Clinical Trials

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...

**Roles & Responsibilities** - Conduct audits of clinical trail study - Conduct operations as per SOP - Conduct vendor audits - Maintain Quality system for clinical trial unit - Maintain relevant documentation **Criteria** Minimum of **2-5 years of experience** in pharmaceutical industry **Salary**: ₹35,000.00 - ₹58,000.00 per month Application...

_**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...

**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,...

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...

**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...

**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**: -...

**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...

**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...

**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...

As a clinical research associate (CRA), you'll **run clinical trials to test drugs for their effectiveness, risks and benefits to ensure that they are safe for the intended use**. Pay: Up to ₹27,000.00 per month **Benefits**: - Health insurance - Provident Fund Schedule: - Day shift Supplemental Pay: - Yearly bonus Work Location: In person

**SUMMARY** A part of the Study Support team the Resaerch Associte is responsible for performing work in the following operational areas as directed. The items below are a list of all planned duties of this role. The implementation of these duties will be staged as appropriate. **STATUS**:Full time **LOCATION**: Mumbai - Hybrid **DEPARTMENT**: Study...

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...

**Responsibilities** - Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations - Serve as primary Sponsor contact for operational project-specific issues and study deliverables - Maintain in depth knowledge of protocol, therapeutic...

Writing clinical trial protocol - Preparing SOP for selection of patient - Site initializing - Monitoring progress of trial - Ethics Committee submission - Data Analysis - Report writing - Publication in Peer reviewed journals **Job Types**: Full-time, Contract Contract length: 60 months **Salary**: From ₹40,000.00 per month **Benefits**: - Flexible...

**Key Responsibilities**: - Plan and execute training sessions on specified modules. - Develop comprehensive training content and curricula related to clinical research, including Good Clinical Practice (GCP), regulatory requirements, and data management. - Create additional case studies, assignments, and test series for students. - Evaluate student...

We are seeking a motivated individual to join our team as a Clinical Research Coordinator. This entry-level position offers an exciting opportunity for individuals interested in launching their career in clinical research. As a Clinical Research Coordinator, you will be responsible for assisting in the coordination and management of clinical trials, ensuring...

_**Clinical Research Associate Duties and Responsibilities**_ A competent Clinical Research Associate should be able to perform various duties and responsibilities. Proper fulfillment of a Clinical Research Associate’s duties and responsibilities brings success to your company. Clinical Research Associates should assist in organizing and monitoring the...