1035 Argus Jobs - Page 2

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...

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 and concepts. Excellent analytical and problem-solving skills. Ability to work effectively in a fast-paced environment with multiple priorities.

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 ...

Conduct thorough medical reviews of patient records, including diagnoses, treatments, and test results.Analyze medical data to identify trends, patterns, and areas for improvement.Collaborate with healthcare professionals to develop. Required Candidate profile Effective communication and interpersonal skills for collaboration with healthcare teams. Strong organizational and time management skills with the ability to meet deadlines.

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.

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.

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

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.

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.

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.

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.

Conduct clinical trials to ensure compliance with regulatory requirements and company protocols. Collaborate with cross-functional teams to design, implement, and monitor clinical trial protocols. Required Candidate profile Minimum 3 years of experience in clinical trials, preferably in a pharmaceutical industry setting.Strong knowledge of Good Clinical Practice (GCP) principles and regulations governing clinical trials.

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.

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.

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.