609 Case Processing Jobs - Page 2

Coordinate and prepare regulatory submissions, including applications, reports, and other documents.Ensure compliance with relevant laws, regulations, industry standards.Develop and maintain relationships with regulatory authorities 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.

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.

Conduct thorough medical reviews and assessments to ensure compliance with regulatory requirements.Develop and implement effective monitoring strategies to track patient safety and efficacy. Required Candidate profile Strong understanding of clinical development principles and practices.Excellent analytical and problem-solving skills, with attention to detail and the ability to interpret complex data.

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. Required Candidate profile Strong understanding of employment firms and recruitment services.Excellent publishing skills, with attention to detail and ability to meet deadlines.Ability to work independently

Coordinate and prepare regulatory submissions, including applications, reports, and other documents.Ensure compliance with relevant laws, regulations, and industry standards. 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.

Develop and implement effective aggregate reporting strategies to meet business objectives.Analyze complex data sets to identify trends,patterns, providing insights to stakeholders.Create comprehensive reports using various tools and technologies 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.

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 database management.

About The Role Project Role : Quality Engineer (Tester) Project Role Description : Enables full stack solutions through multi-disciplinary team planning and ecosystem integration to accelerate delivery and drive quality across the application lifecycle. Performs continuous testing for security, API, and regression suite. Creates automation strategy, automated scripts and supports data and environment configuration. Participates in code reviews, monitors, and reports defects to support continuous improvement activities for the end-to-end testing process. Must have skills : Oracle Argus Good to have skills : NA Minimum 3 year(s) of experience is required Educational Qualification : 15 years fu...

About The Role Skill required: Pharmacovigilance Operations - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services Associate Qualifications: Bachelor of Pharmacy/Master of Pharmacy Years of Experience: 1 to 3 years What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vision to li...

About The Role Project Role : Business Architect Project Role Description : Identify opportunities to deliver tangible business value by assessing the current state, capturing high-level requirements, and defining business solutions. Translate business needs into technology-enabled solutions and operating models. Support transformation by developing business cases and guiding implementation of key initiatives. Must have skills : Oracle Argus Good to have skills : NA Minimum 3 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As a Business Architect, you will identify opportunities to deliver tangible business value by assessing the current st...

Conduct thorough medical reviews of patient records, including diagnoses,treatments, and test results.Analyze medical data to identify trends,areas for improvement.Collaborate with healthcare professionals to develop effective treatment plans. Required Candidate profile Strong knowledge of medical terminology, anatomy, and physiology. Ability to work effectively in a fast-paced environment with multiple priorities. Effective communication and interpersonal skills.

About The Role Skill required: Pharmacovigilance Operations - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services Analyst Qualifications: Bachelor of Pharmacy/Master of Pharmacy Years of Experience: 3 to 5 years What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vision to life...

About The Role Skill required: Pharmacovigilance Operations - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services Sr Analyst Qualifications: Bachelor of Pharmacy/Master of Pharmacy Years of Experience: 5 to 8 years What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vision to l...

About The Role Project Role : Software Development Lead Project Role Description : Develop and configure software systems either end-to-end or for a specific stage of product lifecycle. Apply knowledge of technologies, applications, methodologies, processes and tools to support a client, project or entity. Must have skills : Veeva Vault Good to have skills : NA Minimum 7.5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As a Veeva Safety Application Development SME, you will lead the effort to design, build, and configure applications, acting as the primary point of contact. Your typical day will involve collaborating with various teams to ...

About The Role Skill required: Pharmacovigilance Operations - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services Specialist Qualifications: MBBS Years of Experience: 7 to 11 years What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vision to life ¢- enabling them to improve ou...

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 Familiarity with electronic health records (EHRs) and other healthcare software systems. Strong organizational skills with the ability to prioritize tasks and manage multiple projects simultaneously.

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 patient records, including diagnoses, treatments, and test results.Analyze medical data to identify trends, patterns, and areas for improvement. Required Candidate profile Strong knowledge of medical terminology, anatomy, and physiology. Ability to work effectively in a fast-paced environment with multiple priorities. Effective communication and interpersonal 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 Skill required: Finance & Accounting - Operational Audit & Compliance Designation: Quality Auditing Specialist Qualifications: Chartered Accountant Years of Experience: 7 to 11 years What would you do? You will be aligned with our Finance Operations vertical and will be helping us in determining financial outcomes by collecting operational data/reports, whilst conducting analysis and reconciling transactions.As an audit specialist on the internal audit team, you will conduct process audits, identify gaps, report findings, manage schedules, and ensure actions are taken to mitigate risks. You will interact with clients and oversee medium-small teams or individual tasks. Your mai...

About The Role Project Role : Quality Engineer (Tester) Project Role Description : Enables full stack solutions through multi-disciplinary team planning and ecosystem integration to accelerate delivery and drive quality across the application lifecycle. Performs continuous testing for security, API, and regression suite. Creates automation strategy, automated scripts and supports data and environment configuration. Participates in code reviews, monitors, and reports defects to support continuous improvement activities for the end-to-end testing process. Must have skills : Oracle Argus Good to have skills : NA Minimum 3 year(s) of experience is required Educational Qualification : 15 years fu...

About The Role Skill required: Pharmacovigilance services - Safety Writing Designation: Pharmacovigilance Services Analyst Qualifications: Bachelor of Pharmacy Years of Experience: 3-5 Yrs What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vision to life ¢- enabling them to improve outcomes by converging arou...

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 Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services Analyst Qualifications: Bachelor of Pharmacy/Bachelor Degree in Life Sciences Years of Experience: 3 to 5 years What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vi...

Develop high-quality medical content for various platforms, including reports and presentations.Conduct research and analyze data to create accurate and informative medical documents. Required Candidate profile Minimum 2 years of experience in medical writing or a related field. Strong understanding of medical terminology and concepts. Excellent writing, editing, and communication skills.