1999 Clinical Trials Jobs - Page 16

Design, develop, test, and maintain ServiceNow platform following industry leading best practices. Implement and communicate best practice principals for Development & Integration ensuring they are well documented and followed by developers, administrators, and 3rd party vendors. Work closely with cross-functional teams to deliver ServiceNow solutions. Work with the cross-module team to troubleshoot and resolve issues/incidents. Accountable for ServiceNow support and lifecycle management for new and existing ServiceNow Integrations. Collaborate with product owners and stakeholders to ensure requirements are clearly understood and backlog items are prioritized. Demonstrate a flexible and adap...

We re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company If you share our motivations and passion in research, come join us! Primary Purpose Develops, supports, and maintains web-based clinical trials data collection applications under the supervision of senior staff or managers Responsibilities Analyzes requirements Develops, supports, and maintains front-end code, middle tier business logic, backend interfaces Creates and executes unit tests Debugs issues and provides third-tier support Other duties as assigned Qualifications Bachelor s degree in Computer Science or related field Minimum 6 months of relev...

In this pharmacovigilance role, you will carry out processing activities of Individual Case Safety Reports (both clinical trials and post-marketing sources) in the ARGUS Safety database. Processing activities include assessing case validity, undertaking duplicate checks, creating cases in the database, prioritizing cases as per company guidance, updating cases with information provided in XML source documents, identifying adverse events, confirming their seriousness, coding products, undertaking causality and listedness assessments, drafting narratives, determining appropriate case follow-up, reviewing processed cases to verify technical judgment, accuracy, and compliance with company requir...

ORGANISATIONAL OVERVIEW Lambda Therapeutic Research is a Global full-service Clinical Research Organization (CRO) with its headquarters in Ahmedabad, India. With facilities and operations strategically located in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK) and Warsaw (Poland), we offer comprehensive end-to-end clinical research services to the global innovator, biotech, and generic pharmaceutical industries. JOB DETAILS Site Report Management (SRM) - Clinical Trial Operations Review and approve of SVRs for assigned studies and ensure compliance to standard documents as applicable to individual study. Review SVRs to ensure quality, document findings requ...

About The Role Skill required: KYC Screening - Know Your Customer (KYC) Designation: Regulatory Compliance New Associate Qualifications: Any Graduation Years of Experience: 0 to 1 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 AML and Fraud mgmt experience.Understand & implement laws, and regulations designed to stop the practice of generating income through illegal actions during transfer of funds. Anti Money Laundering law covers limited number of transactions and criminal behaviors to prevent terrorist financin...

About The Role Skill required: Clinical Data Services - Clinical Data Management Designation: Clinical Data Svs 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 life enabling them to improve outcom...

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 AML and Fraud mgmt experience.Understand & implement laws, and regulations designed to stop the practice of generating income through illegal actions during transfer of funds. Anti Money Laundering law covers limited number of transactions and criminal behaviors to prevent terrorist financing an...

Role and Responsibilities:As a Senior Research Analyst (Secondary Research) at MakroCare, your role will involve performing comprehensive secondary research to provide detailed information and complete profiles of products You will be responsible for capturing data on companies developing drugs, devices, and other pharmaceutical products from various sources such as press releases, annual reports, clinical trial reports, and more Your primary Responsibilities will include:Grasping new concepts quickly and evaluating scientific data Literature - review, Drug, Medical Devices, Regulatory search and ClinicalTrials review & secondary searchKeeping up-to-date with changes in regulatory legislatio...

Research Analyst - II Roles & Responsibilities: To perform Secondary research in order to provide the detailed information or the complete profile of the product. Thorough understanding of regulations, Ability to grasp new concepts quickly and to assimilate and evaluate scientific data keeping up to date with changes in regulatory legislation and guidelines Strong secondary research skills and Sound Knowledge on drug labels and clinical trial Knowledge on drugs, devices and other products regulations Able to evaluate applicable laws and regulations to determine impact & Able to mentor team members Compile and analyze data using modern and traditional methods to collect it. Responsible for co...

R & D Biomedical Engineer- Biomedical Engineering, Medical Devices Manufacturing, or Clinical Trials An R & D Biomedical Engineer is a highly experienced professional specializing in the research and development of biomedical technologies. They are responsible for designing, developing, and optimizing medical devices and systems that enhance healthcare delivery. Their expertise ensures innovation in medical technologies, contributing to the advancement of patient care, while ensuring compliance with regulatory standards. By leading the development of cutting-edge solutions, they play a key role in improving the safety, functionality, and reliability of critical healthcare equipment. Primary ...

JOB DESCRIPTION: MAIN PURPOSE OF ROLE Experienced professional individual contributor that works under limited supervision. Applies subject matter knowledge in the area of Medical Affairs. Requires capacity to apply skills/knowledge within the context of specific needs or requirements. MAIN RESPONSIBILITIES .As the Experienced professional in the Medical Affairs Sub-Function, possesses well developed skills in overseeing the direction, planning, execution, clinical trials/research and the data collection activities. .Contributes to implementation of clinical protocols, and facilitates completion of final reports. .Recruits clinical investigators and negotiates study design and costs. .Respon...

Challenging. Meaningful. Life-changing. Those aren t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of c...

The GCP Compliance Manager (GCO) is responsible for overseeing and controlling compliance of regulated GCO activities, focusing on those with a high impact on GCO's ability to meet objectives. This role plays a crucial part in supporting GCP Compliance pillars, including issue management, audits, and inspections, particularly system/process audits and global inspections for authorizations and GCO self-strategy delivery. As the GCP Compliance Manager (GCO), you will provide GxP expertise and support GCP Compliance for various functions, compliance, process, training, and risk groups. Your responsibilities will include managing systemic quality issues, deviations, quality events, audits, and i...

As a Pharmacology Research Lead, you will be responsible for overseeing and managing pharmacological research projects from their initiation to completion. Your role will involve designing and conducting experiments to assess the efficacy and safety of drugs, as well as analyzing pharmacokinetic and pharmacodynamic data to guide drug development processes. You will also be tasked with developing dosage forms and delivery mechanisms for specific therapeutic areas and collaborating with interdisciplinary teams to enhance research methodologies. In addition to conducting research activities, you will be expected to prepare and deliver comprehensive reports on research outcomes, ensuring complia...

At Allucent, you will play a crucial role in helping small-medium biopharmaceutical companies navigate the world of clinical trials to deliver life-changing therapies to patients worldwide. As a Sr. Clinical Research Associate Contractor (Sr.CRA) on our remote A-team, you will have the opportunity to independently manage and monitor investigational sites, ensuring adherence to trial protocols, SOPs, regulations, and Good Clinical Practice standards. Your responsibilities will include maintaining the highest quality standards for trial monitoring activities, overseeing site activities to ensure protocol compliance, preparing detailed reports, updating CTMS systems, and providing support to th...

Responsibilities: Conduct clinical trials with precision Manage clinical data accurately Collaborate on drug safety initiatives Ensure compliance with regulatory standards Monitor adverse events promptly

Department / Process: Sales Enablement Analyst Location: Mumbai Job Description: As an Analyst for Sales Enablement, this role will be responsible for designing impactful and visually engaging PowerPoint presentations that clearly convey our sales strategies, product offerings, and value propositions to prospective clients Additionally, youll contribute to creating sales training content, KPI reporting, and performance dashboards, Collaborating closely with the sales team, you will translate complex data and insights into clear, concise, and compelling visual content Utilizing tools such as Salesforce and Google Analytics, you will monitor leads, opportunities, and customer interactions, Exp...

ABOUT US: Notion Press is Indias largest book publishing platform with over 100,000 books published and sold in 150+ countries We are a 13-year-old platform and currently publish a new book every 30 minutes Notion Press is a global platform for anyone who believes in the power of words and the impact it can have on the world we live in Our vision is to democratize publishing and help writers to publish and sell their books directly to readers around the world We are a 120+ strong team currently operating in India, looking to expand to South-East Asia, Europe and North America, We are seeking a driven, self-motivated candidate to join our growing organization In this position, you will be res...

The SAS Programmer will be responsible for providing SAS programming support for the Statistics and Data Management functions for all clinical trials and regulatory submissions. The candidate will work closely with Biostatisticians and Data Managers to create SAS programs for independently validating selected tables, listings, and figures and to assist with data cleaning and query generation. This position will also serve as a contact for programming activities being performed. Key Activities: Perform data manipulation techniques and advanced techniques (arrays, transpositions, complex merges, SQL, SDTM etc.) and generic macro use and development to enable listing, table, and graph generatio...

Project Role : Application Lead Project Role Description : Lead the effort to design, build and configure applications, acting as the primary point of contact. Must have skills : SAP HCM Payroll Good to have skills : NAMinimum 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Application Lead, 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 ensure that application development aligns with business objectives, overseeing project timelines, and facilitating communication among stakeholders to drive successful p...

Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services New Associate Qualifications: Bachelor of Pharmacy/Bachelor of Physiotheraphy/BSc. Nursing Years of Experience: 0 to 1 years About Accenture Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Visit us at www.accent...

Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services New Associate Qualifications: Bachelor of Pharmacy,BSc. Nursing,Bachelor of Physiotheraphy Years of Experience: 1 to 2 year About Accenture Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Visit us at www.accentu...

Flipkart is looking for Manager - Central to join our dynamic team and embark on a rewarding career journey Delegating responsibilities and supervising business operations Hiring, training, motivating and coaching employees as they provide attentive, efficient service to customers, assessing employee performance and providing helpful feedback and training opportunities. Resolving conflicts or complaints from customers and employees. Monitoring store activity and ensuring it is properly provisioned and staffed. Analyzing information and processes and developing more effective or efficient processes and strategies. Establishing and achieving business and profit objectives. Maintaining a clean,...

Job Title: AGM / DGM – Clinical Trials (Protocol & Report Writing) Department: Clinical Research / Clinical Operations Minimum 10–15 yrs of relevant experience in clinical trials, protocol writing, CSR writing, and regulatory documentation

We are seeking a highly motivated and detail-oriented Research Ops Intern- Clinical Data to join our dynamic team. The ideal candidate will have a strong background in oncology, the ability to understand and interpret medical terminology from Electronic Health Records (EHR) and medical reports, and the expertise to extract and analyze data from patient notes. The candidate must have a background of clinical research and is able to comprehend clinical trials. Also have good knowledge about patient pre-screening, enrolling participants in oncology clinical trials . The role requires proficiency in Google Sheets and Excel, along with the ability to correlate medical data to meet specific requir...