3474 Clinical Trials Jobs - Page 16

Educational Qualifications: MBBS+ MD in Community Medicine with 3 to 4 years of experience as an Assistant Professor in a reputed Medical College Role Requirements: Academic Teaching : Conduct regular UG and PG teaching sessions, including theory, practicals, tutorials, and field postings, as per NMC guidelines. Curriculum Implementation : Oversee and contribute to the development and effective implementation of competency-based medical education (CBME). Research Supervision : Guide PG dissertations and research projects; actively publish in indexed peer-reviewed journals as mandated by NMC. Assessment & Evaluation : Design, conduct, and evaluate internal assessments and university exams in ...

Qualifications: MBBS + MD/DNB in General Medicine with minimum 3 years of relevant experience as an Assistant Professor in a reupted medical college. Key Responsibilities: Provide consultation to patients to assess their health concerns and medical histories. Write comprehensive medical reports and maintain accurate patient records. Conduct specialized diagnostic tests and interpret results to support patient care. Formulate and recommend appropriate treatment plans for patients. Collaborate with a patient's primary physician to ensure coordinated care. Perform thorough patient consultations, including detailed physical examinations. Offer general pre- and post-operative care, ensuring patie...

Role Overview: You will lead and manage Data Management (DM) teams within a specific DM operational business unit. As the Director of Clinical Data Management at Amgen, you will set and drive forward the vision and strategy for DM as a member of the DM and Global Study Operations (GSO) Leadership Team. You will be responsible for overseeing a distinct DM operational unit, recruiting, managing, and developing staff, setting functional goals and objectives, and ensuring DM processes and systems meet regulatory and business requirements. Additionally, you will play a key role in providing a foundation for GSO success. Key Responsibilities: - Oversight of a distinct DM operational unit (e.g. the...

Job Title: Clinical Research Project Manager Location: Vile Parle / Thane Working Days: Monday to Saturday (6 days) Experience: 510 years (Oncology / Clinical Research preferred) Employment Type: Full-time About the Role: MOC Cancer Care & Research Centre is seeking an experienced Clinical Research Project Manager to oversee and manage clinical trials across multiple oncology phases (I–IV). The role involves end-to-end project management, regulatory coordination, team leadership, and ensuring full compliance with GCP and DCGI guidelines. Key Responsibilities: Clinical Trial Management Oversee the conduct of Phase I–IV oncology clinical trials, ensuring adherence to study protocols, timelines...

Collect, clean, and analyze structured and unstructured data from multiple sources. Design, train, and fine-tune Generative AI models (e. g. , GPT, Stable Diffusion, etc. ) for various applications. Develop and optimize data pipelines to preprocess and manage large datasets for AI/ML models. Partner with business stakeholders to understand requirements, translate them into data-driven solutions, and deliver measurable outcomes. Build scalable APIs and services to deploy AI models in real-world applications. Build data pipelines for model training, evaluation, and continual learning. Monitor model performance, address bias or hallucination issues, and improve output reliability. Stay current ...

Roles and Responsibility Develop and implement effective health, safety, and environmental management systems. Conduct regular audits and inspections to ensure compliance with regulatory requirements. Provide training and guidance on health, safety, and environmental procedures. Investigate incidents and accidents, and develop corrective actions plans. Collaborate with other departments to promote a culture of health, safety, and environmental awareness. Maintain accurate records and reports on health, safety, and environmental performance. Job Requirements Strong knowledge of health, safety, and environmental regulations and standards. Excellent communication and interpersonal skills. Abili...

Should have knowledge in clinical research studies Monitoring of Clinical studies conducted at various CROs located globally as per ICH/GCP, applicable regulatory requirements, protocols and SOPs. Perform Site visits (i.e. Site Selection Visit) Required Candidate profile Strong understanding of clinical trial processes and regulatory requirements. Excellent clinical assessment skills and a commitment to patient safety and ethical research practices.

Perform triage & intake of ICSR received daily in ARGUS databases Should have hands On Experience On ARGUS Safety Database Should Have hands on Experience on MEDDRA Applicants Should Complete Certification in Pharmacoviiglance Required Candidate profile B.Pharm / M.Pharm/Pharm D/Life sciences degree With Hands On Experience On Argus Safety Database and Med DRA coding, Argus, Narrative Writing, Triage

Job description Should have knowledge in clinical research studies Perform Site visits (i.e. Site Selection Visit, Site Initiation Visits, Site monitoring visits and site close-out visits) should have knowledge in ICH GCP Guidelines Required Candidate profile Strong understanding of clinical trial processes and regulatory requirements. Excellent clinical assessment skills and a commitment to patient safety and ethical research practices.

Walk-In Interview for Pharmacy Life Science Fresh Graduates For Medical Coding Non Certified Applicants should have good knowledge in Medical Coding Anatomy and Medical Terminology Required Candidate profile Candidates Should have good knowledge in Medical Coding ICD 10, Anatomy Medical terminology and CPT

Walk-In Interview for Pharmacy Life Sciences Biotechnology Biochem Chemistry Nursing MLT Fresh Graduates For Medical Coding Non Certified Freshers Applicants should have good knowledge in Medical Coding Anatomy and Medical Terminology Required Candidate profile Candidates Should have good knowledge in Medical Coding ICD 10, Anatomy Medical terminology and CPT Exposure to CPT-4, ICD-9, ICD-10, and HCPCS coding

Walk-In Interview for Pharmacy Life Sciences Biotechnology Biochem Chemistry Nursing MLT Fresh Graduates For Medical Coding Non Certified Freshers Applicants should have good knowledge in Medical Coding Anatomy and Medical Terminology Required Candidate profile Candidates Should have good knowledge in Medical Coding ICD 10, Anatomy Medical terminology and CPT Exposure to CPT-4, ICD-9, ICD-10, and HCPCS coding

We are currently hiring for DSA I role with a minimum of 3 to 5 years Of experience in Pharmacovigilance Perform triage & intake of ICSR received daily in ARGUS databases. Ensure data entry of ICSR in ARGUS Knowledge In Aggregate Reporting is Must Required Candidate profile Require 3 to 5 years of pharmacovigilance case processing experience. Responsible for coding events using MEDDRA Any Life Sciences(B pharm/M Pharm/ Pharm D, Life Sciences, Nursing, BDS, BPT)

Should have knowledge in clinical research studies Monitoring of Clinical studies conducted at various CROs located globally as per ICH/GCP, applicable regulatory requirements, protocols and SOPs. Perform Site visits (i.e. Site Selection Visit) Required Candidate profile Strong understanding of clinical trial processes and regulatory requirements. Excellent clinical assessment skills and a commitment to patient safety and ethical research practices.

We are currently hiring for DSA I role with a minimum of 1 year experience in Pharmacovigilance Perform triage & intake of ICSR received daily in ARGUS databases. Ensure data entry of ICSR in ARGUS Required Candidate profile A minimum of 1 year pharmacovigilance case processing experience. Responsible for coding events using MEDDRA Any Life Sciences(B pharm/M Pharm/ Pharm D, Life Sciences, Nursing, BDS, BPT) are Eligible

Coordinate and manage clinical trials from initiation to completion, ensuring compliance with regulatory guidelines and study protocols. Should have knowledge in Clinical Data Management EDC Edit Checks SAE Reconcillation Required Candidate profile Maintain study supplies, track data collection, and support data analysis, ensuring high-quality and ethical research practices throughout the study

Clin Infotech is offering the internship opportunity for BDS MDS Dental Graduates Should have Knowledge in Pharmacovigilance Should Have knowledge on Argus & MEDDRA Applicants Should Complete Certification in Pharmacovigilance Required Candidate profile B.Pharm / M.Pharm/Pharm D/Life sciences degree With Hands On Experience On Argus Safety Database and Med DRA coding, Argus, Narrative Writing, Triage

The Associate pharmacovigilance specialist performs pharmacovigilance services such as biomedical literature monitoring and assessing for adverse events reporting, indexing, and abstracting by using broad knowledge of scientific terms and medical terminology, drugs and therapeutic areas, and pharmacovigilance regulations. About You - Education, Experience, Skills Masters Degree in life Sciences, Health, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics etc.). Fresher / Upto 2 years of experience reviewing biomedical literature for adverse event reporting OR equivalent combination of education and experience (i.e., an information science degree with at le...

Duties and Responsibilities: Responsibilities involve a combination of execution and oversight, dependent on the sourcing model, to ensure deliverables and may include, but are not limited to, the following: Project Management Spearheads collaboration with internal study teams and vendors to ensure clinical trial delivery meets established timelines, budgets, and quality benchmarks. Provides strategic input on study feasibility and oversees operational activities of internal and external contributors. Identifies and proactively manages risks, balancing trade-offs between cost, deliverables, and quality. Manages scope of work (SOW) for CROs and Vendor Partners, ensuring alignment with contrac...

ROLE SUMMARY Pfizer s purpose is to deliver breakthroughs that change patients lives. Research and Development is at the heart of fulfilling Pfizer s purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world. Pfizer is seeking a highly skilled and motivated AI Engineer to join our advanced technology team. The successful candidate will be responsible for developing, implementing...

We are looking for a skilled Process Coach to join our team at Omega Healthcare Management Services Pvt. Ltd., responsible for coding and ensuring the quality of healthcare services. The ideal candidate will have a strong background in healthcare management and excellent coaching skills. Roles and Responsibility Develop and implement process improvements to increase efficiency and productivity. Collaborate with cross-functional teams to identify areas for improvement and implement changes. Provide training and support to staff on new processes and procedures. Monitor and analyze performance metrics to ensure compliance with industry standards. Identify and mitigate risks associated with proc...

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...

Join us as a Trade & Transaction Reporting Manager Well look to you to provide oversight on daily trade and transaction reporting processes, making sure that they adhere to the control framework and comply with regulatory obligations Youll provide input into regulatory reporting initiatives, through your expertise and knowledge of regulations, data analysis and issue remediation As a key member of our team, youll enjoy extensive collaboration and can expect great visibility for you and your work We're offering this role at vice president level What you'll do As a Trade & Transaction Reporting Manager, youll be operating a robust oversight model of trade and transaction submissions to support...

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Project Financial Support Specialist Accountability Supporting Activities Projects Creation • Coordinate with Business Development, Client Finance, Finance...

We are looking for an Associate STEM Content Analyst to join our CDDI Chemistry team in Chennai (India). This is an amazing opportunity to work on content analysis for our Cortellis Drug Discovery Intelligence (CDDI) product. The team consists of 17 members based across Chennai, Hyderabad, Bangalore and Barcelona (Spain) and this role reports to the Chemistry Team Manager. We have a great skill set in Chemistry, Pharamacology, Medicinal chemistry, Synthesis andcomplementary skill sets to address challenges in drug discovery, including new chemical drugs identification, curation of drugs and formulations. We would love to speak with you if you have an understanding of chemical drug products. ...