17 Patient Recruitment Jobs

Role Overview: As a Clinical Research Coordinator at Concept Clinical Service in Surat, your primary responsibility will be to coordinate clinical trials effectively. You will play a crucial role in obtaining informed consent from participants, ensuring adherence to study protocols, managing research documentation, and maintaining regulatory compliance. Your daily tasks will involve patient recruitment, data collection, monitoring activities, and facilitating communication within the study team and investigators. Key Responsibilities: - Coordinate clinical trials efficiently - Obtain informed consent from study participants - Adhere to study protocols and ensure compliance with regulatory re...

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 ...

As an Assistant in this role, you will assist in the coordination and conduct of clinical trials under supervision. Your key responsibilities will include: - Supporting patient recruitment, screening, and enrollment according to protocol criteria - Scheduling and managing patient visits, sample collection, and follow-ups - Collecting and accurately entering data into Case Report Forms (CRFs) or Electronic Data Capture (EDC) systems - Maintaining essential documents in the Investigator Site File (ISF) - Ensuring adherence to study protocols, ICH-GCP, and regulatory requirements - Assisting in the preparation for audits or monitoring visits - Communicating with sponsors, CROs, and ethics commi...

Company Description QREC Clinical Research LLP is a Contract Research Organization with offices in Jaipur (India), Hyderabad (India), and Dubai (UAE). We provide comprehensive services to the healthcare industry, including clinical trials (Phase 3 & 4), real-world studies, observational studies, PMS, KAP surveys, investigator-initiated studies, medical writing, clinical data management, statistical analysis, and medico-marketing globally. Our experience includes contributions to over 450 brand plans, 720+ medical writing projects, and numerous clinical data management and statistical analysis projects. QREC boasts a vast database, skilled manpower, and consistent audit success. Role Descript...

You will be responsible for monitoring patient data and study-related information at clinical study sites to ensure adherence to research protocols, regulatory requirements, and good clinical practices. Your role will involve providing input into data validation plans and ensuring timely and accurate monitoring of patient data. You may also be required to monitor study sites and audit facility selection. Key Responsibilities: - Act as the frontline liaison between Novartis and sites to ensure successful collaboration, meeting Novartis" expectations on milestones and deliverables with a true ownership mindset - Manage assigned study sites, conduct phase I-IV protocols according to the Monitor...

As the Medical Oversight for currently on-going projects, you will be responsible for participating in grant writing for all internal investigator initiated projects. Your role will also involve overseeing regulatory matters by periodically reviewing standard operating procedures, ensuring their enforcement, and updating as necessary. Additionally, you will be assisting with patient recruitment, data management, and statistical analysis. Furthermore, you will oversee administrative affairs to ensure smooth operations.,

Role Overview: As the Principal Investigator (PI) based in Noida, India, you will oversee the scientific, ethical, and regulatory aspects of clinical trials. Your crucial responsibilities include ensuring participant safety, protocol adherence, and data integrity throughout the trial process. Collaboration with sponsors, regulatory authorities, and internal teams will be essential to achieve successful trial outcomes. Key Responsibilities: - Serve as the lead medical expert for assigned clinical trials - Ensure compliance with ICH-GCP guidelines and local regulatory requirements - Oversee patient recruitment and informed consent processes - Document and report adverse events - Participate in...

As an experienced Life Sciences Subject Matter Expert (SME) with deep expertise across Commercial Analytics and R&D functions, you will play a crucial role in shaping solution strategies, evangelizing data-driven offerings, and driving innovation across the drug development and commercialization lifecycle. Your responsibilities will include: - **Commercial Analytics Strategy & Enablement**: - Evangelize advanced analytics solutions in areas such as sales & marketing effectiveness, patient journey analytics, market access, pricing & reimbursement, and digital engagement. - Guide biopharma and medtech clients on leveraging real-world data (RWD), claims, EMR, and patient registries to optimize ...

As a clinical research organization, Shree Clinical Services Pvt Ltd specializes in managing and conducting clinical trials across various therapeutic areas including oncology, cardiovascular diseases, and vaccines. The company is dedicated to ensuring compliance with Good Clinical Practice (GCP) guidelines to maintain high standards in the industry. Shree Clinical Services Pvt Ltd offers end-to-end clinical trial management services which include patient recruitment, regulatory documentation, and thorough data analysis. By leveraging their expertise and experience, the company aims to contribute significantly to the advancement of medical research and healthcare.,

As a Clinical Trial Coordinator, you will be responsible for overseeing the daily activities of clinical trials at various study sites. Your duties will include coordinating patient recruitment, screening, and assisting with the informed consent processes. Additionally, you will be tasked with maintaining trial documentation such as case report forms and regulatory binders. You will play a crucial role in scheduling and tracking study visits, as well as monitoring data collection and entry to ensure accuracy and compliance with protocols. Effective communication with investigators, sponsors, and ethics committees will be essential to the success of the trials. This is a full-time position th...

Job Responsibilities Safeguarding the wellbeing of research subjects in a medical capacity, ensuring that all procedures are conducted with the highest standards of care and safety Reviewing study protocols and executing procedures in alignment with protocols and regulatory, health, and safety standards, ensuring compliance with all relevant guidelines and regulations Recruiting and coordinating communication with clinical trial volunteers and patients, maintaining clear and effective communication throughout the study Following applicable regulations globally and by region, ensuring that all activities are conducted in accordance with local and international standards Collaborating with cro...

Job Responsibilities Safeguarding the wellbeing of research subjects in a medical capacity, ensuring that all procedures are conducted with the highest standards of care and safety Reviewing study protocols and executing procedures in alignment with protocols and regulatory, health, and safety standards, ensuring compliance with all relevant guidelines and regulations Recruiting and coordinating communication with clinical trial volunteers and patients, maintaining clear and effective communication throughout the study Following applicable regulations globally and by region, ensuring that all activities are conducted in accordance with local and international standards Collaborating with cro...

we're looking for a proactive and highly communicative clinical research professional, pivotal in critically analyzing and summarizing clinical literature to provide valuable insights Collaborating with cross-functional teams, you will contribute to the systematic review of medical literature, ensuring that our reports adhere to rigorous standards and regulatory guidelines Join us in our commitment to excellence within the realm of clinical research and literature analysis Department - Research & Analysis Skills Required - Data Validation Role Conduct systematic literature reviews (SLR) and meta-analyses, including screening and extraction. Prepare training data for AI model development. Wri...

We are seeking a motivated Trainee Clinical Research Associate (CRA) to join our team in India. This entry-level position offers an excellent opportunity to gain hands-on experience in clinical research, working alongside experienced professionals in the field. The ideal candidate will be passionate about advancing their career in clinical trials and contribute to the successful execution of research projects. Responsibilities Assist in the preparation and submission of regulatory documents. Support the planning and execution of clinical trials. Monitor study progress and ensure compliance with protocols and regulations. Assist in site selection and initiation visits. Collect and review data...

We are seeking an Assistant Clinical Research professional to join our team in India. The ideal candidate will support clinical trials and research studies, ensuring compliance with protocols and regulations. This role is suitable for candidates with 0-5 years of experience who are eager to contribute to clinical research. Responsibilities Assist in the design and implementation of clinical research studies. Maintain accurate records of study documentation and patient data. Coordinate with clinical trial sites and ensure compliance with protocols. Support the preparation and submission of regulatory documents. Assist in the collection and analysis of clinical trial data. Help in the training...

Description We are seeking an experienced Clinical Trials professional to manage and oversee clinical research studies in India. The ideal candidate will have a strong background in clinical trial design and execution, ensuring compliance with regulatory standards and the safety of trial participants. Responsibilities Design and implement clinical trial protocols in compliance with regulatory standards. Monitor trial progress and ensure adherence to timelines and budgets. Coordinate with various stakeholders, including sponsors, regulatory authorities, and clinical sites. Collect, analyze, and interpret data from clinical trials. Prepare and submit regulatory documents and reports. Train and...

Pharmabharat is a CRO based company specializing in clinical trials with a mission to support and accelerate clinical trials for innovative healthcare solutions. With a team of 11-50 employees, we are headquartered in Maharashtra and belong to the Hospitals and Health Care industry. We are currently looking for a highly motivated Clinical Research Associate to join our team. This full-time position is suitable for freshers with 0 to 1 year of work experience. The job locations include Pune, Bangalore Rural, Hyderabad, and Akrund. The ideal candidate will be responsible for overseeing and supporting clinical trials to ensure compliance with regulatory requirements. Qualifications and Skills: ...