3474 Clinical Trials Jobs - Page 35

About The Role Skill required: KYC Screening - Know Your Customer (KYC) Designation: Regulatory Compliance Associate Qualifications: Any Graduation Years of Experience: 1 to 3 years What would you do? Help clients transform their compliance function from reactive to proactive through an intelligent compliance operating model powered by data, intelligent technologies and talentLooking for someone with KYC experience along with ECDD/OCDD knowledgeBusiness and regulatory requirements, governance, operating model, process and system controls to verify the identity, suitability, and risks involved with onboarding and/or maintaining a business / customer relationship. This includes driving custome...

About The Role Project Role : Application Designer Project Role Description : Assist in defining requirements and designing applications to meet business process and application requirements. Must have skills : Workday UK Payroll Good to have skills : Workday US Payroll Minimum 7.5 year(s) of experience is required Educational Qualification : 15 Years full time education Experience is required in the primary skill of the RRD. Mandatory certification in core skill required. Certification in specialized skill is optional Summary :As an Application Designer, you will assist in defining requirements and designing applications to meet business process and application requirements. A typical day i...

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 Skill required: Pharmacovigilance Operations - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services New Associate Qualifications: Bachelor of Pharmacy/Master of Pharmacy Years of Experience: 0 to 1 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 t...

About The Role Skill required: KYC Screening - Sanctions Screening Designation: Regulatory Compliance Analyst Qualifications: Any Graduation Years of Experience: 3 to 5 years What would you do? Help clients transform their compliance function from reactive to proactive through an intelligent compliance operating model powered by data, intelligent technologies and talentLooking for someone with KYC experience along with ECDD/OCDD knowledgeAbility to effectively and efficiently conduct the process of screening individuals, entities, or transactions against lists of sanctioned or restricted parties. Sanctions screening involves using specialized software, understanding relevant regulations, and...

Assist in planning, initiation, and execution of clinical trials. Conduct site monitoring visits and ensure adherence to study protocols, SOPs, and regulatory requirements. Please call- 7026629008 / 8050011327 for further details.

UG Training Academy is looking for Freshers Trainee Medical coders to join our dynamic team and embark on a rewarding career journey Collaborate with cross-functional teams to achieve strategic outcomes Apply subject expertise to support operations, planning, and decision-making Utilize tools, analytics, or platforms relevant to the job domain Ensure compliance with policies while improving efficiency and outcomes Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before applying.

Sponsor-dedicated: Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, youll be at the heart of our clients innovation. As a Principal Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program. Position Overview: This position reports to the Director, Biostatistics and Programming in the FSP Services business unit in Cytel. The Principal Statistical Programmer works independently with only concept level instructi...

ROLE SUMMARY As part of the Clinical Data Sciences group, an integral delivery unit within the Clinical Development & Operations (CD&O) organization, the Senior Central Testing Analyst is responsible for leading the Database Testing and validation activity at a study or asset level and performing testing of database (UAT) and ensuring that the CRFs are designed in accordance to protocol and the end users are able to enter the data as per the standards and expectation. In addition to the screen testing the Senior Central Testing Analyst will also be responsible to perform the testing of data specification to ensure that the checks are rightly programmed, appropriate and adequate as per the pr...

Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, youll be at the heart of our clients innovation. As a Senior Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program. Position Overview: As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed...

The DO/GS organization is actively looking for a motivated candidate . In this role, you will be responsible for driving IT quality & compliance, and assurance across Lilly s mission-critical systems spanning across various business functions. Innovation & Automation : Drive innovation in validation by exploring and leveraging AI, digital tools, and automation technologies to streamline validation documentation and operational compliance . Identify opportunities to simplify and automate IT system operational compliance activities through digital tools or AI-enabled solutions and adoption of risk-based approaches and automation frameworks . Continuously evaluate emerging technologies (eg, AI-...

Roles and Responsibility Assist in the development of new X-ray techniques and protocols. Collaborate with cross-functional teams to design and implement experiments. Analyze data from X-ray experiments to draw meaningful conclusions. Develop and maintain accurate records of experiments and results. Participate in quality control and quality assurance activities. Stay updated with the latest advancements in X-ray technology and techniques. Job Requirements Strong understanding of biotechnology, pharmaceuticals, or clinical research principles. Excellent analytical and problem-solving skills. Ability to work effectively in a team environment. Strong communication and interpersonal skills. Fam...

Lead Generation: Perform research on potential clients product portfolios (including products under development) and identify decision-makers. Send focused emails and make cold calls to introduce ClinChoice s solutions and generate leads. Meet monthly and quarterly targets to obtain meetings with prospective clients. Maintain an accurate and updated database of contacts, meetings, and next steps in ClinChoice s sales systems. Cross-departmental Collaboration: Partner with the business insights team to identify opportunities, provide inputs for custom content, and distribute marketing assets. Research and Learning: Remain up to date with ClinChoice s capabilities, service offerings, and ongoi...

Develop and contribute to frontend and backend frameworks supporting business-critical applications. Design and build scalable, reusable, and maintainable backend services and APIs. Replace commercial off-the-shelf (COTS) systems with modern, in-house scalable solutions. Develop user-facing interfaces using React.js, Angular, or Vue.js with a focus on performance and accessibility. Coach and mentor junior engineers and help raise the overall technical bar. Help define and maintain engineering standards, including CI/CD and code quality practices. Collaborate across teams to deliver impactful features with measurable value. Key Responsibilities Backend Development Experience with backend prog...

Job Summary We are seeking a highly skilled and proactive Veeva CTMS Subject Matter Expert (SME) to join our consulting firm and support our Life Sciences clients in optimizing clinical trial management processes. This role will be responsible for managing Veeva CTMS, eTMF, EDC implementations, ensuring compliance, and enabling efficient trial lifecycle management for our clients. Key Responsibilities Act as the subject matter expert (SME) for Veeva CTMS, eTMF, and EDC across our Life Sciences consulting projects. Lead end-to-end configuration of Veeva CTMS, eTMF, and EDC to support clinical trial planning, execution, data management, and reporting for various clients. Manage stakeholder rel...

Role Python Developer Experience 4-7 Years Location Any EY Location Must Have Strong hands on exp in Python, Pandas, Numpy, Experience on ETL Manage large datasets Multi threading and Object Oriented Concepts of Python Automation on Excel using Python SQL Hands on exposure in Data Science & AI technologies Good to Have Domain expertise in pharma domain especially having deep exposure in clinical trials, biostats modelling etc exp working on packages like pywin32, Win32Com Experience or understanding of at least 1 cloud stack AWS/ Azure/ GCP Experience on Apache Air flow, Alteryx .jobDisplay { padding-top40px;}div#search-wrapper { displaynone;}

Job Summary We are seeking a highly skilled and proactive Veeva CTMS Subject Matter Expert (SME) to join our consulting firm and support our Life Sciences clients in optimizing clinical trial management processes. This role will be responsible for managing Veeva CTMS, eTMF, EDC implementations, ensuring compliance, and enabling efficient trial lifecycle management for our clients. Key Responsibilities Act as the subject matter expert (SME) for Veeva CTMS, eTMF, and EDC across our Life Sciences consulting projects. Lead end-to-end configuration of Veeva CTMS, eTMF, and EDC to support clinical trial planning, execution, data management, and reporting for various clients. Manage stakeholder rel...

Your key responsibilities At an associate level your primary responsibilities require you to Understand the underlying issues of a project. Follow step by step process of researching the issues and presenting the findings in the desired format. Understand legal writing and uses appropriate and pre-discussed formatting while presenting their findings. Interpret statutes and regulations correctly. Apply themselves to understanding case law. Be thorough and meticulous with great attention to details. Achieve on time delivery (OTD) on client deliverables Attend mandatory training and certification courses. Co-operate with team members and acts as a team player. Escalate project specific issues t...

Your key responsibilities Good grasp of baseline U.S. Foreign Account Tax Compliance Act (FATCA) regulation Knowledge of tax technical issues and processes relevant to U.S. individual and non- individual entities; familiarity with IRS forms W-8 and W-9 requirements Consistently provide high quality work with integrity and be vigilant to audit standards and requirements Contribute to client satisfaction by providing timely and effective responses to client needs and concerns Act as a counsellor for Analysts and Advanced Analysts (where applicable) Develop and supervise staff on all technical, client service and engagement management skills, including providing input in performance discussions...

As a Principal Statistical Programmer within our Hyderabad Hub, youll be part of a performing team, delivering biostatistics and programming activities throughout the Vaccines R&D value chain (Pre-Clinical, Clinical, Translational, CMC) with our Vaccines Global Biostatistical Sciences team. We are an innovative global healthcare company that helps the world stay ahead of infectious diseases by delivering more than 500 million vaccine doses a year. Across different countries, our talented teams are exploring new technologies to protect people and promote healthy communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients arou...

Main responsibilities: The Principal Statistical Programmer will work with Medical Affairs biostatisticians and/or programmers and Sanofi Business Operations biostatistics and programming personnel to implement statistical analysis plans and provide QCd data packages including tables, figures, and listings for use in publications (i.e. abstracts, posters, oral, presentations, manuscripts and ad-hoc data analysis requests);The Principal Statistical Programmer will develop, implement, and document non-routine macros and advanced techniques; The Principal Statistical Programmer will ensure SOPs are followed and timelines and quality are met; Collaboration of Local biostatistics and programming ...

We are looking for a highly motivated and detail-oriented individual to join our team as a Trainee Medical Reviewer in Bengaluru. The ideal candidate should have 0-1 years of experience. Roles and Responsibility 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 and implement effective treatment plans. Maintain accurate and up-to-date records of patient information and review findings. Participate in quality improvement initiatives to enhance patient care and outcomes. Develop and maintain knowledge of medical ...

Databriks + Pyspark About The Role ::1 Skill:Databriks + Pyspark Exp 5 to 8 yr Location Any PSL , Bangalore, Delhi, Pune , Chennai Dont look for Hyderabad Location Azure Data bricks,PySpark,Oracle PL SQL,ETL,SQL,Data Integration Data Engineer - Data AnalystSummaryStrategically manages and maintains corporate global clinical data for all major business units, while ensuring data quality and integrity. Provides system support, testing, and training for applications accessing clinical data.Proven 2-5 years work experience as a Data Analyst in Clinical data Identifies, investigates, and resolves data quality issues, communicating with business units and IT and performing root cause analysis as n...

Position Summary: • We are looking out for a Senior Clinical Data Associate who will be working on Beacon Targeted Therapies (https://beacon-intelligence.com); a database from our UK based Client, Hanson Wade. • Beacon is a drugs, clinical trials, deals & companies intelligence database based on modular solutions focusing on various therapeutic areas. • The content is manually curated by researchers providing in-depth data to help identify the most relevant trends in the landscape. You will be part of a global network of life science researchers working on dynamic, fast growing products in exciting, cutting-edge life science areas. Key Accountabilities / Responsibilities: • Lead and manage r...

Responsibilities: * Manage clinical data from study start to closeout using RAVE software. * Collaborate with cross-functional teams on EDC setup and maintenance.