6754 Clinical Research Jobs - Page 50

Analyze and interpret complex clinical trial data to inform business decisions.Develop and maintain databases, spreadsheets, and reports using SAS and Veeva.Collaborate with cross-functional teams Required Candidate profile Strong proficiency in SAS programming language and Veeva software. Experience working with large datasets and performing complex data analysis tasks. Excellent problem-solving skills

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.

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 data management. Excellent analytical and problem-solving skills with attention to detail.

Conduct thorough medical reviews of patient records, including diagnoses, treatments, and test results.Analyze data from various sources, such as electronic health records and laboratory reports, to identify trends Required Candidate profile Strong knowledge of medical terminology, anatomy, and physiology. Excellent analytical and problem-solving skills, with attention to detail and the ability to interpret complex data.

Design, develop, and implement clinical trial data management systems using SAS.Develop and maintain databases for clinical trial data, ensuring data quality and integrity.Collaborate with cross-functional teams Required Candidate profile Strong knowledge of SAS programming language, including Base SAS and Enterprise Guide. Experience with clinical trial data management, statistical analysis, and database development.

Develop high-quality medical documents, including reports, articles, and other written materials.Review and edit medical documents for accuracy, clarity, and consistency.Collaborate with cross-functional teams Required Candidate profile Minimum 3 years of experience in medical writing or reviewing. Strong knowledge of medical terminology, anatomy, and physiology. Excellent writing, editing, and communication skills.

Collaborate with cross-functional teams to develop and implement clinical research studies.Provide medical expertise and guidance on study design, methodology, and statistical analysis. Required Candidate profile Strong understanding of clinical research principles, regulations, and guidelines. Excellent communication and interpersonal skills. Ability to work effectively in a team environment.

Monitor medical enquiries from patients and respond to their queries professionally.Provide excellent customer service to patients and resolve their concerns promptly.Collaborate with healthcare professionals to ensure seamless patient care. Required Candidate profile Minimum 3 years of experience in a related field, preferably in healthcare or recruitment. Strong knowledge of medical terminology and procedures. Excellent communication and interpersonal skills.

Monitor medical enquiries and respond to client queries professionally. Coordinate with clients to understand their requirements and provide suitable candidates. Conduct thorough interviews and assessments to ensure the best fit for each role. Required Candidate profile Minimum 3 years of experience in a related field, preferably in recruitment or healthcare. Strong knowledge of medical terminology and procedures. Excellent communication and interpersonal skills.

Manage and maintain accurate clinical data records.Perform data reconciliation tasks to ensure accuracy and completeness.Collaborate with cross-functional teams to resolve data discrepancies Required Candidate profile Strong understanding of clinical data management principles. Proficient in data analysis and reporting tools. Excellent communication and problem-solving skills.

Design, develop, and maintain complex statistical analysis systems using SAS.Collaborate with cross-functional teams to ensure timely delivery of high-quality results.Develop and implement data validation and quality control processes Required Candidate profile Strong knowledge of SAS programming language and its applications in clinical trial data management. Experience with SQL database management systems and data analysis tools.

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

Develop and implement regulatory compliance programs to ensure adherence to industry standards.Publish regulatory documents, such as reports and updates, on time and accurately. Required Candidate profile Strong knowledge of regulatory compliance principles and practices. Excellent writing and publishing skills, with attention to detail and accuracy.

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

Conduct thorough reviews of ECR data to ensure accuracy and compliance with company standards.Identify and report any discrepancies or errors in the ECR system.Collaborate with cross-functional teams to resolve issues Required Candidate profile Strong understanding of ECR systems and data review principles. Excellent analytical and problem-solving skills with attention to detail. Ability to work effectively in a fast-paced 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 writing, preferably in the pharmaceutical or biotechnology industry. Strong knowledge of regulatory requirements, including FDA, EMA, and ICH guidelines.

Analyze and interpret complex clinical trial data to inform business decisions.Develop and maintain databases, spreadsheets, and reports using SAS and Veeva.Collaborate with cross-functional teams to design Required Candidate profile Strong knowledge of SAS programming language and Veeva software. Experience working with large datasets and performing complex data analysis tasks. Excellent problem-solving skills

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.

Work Flexibility: Onsite Who we want: Hard-working winners. Confident, competitive and results-oriented professionals who create a track record of success. Dedicated achievers. People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations. Effective communicators. People who can interpret information clearly and accurately to concisely communicate results and recommendations to stakeholders. Collaborative partners. People who build and leverage cross-functional relationships to bring together ideas, information, use cases, and industry analyses to develop best practices. What you will do: Relationship management ...

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...

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,