683 Meddra Jobs - Page 3

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 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 Strong understanding of medical terminology and concepts. Excellent communication skills. Ability to work independently and as part of a team. Proficient in using computer software applications

Coordinate and prepare regulatory submissions, including applications, reports, and other documents.Ensure compliance with relevant laws, regulations, and industry standards.Develop and maintain relationships Required Candidate profile Strong knowledge of regulatory submissions, compliance, and industry standards. Excellent communication and interpersonal skills. Ability to work independently and as part of a team.

Monitor medical enquiries and respond to queries from clients and stakeholders.Coordinate with healthcare professionals to resolve patient inquiries and concerns.Develop and maintain relationships with key stakeholders Required Candidate profile Strong communication and interpersonal skills are essential for effective collaboration with healthcare professionals. Ability to work in a fast-paced environment and prioritize tasks effectively.

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.

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.

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.

Develop high-quality written materials for various medical publications, including articles, reports, and presentations.Conduct research and analyze data to create accurate and informative content.Collaborate with cross-functional teams Required Candidate profile Minimum 2 years of experience in medical writing or a related field. Strong understanding 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.Develop and maintain relationships Required Candidate profile Strong understanding of clinical research principles, regulations, and guidelines. Excellent communication and interpersonal skills, with the ability to work effectively with diverse stakeholders

Develop high-quality aggregate reports related to pharmacovigilance. Conduct thorough research and analysis to identify trends and patterns in medical data. Collaborate with cross-functional teams to ensure timely delivery of reports. Required Candidate profile Minimum 2 years of experience in medical writing, preferably in pharmacovigilance or aggregate reporting. Strong knowledge of pharmacovigilance principles and regulations.

Develop high-quality aggregate reports related to pharmacovigilance. Conduct thorough research and analysis to identify trends and patterns in medical data. Required Candidate profile Minimum 2 years of experience in medical writing, preferably in pharmacovigilance. Strong knowledge of aggregate reporting principles and practices.

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 regulations and guidelines, including GCP and ICH. Experience with data management systems, such as Oracle or SQL.

Develop high-quality written content 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 Collaborate with cross-functional teams to create engaging and informative content. Edit and proofread content for accuracy, clarity, and consistency.

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. Required Candidate profile Collaborate with cross-functional teams to ensure accurate and consistent messaging. Create engaging and informative content that meets the needs of diverse audiences.

Conduct thorough medical reviews and assessments to ensure compliance with regulatory requirements. Collaborate with cross-functional teams to develop and implement clinical development strategies. Required Candidate profile Strong understanding of clinical development principles, regulations, and guidelines.Excellent communication and interpersonal skills, with the ability to work effectively with diverse stakeholders.

Conduct thorough medical reviews of patient records, including diagnoses, treatments, and test results. Analyze data to identify trends and patterns, providing insights that inform medical decisions. Required Candidate profile Strong understanding of medical terminology, regulations, and standards. Excellent analytical and problem-solving skills, with attention to detail.

Develop high-quality aggregate reports on medical data, including patient safety and efficacy. Conduct thorough analysis of medical records to identify trends and patterns. Required Candidate profile Minimum 2 years of experience in medical writing, preferably in Pharmacovigilance. Strong knowledge of medical terminology, anatomy, and physiology.

Monitor clinical development projects to ensure compliance with regulatory requirements. Collaborate with cross-functional teams to identify and mitigate risks. Develop and implement quality control processes to maintain high standards. Required Candidate profile Strong knowledge of clinical development regulations and guidelines. Excellent communication and interpersonal skills. Ability to work independently and as part of a team.

Conduct thorough medical reviews and assessments to ensure compliance with regulatory requirements. Collaborate with cross-functional teams to develop and implement clinical development strategies. Required Candidate profile Strong understanding of clinical development principles and practices. Excellent analytical and problem-solving skills, with attention to detail.

Collaborate with cross-functional teams to ensure seamless clinical development processes. Develop and implement effective monitoring strategies to enhance patient outcomes. Conduct thorough reviews of medical records and reports. Required Candidate profile Strong understanding of clinical development principles and practices. Excellent analytical and problem-solving skills with attention to detail.

Develop and implement effective aggregate reporting strategies to meet business objectives. Analyze complex data sets to identify trends and patterns, providing insights to stakeholders. Required Candidate profile Minimum 2 years of experience in aggregate reporting or a related field. Strong understanding of employment firms and recruitment services. Excellent analytical and problem-solving skills.

Coordinate and conduct clinical trials, ensuring compliance with regulatory requirements. Collaborate with cross-functional teams to develop and implement study protocols. Required Candidate profile Strong knowledge of clinical trial regulations, GCP guidelines, and ICH guidelines. Excellent communication and interpersonal skills, with the ability to work effectively with diverse stakeholders.