581 Clinical Operations Jobs

As a Senior Clinical Operations Specialist (Senior CTA) at Syneos Health in Athens, you will play a crucial role in ensuring compliance with Corporate and Clinical Operations Policies, Standard Operating Procedures, and Work Instructions. Your responsibilities will include: - Assisting Clinical Monitoring staff with site management activities, acting as a Sponsor representative for assigned sites, and ensuring compliance with protocol requirements and study procedures. - Creating and maintaining project files, handling project correspondence, and participating in file audits. - Preparing and updating site manuals, reference tools, and other documents. - Inputting clinical tracking informatio...

Collaborate with cross-functional teams to ensure successful clinical trial execution.Provide medical expertise and guidance on clinical trial protocols and procedures.Conduct thorough reviews of clinical trial data and reports to identify trends Required Candidate profile Strong understanding of clinical trials, including design, conduct, and analysis.Excellent communication and interpersonal skills, with the ability to work effectively with diverse groups.

Manage and oversee the development, implementation, and maintenance of clinical data management systems.Collaborate with cross-functional teams to ensure accurate /timely delivery of clinical data.Develop and implement data quality control process 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

Conduct quality control checks on data accuracy and completeness.Provide training and support to staff on data management best practices.Ensure timely delivery of high-quality data products to stakeholders. Required Candidate profile Strong understanding of clinical trial operations 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. Ability to work effectively in a team environment and communicate complex ideas clearly.

About The Role About The Role Job Title - Research & Development Consultant – Life Sciences Management Level :09,11 Location:Bangalore/ Gurgaon/Hyderabad/Mumbai Must have skills:R&D, Pharmacovigilance, regulatory Reporting Good to have skills:Core LS consulting Job Summary :MBA from a Tier 1 institute or rich relevant industry experience 6+ years of progressive business and/or consulting experience; at least 1 year of experience in Life Sciences industry is mandatory Management consulting and general business consulting experience is a must Familiarity with assets OR tools in business consulting (R&D), such as issue trees, implementation frameworks, diagnosis tools like client questionnaire ...

About The Role About The Role Job Title - Research & Development Consultant – Life Sciences Management Level :09,11 Location:Bangalore/ Gurgaon/Hyderabad/Mumbai Job Summary :MBA from a Tier 1 institute or rich relevant industry experience 6+ years of progressive business and/or consulting experience; at least 1 year of experience in Life Sciences industry is mandatory Management consulting and general business consulting experience is a must Familiarity with assets OR tools in business consulting (R&D), such as issue trees, implementation frameworks, diagnosis tools like client questionnaire and analysis, operating model, business process mapping, and so on. Preferably worked with R&D functi...

About The Role About The Role Job Title - Research & Development Consultant – Life Sciences Management Level :09,11 Location:Bangalore/ Gurgaon/Hyderabad/Mumbai Must have skills:R&D, Pharmacovigilance, regulatory Reporting Good to have skills:Core LS consulting Job Summary :MBA from a Tier 1 institute or rich relevant industry experience 6+ years of progressive business and/or consulting experience; at least 1 year of experience in Life Sciences industry is mandatory Management consulting and general business consulting experience is a must Familiarity with assets OR tools in business consulting (R&D), such as issue trees, implementation frameworks, diagnosis tools like client questionnaire ...

About The Role Job Title - Research & Development Consultant – Life Sciences Management Level :09,11 Location:Bangalore/ Gurgaon/Hyderabad/Mumbai Job Summary :MBA from a Tier 1 institute or rich relevant industry experience 6+ years of progressive business and/or consulting experience; at least 1 year of experience in Life Sciences industry is mandatory Management consulting and general business consulting experience is a must Familiarity with assets OR tools in business consulting (R&D), such as issue trees, implementation frameworks, diagnosis tools like client questionnaire and analysis, operating model, business process mapping, and so on. Preferably worked with R&D functions such as Lab...

About The Role About The Role Job Title - Research & Development Consultant – Life Sciences Management Level :09,11 Location:Bangalore/ Gurgaon/Hyderabad/Mumbai Must have skills:R&D, Pharmacovigilance, regulatory Reporting Good to have skills:Core LS consulting Job Summary :MBA from a Tier 1 institute or rich relevant industry experience 6+ years of progressive business and/or consulting experience; at least 1 year of experience in Life Sciences industry is mandatory Management consulting and general business consulting experience is a must Familiarity with assets OR tools in business consulting (R&D), such as issue trees, implementation frameworks, diagnosis tools like client questionnaire ...

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.

Analyze data and reports to identify trends and areas for improvement.Provide expert guidance on clinical development matters to stakeholders.Ensure timely completion of projects and meet deadlines. Required Candidate profile Strong knowledge of clinical development principles and practices. Excellent analytical and problem-solving skills. Ability to work effectively in a team environment.

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.

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.

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.

Manage and oversee the clinical data reconciliation process to ensure accuracy and quality. Develop and implement effective data reconciliation strategies to identify and resolve discrepancies. Required Candidate profile Strong understanding of clinical data management principles and practices. Proficiency in data analysis and interpretation software. Excellent problem-solving and communication skills.

Develop and implement clinical development strategies to ensure successful project execution. Collaborate with cross-functional teams to design and conduct clinical trials. Required Candidate profile Minimum 3 years of experience in clinical development or a related field. Strong understanding of clinical trial design, conduct, and reporting.

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.

Develop and maintain complex data analysis systems using R and SAS programming languages. Collaborate with cross-functional teams to design and implement data-driven solutions. Required Candidate profile Strong proficiency in R and SAS programming languages. Experience working with large datasets and complex data analysis systems.

Develop and maintain complex data analysis systems using R and SAS programming languages. Collaborate with cross-functional teams to design and implement data-driven solutions. Required Candidate profile Strong proficiency in R and SAS programming languages. Experience working with clinical trial data and regulatory requirements. Excellent analytical, problem-solving, and communication skills.

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.

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 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.

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.