6754 Clinical Research Jobs - Page 49

Design, develop, and maintain complex statistical analysis systems using SAS.Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Required Candidate profile Strong knowledge of SAS programming language and its applications in clinical trial data management. Experience with SQL database management systems and querying languages.

About The Role Skill required: Regulatory Services - Life Sciences Regulatory Operations Designation: LifeScience Regulatory Svs Associate Qualifications: 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 life ¢- enabling them to improve outcomes...

Design, develop, and maintain clinical databases 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 management systems. Understanding of database design principles and data modeling techniques.

Develop high-quality medical documents, including reports, notes, and correspondence.Review and edit medical records for accuracy, completeness, and compliance with regulations. Required Candidate profile Strong knowledge of medical terminology, anatomy, and physiology. Excellent writing, editing, and communication skills. Ability to work independently and as part of a team.

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...

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 efficient data processing Required Candidate profile Strong knowledge of SAS programming language and its applications in clinical trial data management. Experience with SQL programming language and database management systems.

Monitor medical enquiries and respond to queries from clients and stakeholders.Provide excellent customer service and ensure timely resolution of medical inquiries. 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.

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.

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.

Develop high-quality written materials 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 3 years of experience in medical writing or a related field. Strong understanding of medical terminology, anatomy, and physiology. Excellent writing, editing, and communication skills.

About The Role Skill required: Pharmacovigilance Services - Safety Writing Designation: Pharmacovigilance Services Sr Analyst Qualifications: Bachelor 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 life ¢- enabling them to improve outcomes by converg...

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 case report forms.

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.

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 Strong knowledge of Good Clinical Practice (GCP) principles and regulations. Experience in conducting clinical trials, including protocol development, site management, and data analysis.

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 medical content for various platforms, including reports and presentations.Conduct research and analyze data to create accurate and informative medical documents. Required Candidate profile Strong understanding of medical terminology and concepts. Excellent communication skills. Ability to work independently and as part of a team. Proficient in using computer software applications

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.

Conduct thorough medical device safety assessments and evaluationsDevelop and implement effective safety protocols and proceduresCollaborate 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.

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.

Develop and maintain databases, spreadsheets, and reports for tracking and analyzing clinical trial data.Collaborate with cross-functional teams to ensure accurate and timely delivery of high-quality results. Required Candidate profile Strong knowledge of SAS programming language and its applications in clinical trial data analysis. Experience with Veeva or similar systems is desirable.

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 trials. Experience in managing clinical data in a fast-paced environment. Excellent analytical and problem-solving