3474 Clinical Trials Jobs - Page 28

Dear Candidate, CBCC Global Research is looking for CRA/Sr. CRA with oncology PK experience for Pune/Kolkata location. Job Code : CBCC/IND/CRA (Please mentioned job code in subject line of your application ) Work Experience: 3-8 Years Monitoring experience with Oncology PK studies is mandatory Work Location: Pune and Kolkata Pre-Requisite Skills: Minimum 2-3 years onsite monitoring experience mandatory Oncology Patient base PK studies monitoring experience is preferred Key Responsibilities Overall site management of clinical trials and Patient base PK studies Ensure effective communication to sites Prepare for site visits Assist PM in developing the project plan Prepare the Site Activation c...

Responsibilities: * Dispense medications accurately and efficiently * Collaborate with healthcare team on treatment plans * Provide patient counseling and education * Monitor drug interactions and adverse reactions

Description We are seeking a D- Pharmacist (Female) to join our team in India. This role involves providing pharmaceutical care, dispensing medications, and ensuring patient safety. The ideal candidate will have a strong foundation in pharmacy principles and a passion for patient care. Responsibilities Dispense medications and provide pharmaceutical care to patients. Ensure the safe and effective use of medications by providing counseling and education to patients. Maintain accurate records of prescriptions and patient interactions. Collaborate with healthcare professionals to optimize patient care. Monitor and manage inventory of medications and supplies. Stay updated on new medications and...

Responsible for regulatory activity related to clinical section for US, ;EU, WHO, Canada, Australia, New Zealand and South Africa Markets Preparation of bioequivalence related sections of ANDA product dossiers as per current regulatory guidelines Ensure timely preparation of amendments related to bioequivalence to expedite approvals Review of BE protocol for all market including ROW market Review of bio-waiver information and clinical strategy before start of clinical study. Confirmation of reference product for EU countries for clinical study Review and Preparation of 2.4 (non-clinical review) and 2.5 (clinical review) module for EU submissions Review of SmPC, PIL, Labeling for US, EU and o...

We are looking for a skilled finance professional with 10-18 years of experience to join our team as an Associate Director of Finance in the Hotels & Restaurants industry. Roles and Responsibility Oversee financial planning, budgeting, and forecasting to drive business growth. Develop and implement financial strategies to optimize profitability and minimize losses. Lead financial analysis and reporting to inform business decisions. Manage financial risk and ensure compliance with regulatory requirements. Collaborate with cross-functional teams to achieve business objectives. Provide financial guidance and support to senior management. Job Requirements Strong background in finance, accounting...

We are looking for a highly skilled and experienced Executive - HSEQ to join our team at GoKhana, with 1-3 years of experience in the field. 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 Requirem...

Role Overview: As a member of Shree Clinical Services Pvt Ltd, you will be part of a clinical research organization that specializes in managing and conducting clinical trials across various therapeutic areas like oncology, cardiovascular diseases, and vaccines. The company places a strong emphasis on ensuring compliance with Good Clinical Practice (GCP) guidelines. Your role will involve providing end-to-end clinical trial management, which includes tasks such as patient recruitment, regulatory documentation, and data analysis. Key Responsibilities: - Manage and conduct clinical trials in oncology, cardiovascular diseases, vaccines, and other therapeutic areas - Ensure compliance with Good ...

Job Title : Product Owner (Business Analyst) Location : Bangalore (Hybrid 2 days in office) Experience Required : Total : 7 Years & Relevant : 4 Years Notice Period : Immediate to 30 Days Work Timing : 7:30 AM to 5:30 PM IST Role Requirements 5+ years as a Product Owner or similar role Salesforce platform experience Requirements management using Jira Platform integrations (MuleSoft, Integration Fabric, APIs) Data flow understanding and data requirement management Responsibilities Translate product roadmap into actionable requirements Write detailed user stories and acceptance criteria Collaborate with developers and analysts Resolve conflicting user requirements Assist in process modelling a...

We are looking for a skilled Manager Admin to join our team in the hospitality industry. The ideal candidate will have 3-7 years of experience and be based in Saaki Argus & Averil Consulting. Roles and Responsibility Manage administrative tasks with precision and attention to detail. Coordinate with various departments to ensure smooth operations. Develop and implement effective administrative processes and procedures. Supervise and guide junior staff members. Maintain accurate records and reports. Ensure compliance with company policies and regulations. Job Requirements Proven experience in administration or a related field. Strong knowledge of administrative principles and practices. Excel...

As a Clinical Research Coordinator (CRC), you will assist in the planning, coordination, and execution of clinical trials at the site level. Required Candidate profile Assist the Principal Investigator in screening, recruiting, and enrolling study participants. Schedule subject visits and coordinate study-related procedures.

The Department: The Department Head and Neck Surgical Oncology at Tata Medical Center is an academic, multidisciplinary center dedicated to the diagnosis, treatment and research of head and neck cancer with infrastructure to perform complex ablative and reconstructive surgery, including microvascular reconstruction, in all types of head and cancer. Impart training in protocol based management of head and neck cancer in a multidisciplinary setting Introduce the trainee to basic and advanced surgical concepts and techniques of surgical oncology pertaining to the head and neck region Impart intensive training in reconstructive surgery towards the end of the fellowship with introduction to conce...

As a member of the LSGIU development organization, you will contribute to a mission-critical platform that enables our customers to develop solutions that address worldwide healthcare problems in therapeutic areas such as vaccines and oncology with unmatched performance, scale, and reliability. A successful candidate will be a strong team player who is able to work across multiple functions and disciplines. The candidate should be self-directed and have deep experience and knowledge of software design, coding, and testing methodologies. Architect, design, create, and maintain the full stack (front end and back end) of a customer-facing cloud-native application. Help create and review system ...

KnJ Projects Private Limited is looking for Material cum Quality Expert to join our dynamic team and embark on a rewarding career journey. Develop and implement quality assurance policies and procedures. Conduct quality audits and inspections. Analyze data to identify areas for improvement. Provide training on quality standards and processes. Ensure compliance with regulatory requirements. Disclaimer : This job description has been sourced from a public domain and may have been modified by Naukri. com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before applying.

- NISM 8 (Equity Derivative) must - Strong Understanding of stock market and Financial regulations. - Excellent Analytical and decision making skills - Ability to work under pressure and quick decisions. - MF certification is added advantage

E We are looking for a passionate and detail-oriented Regulatory Affairs Specialist (Fresher) to join our life sciences and healthcare compliance team. The ideal candidate will be responsible for assisting in the preparation, review, and submission of regulatory documents and ensuring adherence to national and international standards for product approval and compliance. This role offers a great opportunity for recent graduates in Pharmacy, Biotechnology, Life Sciences, or related fields to begin their career in the pharmaceutical and healthcare regulatory sector . Key Responsibilities: Assist in preparing and submitting regulatory documents to health authorities. Maintain up-to-date knowledg...

Help us bring cutting-edge medical treatments to life! Become a key player in clinical research and accelerate advancements in healthcare. Opportunities We offer two paths into the exciting world of clinical research: Internship: Get a hands-on introduction to clinical trials through a time-bound internship program. Ideal for students or recent graduates eager to experience the field. Fresher-Level Position: Launch your career as a Clinical Research Coordinator! This position offers ongoing employment for those committed to this exciting field. Regardless of path, you'll get to: Manage the flow of clinical trials: Oversee study logistics, participant documentation, and ensure the study progr...

The Clinical Data Coordinator (Intern/Fresher Level) plays a crucial role in ensuring the integrity and quality of clinical trial data. This position offers a valuable entry point into the field, providing hands-on experience in core data management tasks and industry best practices. Key Responsibilities: Data Entry and Verification: Meticulous data entry into electronic data capture (EDC) systems. Verify data accuracy and consistency against source documents (e.g., Case Report Forms). Learn to identify and flag potential data discrepancies. Query Generation and Resolution: Develop an understanding of data discrepancies and their underlying causes. Assist in generating data queries to clarif...

We are seeking a highly organized and detail-oriented Clinical Trial Coordinator (Fresher) to join our dynamic clinical research team. In this role, you will play a crucial part in ensuring the successful execution of our clinical trials from start to finish. You will collaborate with a multidisciplinary team of researchers, investigators, and study personnel to coordinate all aspects of clinical trial operations. Key Responsibilities: Study Coordination: Coordinate the day-to-day activities of assigned clinical trials, ensuring adherence to protocols, timelines, and regulatory requirements. Site Management: Assist in site selection, initiation, monitoring, and close-out activities. Document...

As a Clinical Project Manager, you will be responsible for overseeing clinical trials with a focus on interventional studies (Phase IIV). Your key responsibilities will include: - Directly managing and operationalizing clinical trial protocols into eSource/EDC workflows. - Managing end-to-end clinical trial processes such as start-up, site initiation, data collection, query management, and close-out. - Leading and mentoring CDM/clinical trial teams with a minimum of 5 years of people management experience. - Utilizing expertise in clinical trial systems like CTMS (CRIO preferred), eSource, and EDC platforms. - Working in pharmaceutical, biotechnology, or CRO environments across various thera...

JOB DESCRIPTION: Main Purpose of the Role Summarize the main purpose of the 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 List the main responsibilities this role regularly performs. 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 comple...

Senior CDC Bangalore/Chennai/Trivandrum, India Immediate Joiner ICON plc is a world-leading healthcare intelligence and clinical research organization Were 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 Senior Clinical Data Coordinator to join our diverse and dynamic team As a Clinical Data Coordinator at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of inNvative treatments and therapies, What You Will Be Doing Create and maintain detailed data m...

Clinical Trial Associate (Bangalore) ICON plc is a world-leading healthcare intelligence and clinical research organization Were 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 Clinical Trial Administrator to join our diverse and dynamic team As a Clinical Trial Administrator at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex medical data, and contributing to the advancement of inNvative treatments and therapies, What You Will Be Doing Assist in the coordination and administration...

IHCRA Bangalore ICON plc is a world-leading healthcare intelligence and clinical research organization Were 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 an IHCRA (In-House Clinical Research Associate) to join our diverse and dynamic team As an IHCRA at ICON, you will play a pivotal role in supporting the execution and management of clinical trials, contributing to the advancement of innovative treatments and therapies, What You Will Be Doing Performs a variety of routine essential document collection, review, negotiation, to ensure successful site ...

IHCRA Bangalore ICON plc is a world-leading healthcare intelligence and clinical research organization Were 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 an IHCRA (In-House Clinical Research Associate) to join our diverse and dynamic team As an IHCRA at ICON, you will play a pivotal role in supporting the execution and management of clinical trials, contributing to the advancement of innovative treatments and therapies, What You Will Be Doing Performs a variety of routine essential document collection, review, negotiation, to ensure successful site ...

As an experienced professional individual contributor in the Medical Affairs Sub-Function, you will work under limited supervision and apply subject matter knowledge in the field of Medical Affairs. You should have the capacity to apply your skills and knowledge within the context of specific needs or requirements. Your main responsibilities will include: - Overseeing the direction, planning, execution, clinical trials/research, and data collection activities in the Medical Affairs Sub-Function. - Contributing to the implementation of clinical protocols and facilitating the completion of final reports. - Recruiting clinical investigators, negotiating study design and costs, and directing hum...