3474 Clinical Trials Jobs - Page 26

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.

Design, develop, and implement Veeva EDC clinical programming solutions for clients. Collaborate with cross-functional teams to ensure seamless integration of Veeva EDC ystems. Required Candidate profile Strong understanding of Veeva EDC principles and technologies. Experience with clinical trial data management systems. Excellent problem-solving skills and attention to detail.

Develop and implement statistical analysis plans for clinical trials. Conduct data review and quality control checks to ensure accuracy and completeness. Collaborate with cross-functional teams to design and execute studies. Required Candidate profile Strong knowledge of statistical concepts and methodologies. Experience working with clinical trial data and statistical software. Excellent communication and interpersonal 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.

Develop and implement statistical analysis plans for clinical trials. Conduct statistical reviews of case report forms, annotated CRFs, database structures, and study-related documentation. Collaborate with cross-functional teams Required Candidate profile Strong knowledge of statistical concepts, techniques, and tools. Experience in the employment firm or recruitment services industry is preferred. 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 with key stakeholders Required Candidate profile Strong understanding of clinical research principles, methodologies, and regulations. Excellent communication and interpersonal skills, with the ability to work effectively with diverse stakeholders.

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 terminology and regulations governing medical devices. Excellent analytical and problem-solving skills, with attention to detail.

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

Provide exceptional customer service to airline passengers, ensuring their comfort and satisfaction. Manage passenger complaints and concerns professionally and courteously. Coordinate with airlines and other stakeholders to resolve issues promptly. Required Candidate profile Minimum 3 years of experience in a related field, preferably in the aviation industry. Strong communication and interpersonal skills are essential. Ability to work well under pressure

Develop and implement statistical analysis plans for clinical trials. Conduct statistical reviews of case report forms, annotated CRFs, database structures, and study-related documentation. Collaborate with cross-functional teams Required Candidate profile Strong understanding of biostatistics principles and methodologies. Experience working with clinical trial data and statistical software packages. Excellent communication and interpersonal skills.

Conduct clinical trials to ensure compliance with regulatory requirements and company protocols. Collaborate with cross-functional teams to design, implement, and monitor study protocols. Provide medical guidance and support to trial participants Required Candidate profile Strong knowledge of clinical trial principles, practices, and regulations. Excellent communication and interpersonal skills are required for effective collaboration with patients, families

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.

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 and reporting. Required Candidate profile Strong knowledge of statistical concepts, methods, and techniques, with a focus on biostatistics. Experience working in the pharmaceutical industry or related field, preferably in a CRO setting.

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.

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. Collaborate with cross-functional teams Required Candidate profile Strong understanding of medical terminology and concepts. Excellent writing and communication skills. Ability to work independently and as part of a team. Proficient in using content management

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 Minimum 5 years of experience in medical writing or a related field. Strong understanding of medical terminology, anatomy, and physiology. Excellent writing, editing, and communication skills.

Design, develop, and implement clinical trial data management systems using CDMS expertise. Collaborate with cross-functional teams to ensure seamless integration of clinical trial data into the overall study design. Required Candidate profile Strong understanding of clinical trial data management principles and CDMS expertise. Proficiency in SAS programming language with experience in developing complex statistical analysis plans.

Conduct thorough medical device safety assessments and evaluations. Develop and implement effective safety protocols and procedures. Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Analyze data and trends Required Candidate profile Strong knowledge of medical devices and their safety regulations. Excellent analytical and problem-solving skills. Ability to work effectively in a fast-paced environment. Strong communication

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.

Analyze clinical data to identify trends and patterns, providing insights to stakeholders. Develop and maintain databases and systems for tracking and managing clinical data. Collaborate with cross-functional teams to ensure data quality Required Candidate profile Strong analytical and problem-solving skills, with attention to detail and the ability to interpret complex data. Excellent communication and interpersonal skills, enabling effective collaboration

Conduct thorough analysis of clinical trial data to identify potential safety concerns. Develop and implement effective safety protocols to mitigate risks associated with medical devices. Collaborate with cross-functional teams Required Candidate profile Strong understanding of clinical trials, medical devices, and regulatory requirements. Excellent analytical and problem-solving skills. Ability to work effectively in a fast-paced environment.