[Urgent Search] Clinical Data Programming
5 hours ago
Job Purpose The incumbent manages Clinical Data Programming to ensure timely creation validation testing implementation and maintenance of databases required across all assigned projects Analyzes study protocol and project requirement s identifies data quality rules and design data entry interfaces in accordance to the study Protocol DMP SOP and all applicable regulatory requirements and standards Key Roles and Responsibilities Deploy complete accurate and efficient clinical study databases to support Data Management and data processing activities Facilitate the preparation transfer and integration of clinical data from internal and external sources into study databases Deliver clinical study data in various formats to key stakeholders as needed Ensure high-quality deliverables and foster strong collaboration with internal and external stakeholders Actively participate in project teams to develop and maintain programs aligned with project standards Manage data exchange with external stakeholders e g labs ECG vendors Safety IDMCs as required Provide ongoing end-user support to project teams to ensure systems and programs function correctly and efficiently Set up and support data review and reporting tools for DM stakeholders including SAS programmers Clinical Medical Pharmacovigilance and Regulatory Affairs and the Study Management Team Offer technical expertise and programming support to projects and data management staff Communicate project status and key issues to DM Management Contribute to the development of new data systems programming procedures and processes Stay current with technological advancements and collaborate with Global Training and IT teams to maximize their application in data management Mentor and train team members while assisting in work delegation Support and maintain standardization of CRF eCRF modules data quality rules data structures libraries code lists and dictionaries in line with CDISC standards Participate in evaluating external vendors and technologies for alignment with project goals and quality standards Identify opportunities for process improvement through standardization and technology to enhance efficiency quality and timeliness of deliverables Advanced Analytics Visualization Responsibilities Strong proficiency in Power BI R and or SAS for programming data listings KRI visuals and developing impactful visualizations that aid cross-functional teams e g Medical Monitors Biostatisticians in drawing meaningful inferences Ability to build analytical models generate reports and design dashboards tailored to business requirements Experience in working with dashboards integrating multiple data sources Excel TXT Oracle SAS using tools like Power BI and SAS Develop listings and respond to ad-hoc requests by producing tables based on supplied shells and support edit checks patient profiles protocol deviations coding reports and other data analysis requirements Qualification Skill and Competencies Requirements Preferably a minimum of a Bachelor s degree in a Life Science Computer Science or related discipline Minimum 8-10 years of clinical data programming experience including working knowledge using clinical data programming tools and applications Experience of leading clinical programming effort across global clinical studies is preferred Job Location Gurugram HR Reporting To Clinical Database Programming Lead CDPL
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Clinical Programmer Ii
1 week ago
Gurgaon, India Syneos Health Clinical Full time**Description** **Clinical Programmer II (eCOA/ePRO)** Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to...
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Medical Writer
5 days ago
Haryana, India Pratham Search Full timeCurrently we required Medical writer for leading medical device company location - Nuh, Mewat, Sohna - Skilled in writing, reviewing and editing scientific medical write-ups including medical studies, drug trials, study reports, white papers, summaries and regulatory documents, or marketing medical writing. - Developing scientific content that is...
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Medical Writer Ii
2 weeks ago
Gurgaon, India Syneos Health Clinical Full time**Description** **Medical Writer II/Sr Medical Editor** Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to...
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Senior Statistical Programmer
2 weeks ago
Gurgaon, Haryana, India beBeeStatisticalProgramming Full time ₹ 20,00,000 - ₹ 25,00,000Statistical Programming LeadWe are seeking an accomplished Statistical Programming Lead to provide comprehensive programming expertise and lead statistical programming activities for clinical studies.Develop and maintain programming documentations following programming standards and processes.Create CDISC standard SDTM mapping specifications and ADaM...
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Clinical Specialist
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Gurgaon, Haryana, India Mölnlycke Full timeManage and implement all regional clinical activities in the designated regionKey Accountabilities Create and drive regional Clinical engagement strategy including the creation of clinical activation plans Leverage existing and build new relationships with regional Key Opinion Leaders KOLs as well as advisory and consultative boards Manage all...
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Clinical Research Manager
7 days ago
Gurgaon, Haryana, India MSD Full timeClinical Research Manager Qualifications Skills Experience This role is primarily accountable for the end-to-end performance and project management for assigned protocols in a country in compliance with ICH GCP and country regulations our company s policies and procedures quality standards and adverse event reporting requirements internally and...
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Clinical Research Manager
1 week ago
Gurgaon, Haryana, India MSD Full time ₹ 15,00,000 - ₹ 28,00,000 per yearJob DescriptionClinical Research Manager:Qualifications, Skills & Experience:This role is primarily accountable for the end-to-end performance and project management forassigned protocols in a country in compliance with ICH/GCP and country regulations,our company's policies and procedures, quality standards and adverse event reportingrequirements internally...
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Gurgaon, Haryana, India MSD Full time ₹ 1,04,000 - ₹ 1,30,878 per yearJob DescriptionThe role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our company's policies and procedures, quality standards and adverse event reporting requirements internally and...
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Clinical Research Manager
1 week ago
Gurgaon, Haryana, India MSD Full time ₹ 15,00,000 - ₹ 28,00,000 per yearJob DescriptionClinical Research Manager:Qualifications, Skills & Experience:This role is primarily accountable for the end-to-end performance and project management for assigned protocols in a country in compliance with ICH/GCP and country regulations, our company's policies and procedures, quality standards and adverse event reporting requirements...
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Gurgaon, Haryana, India Eucloid Data Solutions Pvt Ltd Full timeJob are looking for a highly energetic individual for the SEO Consultant role at Eucloid. The SEO Consultant is responsible for coordinating and implementing search engine marketing programs for clients. The correct person will be goal oriented, possess exceptional attention to detail, and have outstanding interpersonal skills. This is a role that is...
