Manage and analyze airline cargo revenue data to identify trends and areas for improvement. Develop and implement effective revenue management strategies to optimize cargo operations. Required Candidate profile Strong understanding of revenue accounting principles and practices in the airline industry. Experience working with cargo operations, including shipment tracking and billing.

Develop and implement statistical analysis plans for clinical trials. Conduct statistical reviews of case report forms, annotated CRFs, database structures, and study-related documentation. Required Candidate profile Strong knowledge of statistical concepts, including regression, time series, mixed effects, and survival analysis. Experience with statistical software packages such as SAS, R, or Python.