QA - Clinical Trials

Clinical trials are the actual experimental studies in which human volunteers are included, after their consent, to test new treatments, instruments, Read More

As a Clinical Trial Assistant (CTA) at [Company Name], you will play a crucial role in supporting the successful execution of clinical trials. Working closely with the clinical operations team, you will provide administrative and operational assistance to ensure the smooth conduct of trials from initiation to closeout. **Key Responsibilities**: - Maintain...

**Company Overview**Anicalls (Pty) Ltd is a dynamic company that values statistical expertise in clinical trials.**Job Summary**We are seeking an experienced Clinical Trial Statistician to join our team. The ideal candidate will have strong analytical skills and knowledge of statistical principles underlying clinical trials.**Required Skills and...

**Mumbai or Vadodara, India (hybrid: 3 days office, 2 days home)**: **Salary: Competitive + Benefits + Bonus**: If you are an agile, committed, and innovative clinical trial professional, then we want to hear from you! Join us to help improve peoples’ lives and make healthcare better for everyone! **Why Pharmanovia?**: Pharmanovia is a dynamic,...

Job DescriptionThe Clinical Project Lead role at Savvy Search involves leading a team of professionals in the Medical Affairs Sub-Function. This includes supervising the direction, planning, execution, and data collection activities of clinical trials research.Responsibilities:Lead a team of professionals in the Medical Affairs Sub-Function.Supervise...

_**Responsibilities**_ **To administer, maintain and coordinate the logístical aspects of the clinical trials according to Good Clinical Practice (GCP) and Standard Operating Procedures (SOPs).** To liaise with study participants and/or the study team to book appointments, resolve disrupted appointment times, offer new appointments and re-arrange existing...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

**Job Description:**As a Clinical Sas Programmer, you will be responsible for designing and analyzing clinical trials, developing statistical programming solutions, and coordinating with project management teams. You will work closely with our team to ensure timely delivery of high-quality results.**Responsibilities:**Design and analyze Phase I to IV...

Role Requirements:BE BS MS or international equivalent experience in statistics computer science mathematics life sciences or related field with Ideally 2 years of work experience in a programming role preferably supporting clinical trials.Basic SAS experience within a Statistical Programming environment to develop and validate deliverables.Basic experience...

Clinical Trial Coordinator - Mumbai for Pharma Company **Qualification**: - A post-graduate in life sciences/PharmD - GCP trained and Certified **Required Skills**: - Thorough understanding of drug development process and expertise in NDCT rules & ICH-GCP/Indian GCP - Knowledge of clinical trial regulation of US FDA, EMEA, NDCT rules, ICMR guidelines. -...

**Compliance Monitoring** - Ensure that clinical trials and research activities comply with regulatory standards (FDA, GxP, ICH guidelines). - **Auditing** - Conduct audits of clinical trial data, processes, and documentation to ensure accuracy and adherence to protocols. - **Documentation Review** - Review study protocols, informed consent forms, and case...

Job Title: Clinical Trial Manager ((Cardiovascular, Renal & Metabolic Disease (CVRM)) Job Location: Navi Mumbai, Maharashtra, India Job Location Type: On-site Job Contract Type: Full-time Job Seniority Level: Lifelancer ( https://lifelancer.com ) is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities...

**Summary**: Internal Role Title: Clinical Data Scientist Location: Mumbai #LI-Hybrid About the Role: Clinical Data Scientist is responsible of using advanced data management tools and techniques, provide professional and lean execution of Data Management products and milestones with respect to cost, quality and timelines for all assigned trials within...

Vasta Bio-Informatics Private LimitedMaharashtraPosted On - 19 Sep 2024 - Required Experience - 1 - 3 Years Basic SectionNo. Of Openings 5 Grade C1B Designation CLINICAL RESEARCH ASSOCIATE Closing Date 16 Jan 2025 - OrganisationalCountry IN State MAHARASHTRA City NAVI MUMBAI Location Navi Mumbai-I - SkillsSkill CLINICAL...

**Site Monitoring**:Conducting regular visits to clinical trial sites to ensure study protocols are followed accurately, including patient recruitment, data collection, and informed consent procedures. - **Data Quality Assurance**:Reviewing and verifying clinical trial data for accuracy and completeness, identifying and resolving discrepancies, and...

**Title**:Team Member - Clinical Research**: - Date: Feb 17, 2025 - Location: Sun House - Corporate Office - Company: Sun Pharma Laboratories Ltd **YOUR TASKS AND RESPONSIBILITIES**: **CRO Managed Studies**: - Manage Contract Research Organization (CRO) for effective execution of interventional, non-interventional and epidemiological studies - Identify...

**Job Type - Fresher or Internship level** Clinical Research Associates manage clinical trials and studies pertaining to biotechnological and pharmaceutical products, drugs and procedures. A Clinical Research Associate, also known as a CRA, conducts research to ensure these products are safe. **Responsibilities**: **1. Assist in Protocol Development**: -...

**Job Type - Fresher or Internship level** Clinical Research Associates manage clinical trials and studies pertaining to biotechnological and pharmaceutical products, drugs and procedures. A Clinical Research Associate, also known as a CRA, conducts research to ensure these products are safe. **Responsibilities**: **1. Assist in Protocol Development**: -...

105,000 people reimagining medicine for more than 766 million people globally. To provide country clinical strategic guidance and feasibility assessment for GDD trials. - Your responsibilities include, but are not limited to- To provide clinical strategic and tactical leadership in the country to support GDD trials, clinical development plans which change...

We are seeking a motivated and detail-oriented Clinical Research Coordinator (CRC) to join our team. This entry-level role is ideal for freshers passionate about contributing to clinical research and advancing healthcare solutions. **Key Responsibilities**: - Assist in coordinating day-to-day activities of clinical trials. - Obtain informed consent from...