3474 Clinical Trials Jobs - Page 23

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 clinical data systems using R/SQL.Collaborate with cross-functional teams to ensure data quality and integrity.Develop and implement data validation and verification processes. Required Candidate profile Strong knowledge of R/SQL programming languages. Experience working with clinical data systems and databases. Understanding of data modeling and data warehousing concepts.

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.

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

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.

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 ...

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,

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.

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.

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.

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. 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.

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 and maintain SAS programs for clinical trial data management, including data cleaning, transformation, and visualization. Collaborate with cross-functional teams to ensure timely delivery of high-quality deliverables. Required Candidate profile Strong knowledge of SAS programming language, including Base SAS, Enterprise Guide, and Macros. Experience with clinical trial data management systems, such as CDISC or Oracle Argus Safety.

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.

Conduct clinical trials to ensure compliance with regulatory requirements and company protocols. Collaborate with cross-functional teams, including data management, biostatistics, and medical writing. Required Candidate profile Develop and implement study-specific procedures and protocols. Monitor and report adverse events during clinical trials. Ensure timely completion of studies within budget and quality standards.

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.

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

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.

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,

Develop and implement statistical analysis plans for clinical trials. Conduct statistical programming activities, including data management, reporting, and visualization. Required Candidate profile Strong knowledge of biostatistics and statistical programming principles. Excellent analytical, problem-solving, and communication skills. Ability to work independently and as part of a team.

Design, develop, and implement electronic data capture systems for various clients. Collaborate with cross-functional teams to identify business requirements and develop solutions. Required Candidate profile Strong understanding of EDC principles and methodologies. Proficiency in programming languages such as Java or Python. Experience with EDC tools and technologies is desirable.

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.