8317 Clinical Research Jobs - Page 30

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...

Skill required: Marketing Operations - Medical Affairs Designation: Copywriting Senior Analyst Qualifications: Any Graduation Years of Experience: 5 to 8 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.accenture.com What would you do Help balance increased marketing complexity and diminishing marketing...

About The Role Skill required: Com.Bkg- Commercial Real Estate - Real Estate Due Diligence Designation: Banking Advisory Associate Qualifications: Any Graduation Years of Experience: 1 to 3 years What would you do? We help clients address quality and productivity issues, keep pace with customer expectations, navigate regulatory and operational pressures and ensure business sustainability by transforming their banking operations into an agile, resilient operating model.The Corporate banking /Wholesale banking team is responsible for helping clients and organizations processes trade finance transactions by providing superior service delivery to trade customers whilst safeguarding the bank from...

About The Role Project Role : Software Development Engineer Project Role Description : Analyze, design, code and test multiple components of application code across one or more clients. Perform maintenance, enhancements and/or development work. Must have skills : SAP HCM Payroll Good to have skills : NA Minimum 7.5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As a Software Development Engineer, you will engage in a variety of tasks that involve analyzing, designing, coding, and testing multiple components of application code across various clients. Your typical day will include collaborating with team members to perform maintenance and e...

Position Overview We are seeking an experienced Associate Manager - CDM to support our clinical data management team in Chennai. The successful candidate will work as Subject Matter Expert (SME) for CRIO CTMS including e-Source creation, edit, oversee and mentor the end-to-end clinical trial management system activities, ensuring seamless integration between CTMS, EDC platforms, and clinical operations Key Responsibilities CTMS Operations & Strategy Develop and maintain e-source, CTMS workflows, user roles, and system permissions. Ensure integration between CTMS and EDC systems for seamless data flow. Lead system upgrades, validation activities, and change control processes. Establish and mo...

Your role and responsibilities Building and delivering IS Risk Assessment Service as part of the Compliance and Risk Assessment Department. You will be mainly accountable for: Responsibility for defining, designing, implementing, managing security risk assessments and the regulatorycompliance assessments Ensuring targets achievement in cooperation with customers within the budget Providing service management knowledge to the team, vendors and stakeholders and managing expectations Incident and service improvement management Attending service review, service level agreement and operational level agreement meetings Qualifications for the role Degree in IT field 10 years of experience in servic...

Skill required: Clinical Data Services - SAS Clinical Designation: Clinical Data Svs Associate Qualifications: BE/MSc/Bachelor 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 world s leading biopharma companies bring their vision to life enabling them to improve outcomes by converging around the patient, co...

Job Overview: Manages ARC review and are responsible for performing TMF review of electronic Trial Master Files (eTMF), Trial, Country, and Site artifacts for clinical studies in support of sponsors services contracts and internal business needs. Summary of Responsibilities: Position provides process, control, coordination, and approval of clinical trial documents. Position is responsible for ECD, Phase I-IV electronic trial master file (eTMF). Maintains an understanding of applicable regulatory requirements. Managing electronic Trial Master Files (eTMF), (Trial, Country, and Site artifacts) for clinical studies in accordance with TMF processes, working with key study personnel such as the S...

Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and practices. Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. Clinical Project leads can run their own studies. The Project Lead focus is on leveraging therapeutic expertise and IQVIA s suite of solutions to drive operational excellence and strat...

Job Overview Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and practices. Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. Clinical Project leads can run their own studies. The Project Lead focus is on leveraging therapeutic expertise and IQVIA s suite of solutions to drive operational excelle...

About The Role Discover Journals aim to support researchers in communicating and advancing discovery for a better world. We do this by providing a trusted environment in which researchers can quickly, easily and transparently share their discoveries, data and research stories by publishing in peer-reviewed journals with an inclusive editorial threshold. We are seeking a Senior Editor on our Discover journals to manage the launch and development of a portfolio of new journals with a strong focus on medicine, public health, and clinically oriented research. The role centers on maintaining the highest standards of research integrity, ensuring an efficient and rigorous peer-review process, and d...

We are seeking an exceptional, experienced senior immunologist with specific expertise in T-cell biology, hands-on experience with T-cell isolation, stimulation and enrichment protocols, in-depth knowledge of TCR discovery, and assays related to measuring T-cell potency and cytokine release. RESPONSIBILITIES Maintenance and handling of primary immune cells from various sources Contribute to the design of TCRs and TCR-mimics Lead discovery campaigns to generate TCRs via stimulation assays (medium throughput or high throughput fashion) Plan and execute in vitro and in vivo experiments to comprehensively characterise the potency of both designed and discovered TCRs. Lead communication and drive...

Job Description Location: Bengaluru (highly preferred); PAN India considered if suitable candidates are unavailable Contract Length: 6 months (extendable) Japanese Vietnamese French Arabic Persian Or a combination of any two languages from the above Role Overview We are seeking candidates with backgrounds in Pharma, Nursing, Medical, Dentistry, or Life Sciences who also hold linguistic certifications (A1/A2/B1/B2) in one or more of the following languages: Japanese, Vietnamese, French, Arabic, Persian, or a combination of any two. The ideal candidate will be comfortable working in the Pharmacovigilance (PV) domain and possess strong communication and analytical skills. Key Responsibilities R...

Responsibilities Perform a wide range of interventional cardiology procedures, including angioplasty, stenting, and catheterization, ensuring the highest standards of patient care and safety Collaborate with a multidisciplinary team of healthcare professionals to develop and implement individualized treatment plans for patients with cardiovascular conditions Conduct thorough patient assessments to diagnose and manage cardiovascular diseases, employing advanced diagnostic tests and medical imaging Provide expert consultation to patients and their families, addressing concerns and educating them on treatment options and lifestyle modifications for improved heart health Participate actively in ...

PopVax is an Indian full-stack biotechnology company developing novel mRNA vaccines and therapeutics using computational protein design. Our first vaccine is a next-generation COVID-19 booster, which will enter a first-in-human Phase I clinical trial in the U.S. early this year. This vaccine is intended to broaden protection against both current and predicted future SARS-CoV-2 variants, reducing the possibility of a new mutation in the virus suddenly causing another massive wave of infection. We have a preclinical pipeline of 6 additional novel vaccine candidates built on our mRNA-LNP platform that we will be taking into clinical trials over the next few years. Our work to date has been fund...

Regulatory Scientist - India - Office or Home ICON plc is a world-leading healthcare intelligence and clinical research organization. We re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Regulatory Scientist to join our diverse and dynamic team. In this role, you will support regulatory submissions for clinical trials in India and ensure alignment with applicable regulatory frameworks, contributing to the advancement of innovative therapies in partnership with leading pharmaceutical and biotech organizations. What you will be doing Supporting and ex...

A Day in the Life Responsibilities may include the following and other duties may be assigned. Candidate should have 10 years of experience into clinical data management and 2+ years of experience into people management. Provides leadership for the conduct of clinical studies and for the regulatory affairs function as it applies to product approval. Studies must be scientifically valid, meet all relevant regulatory requirements and be conducted within ethical guidelines. The end result of the clinical studies must be a fair assessment of the safety and efficacy of the tested product (s) and attainment of product approvals in a timely matter. Develops and implements regulatory strategies to o...

We are looking for a highly skilled Senior Scientific Writer to join our team in the Medical Communication/Publications department at Merck Group. The ideal candidate will have a strong background in medical writing and excellent communication skills. Roles and Responsibility Develop high-quality, peer-reviewed publications for various medical journals. Collaborate with cross-functional teams to create engaging and informative content. Conduct thorough research and analysis to stay updated on industry trends. Create and edit manuscripts, posters, and other visual materials for conferences and meetings. Work closely with internal stakeholders to develop marketing materials and communications....

***Greetings from You & I Consulting*** You & I Consulting has always been in the spotlight for getting placed in 64+ MNC's PAN India. Hirings for MNC: - Great Opportunity in Giant MNC . Grab the Opportunity to grow and explore. Statistical Programmer!!! We are hiring for: Statistical Programmer up to 20 lpa ctc Experience Level: 5 to 15 years Location- Mumbai, Pune, Noida, Bangalore Job Description: We are looking for a skilled Senior Statistical Programmer I / II to join our team at Icon Pharmaceuticals. The ideal candidate will have a strong background in statistical programming and analysis, with excellent problem-solving skills and attention to detail.. Key Responsibilities: Develop and...

LTFinance is looking for TEAM MEMBER - QUALITY ASSURANCE to join our dynamic team and embark on a rewarding career journey Collaborate with cross-functional teams to identify and mitigate risks, ensuring compliance with regulatory requirements. Develop and implement effective quality control processes to ensure high standards of service delivery. Conduct regular audits and reviews to identify areas for improvement and provide recommendations for enhancement. Analyze data and metrics to measure performance and identify trends for improvement. Provide training and coaching to team members on quality procedures and best practices. Foster a culture of continuous improvement, encouraging team mem...

Role Overview: As an Analyst Clinical Research, you will play a key role in developing two main artefacts: Human Readable and Data Dictionary using MAT tool. You will analyze measure specifications to translate data into clinical form while working closely with clinical teams, database management personnel, and project managers. Key Responsibilities: - Registry Data Management: - Create two main artefacts: Human Readable and Data Dictionary. - Maintain the artefacts for every performance year. - Analyze CMS published documents for any updates. - Ensure timely and accurate submission of required registry reports. - Data Analysis & Reporting: - Analyze codes for annual updates and code cleanin...

As a Proposal, Budget and Contracts Associate at Novotech, your role involves developing and preparing proposals, budgets, and contracts for new business. You will work closely with the Business Development team and Project Managers to ensure the timely delivery of high-quality documents that accurately reflect customer requirements. Your key responsibilities include: - Developing proposals by preparing high-quality materials, collating content, ensuring readability and consistency in formatting, and researching and presenting statistics and company information. - Creating budgets for projects based on client information, preparing other budget elements, liaising with vendors for quotations,...

Summary To write, support, manage and provide consultancy to senior and expert scientific writers to prepare all high quality medical and scientific communications including literature review, abstracts, posters, slide decks, Manuscripts (complex) for publication/ presentation. About The Role Principal Scientific Writer Location Hyderabad Hybrid Major Responsibilities Prepares / supports the preparation of highly complex scientific documents to meet highest quality standards. Initiates, implements and champions process improvement techniques. Manages multiple projects across multiple brands and therapeutic areas. Defines and implements stakeholder management strategies and tactics. Develops ...

Consultant – Cardiology (DRNB/DM, 5–8 years) Consultant – Paediatric Intensive Care (DRNB/DM, 1–2 y) Consultant – Neonatology (DRNB/DM, Senior Level) Consultant & Director – Laboratory Services (MD Pathology, 12–15 y) Call & Whats app 8968364214

Medical Coding is the process of converting Verbal Descriptions into numeric or alpha numeric by using ICD 10-CM, CPT & HCPCS. As per HIPAA rules healthcare providers need efficient Medical Coders. Qualification & Specifications : MBBS, BDS, BHMS, BAMS, BSMS, PHARMACY B.Sc/M.Sc (Life Sciences / Biology / Bio Chemistry / Micro Biology / Nursing / Bio Technology), B.P.T, B.E BIOMEDIAL, B.Tech (Biotechnology/Bio Chemistry). 2020 -2024 passed out Skills Required: * Candidates should have Good Communication & Analytical Skills and should be Good at Medical Terminology (Physiology & Anatomy). Role: To review US medical records Initial file review for identifying merits Subjective review and analys...