603 Case Processing Jobs - Page 3

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.

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

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.

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

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 technologies. Excellent communication and interpersonal skills.

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 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.

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.

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.

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.

Collaborate with cross-functional teams to design and implement clinical research studies. Provide medical expertise and guidance on study protocols, case report forms, and informed consent documents. Required Candidate profile Strong knowledge of clinical research principles, regulations, and guidelines. Excellent communication and interpersonal skills. Ability to work effectively in a team environment.

Manage and oversee the collection, management, and analysis of clinical study data. Develop and implement effective data management plans to ensure compliance with regulatory requirements. Required Candidate profile Strong understanding of clinical trial protocols and regulations. Experience with data management systems and software applications. Excellent analytical and problem-solving skills.

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 medical documentation. Required Candidate profile Strong understanding of medical terminology and regulations governing the device industry. Excellent analytical and problem-solving skills with attention to detail.

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 from various sources, including electronic health records and laboratory results.

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.

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

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 with key stakeholders 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.

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 with key stakeholders 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.