49 Clinical Protocols Jobs - Page 2

Role Overview: Tap Health is a deep tech startup focused on helping individuals manage chronic conditions through AI-first, mobile-first digital therapeutics. As a Freelance Diabetes Consultant / Doctor, you will play a key role in shaping the diabetes care protocols for Tap Health's fully autonomous AI-driven diabetes therapeutic. This freelance role allows you to work remotely and you will be compensated based on the hours delivered. Key Responsibilities: - Co-create and review protocol logic for onboarding, triage, glucose feedback, medications, lifestyle, and follow-ups. - Translate guidelines into clear decision flows, state machines, and safety guardrails. - Define red flags, escalatio...

As the Lead Clinical Operations at a Digital Health Company based in Mumbai, your role will involve overseeing and managing the clinical operations of the cardiac rehabilitation program. You will be responsible for developing and implementing clinical protocols and guidelines in line with best practices to ensure high-quality patient care and adherence to clinical standards. Your key responsibilities will include: - Leading, mentoring, and training a multidisciplinary team of health professionals, including Dieticians, Care Managers, and Mental Wellness experts. - Conducting regular performance reviews and providing continuous professional development opportunities for the team. - Fostering ...

Role Overview: As a Global Trial Manager, Clinical Operations at Sun Pharma, you will play a crucial role in the clinical development team based in Mumbai. Reporting to the Global Trial Leader, Clinical Operations, you will be responsible for assisting in the management of Sun Pharmaceuticals clinical trials globally, regionally, or at the complex local level. Your primary focus will be on overseeing the end-to-end clinical trial management process, including start-up, execution, close-out, and finalization of study reports. Your contributions will be essential in ensuring that all project tasks and timelines are on track. Key Responsibilities: - Oversight of CRO / other vendors and study ma...

Contact Mr Manoj Thenua WhatsApp 63986528 32 Job Title: Interventional Radiology Consultant (DM/DNB/MD) Location: Ajmer, Rajasthan Job Description We are seeking an experienced Interventional Radiology Consultant to join our advanced healthcare team in Ajmer, Rajasthan. The ideal candidate will be responsible for performing minimally invasive image-guided procedures, providing expert diagnosis, and delivering high-quality patient care. Key Responsibilities Perform interventional radiology procedures including angiography, embolization, biopsies, stent placements, drainage procedures, and other image-guided interventions. Interpret radiological images and provide accurate diagnostic reports. ...

Job Description Head, Emergency Department Location: NCR Region (Delhi/NCR) Position: Head of Emergency Department Qualification (Mandatory): MD in Emergency Medicine / General Medicine / Anesthesia Role Overview: We are seeking an experienced and dynamic medical professional to lead and manage the Emergency Department at our NCR facility. The Head of Emergency will be responsible for ensuring high standards of patient care, clinical governance, and operational efficiency within the department. The role requires both clinical expertise and strong leadership to guide a multidisciplinary emergency team. Key Responsibilities: Provide overall leadership and supervision to the Emergency Departmen...

Role Overview: You will work as an experienced professional individual contributor in the area of Medical Affairs with limited supervision. Your role will involve applying subject matter knowledge to meet specific needs or requirements. Key Responsibilities: - Possess well-developed skills in overseeing direction, planning, execution, clinical trials/research, and data collection activities in the Medical Affairs Sub-Function. - Contribute to the implementation of clinical protocols and facilitate the completion of final reports. - Recruit clinical investigators, negotiate study design and costs. - Direct human clinical trials, phases III & IV for company products under development. - Partic...

As a Quality Assurance Specialist in a healthcare setting, your primary responsibility will be to implement and monitor Quality Management Systems in accordance with NABH 6th Edition standards. This includes conducting internal audits, gap assessments, and compliance checks to ensure adherence to quality and accreditation requirements. You will take the lead in driving quality improvement and patient safety initiatives across various departments within the organization. In this role, you will be tasked with developing, reviewing, and updating policies, SOPs, and clinical protocols to maintain high-quality standards. Additionally, you will be responsible for training and mentoring staff on qu...

JOB DESCRIPTION: Specialist professional individual contributor with comprehensive knowledge in the area of Medical Affairs. Ability to execute highly complex or specialized projects. Adapts precedent and may make significant departures from traditional approaches to develop solutions. . As the Specialist in the Medical Affairs Sub-Function, considered as highly experienced and knowledgeable resource within the organization in overseeing the direction, planning, execution, clinical trials/research and the data collection activities. . Contributes to implementation of clinical protocols, and facilitates completion of final reports. . Recruits clinical investigators and negotiates study design...

You will be the Senior Medical Officer - Intensive Care Unit (ICU) at Unique Hospital in Delhi, Dwarka. In this role, you will play a crucial part in providing advanced medical care to critically ill patients who require intensive monitoring and comprehensive management. Your responsibilities will include overseeing and managing the day-to-day operations of the ICU department, conducting patient rounds, examinations, and assessments, as well as developing and implementing treatment plans for ICU patients. Additionally, you will be responsible for supervising and supporting the medical staff and interdisciplinary team members, participating in the development and implementation of clinical pr...

We are looking for a dedicated and skilled M.D. Physician / M.D. Medicine to join our full-time medical team. The ideal candidate will be responsible for diagnosing, treating, and managing patients with a wide range of medical conditions. Key Responsibilities: Provide comprehensive medical care to patients across all age groups. Diagnose illnesses, prescribe medication, and monitor treatment outcomes. Collaborate with other specialists and medical staff for integrated patient care. Maintain accurate and up-to-date patient records. Participate in medical audits, reviews, and case discussions. Ensure adherence to clinical protocols and hospital standards. Candidate Requirements: Qualification:...

****If interested then kindly apply on below link**** https://noccarc.notion.site/clinicalresearcherspecialist About Role: As a Clinical Research Specialist at Noccarc, you will be the in-house doctor who brings the ICU to our R&D floor. You will shape next-generation critical care devices by defining clinical requirements, guiding product development, driving validation and trials, benchmarking against global standards, and leading medical writing and research that advance both our products and the field of critical care. To know more about Noccarc visit: www.noccarc.com Noccarc office video: https://youtu.be/OoeD10ckrdU Role: Clinical Research Specialist Location: Pune (5 days WFO) Reporti...

As a Regional Submission Manager - Sponsor-dedicated with CTIS experience at Syneos Health, you will play a crucial role in driving regional submission management strategy and activities for assigned protocols. You will collaborate with major functional areas, including SSU and Study Management, regarding essential core documents and local documentation needed from relevant supplier lines across both HA and EC submission and translation processes. Your responsibilities will include partnering with study teams to manage required regulatory activities, standards, and deliverables associated with CTA submission development. You will be responsible for authoring Annex I and completing relative a...

As a healthcare professional at InfoWryt Solutions LLP, you will play a crucial role in improving patient care and offering innovative solutions in the medical field. Your primary responsibility will be to conduct thorough patient assessments and examinations, diagnose urological conditions, and formulate effective treatment plans. Additionally, you will be involved in performing urological surgeries, providing post-operative care, and collaborating with multidisciplinary teams to ensure comprehensive patient management. Your role will also include educating patients on pre-operative and post-operative care, maintaining accurate patient records, and staying updated with the latest advancemen...

As a Clinical Coach (Quality Improvement), you will be responsible for supporting the district quality team and the project team in enhancing the clinical competencies and skills of facility clinical and managerial staff. Your role will involve coaching and mentoring healthcare professionals in applying quality improvement methodologies to improve clinical processes and patient outcomes. Moreover, you will be instrumental in devising clinical protocols, procedures, standards, and specifications to work towards achieving National Quality Assurance Certification for health facilities. Your key duties and responsibilities will include collaborating with clinical staff to assess current practice...

As a Site Activation Specialist II at Syneos Health, you will be responsible for ensuring quality deliverables at the country level while following project requirements and applicable country rules under moderate oversight from the SSU Country Manager. You will work within forecasted submission/approval timelines, track milestone progress in the SSU tracking system, and investigate any delays with clear rationale and contingency plans as needed. Additionally, you will monitor basic financial aspects of the project, review and comply with Standard Operating Procedures (SOPs) and Work Instructions (WI), and support the continuous improvement of quality in all Site Start-Up (SSU) components. Yo...

Perform maintenance of company SOPs in compliance with ICH-GCP, international and national regulations Review, approval and archival of company SOPs in compliance with ICH-GCP, international and national regulations Review and maintain company archives of clinical protocols and study documents Conduct QA internal audits of all aspects of the Clinical Research Departments activities to ensure compliance with ICH-GCP and applicable international and company procedures Perform QA reviews of protocols and other documents and data in preparation for submission to IRB/IEC, regulatory health authorities and publications Provide training to research staff on GCP, ICH and local regulations (as requir...

JOB DESCRIPTION: MAIN PURPOSE OF 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 .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 completion of final reports. .Recruits clinical investigators and negotiates study design and costs. .Respon...

Basic HealthCare Services (BHS) is a not-for-profit organization located in Udaipur, Rajasthan, dedicated to building a responsive and empathetic "circle of care" within the community. The vision of BHS is to empower marginalized and vulnerable communities to lead a healthy life with dignity. The organization's mission is to deliver high-quality, affordable primary healthcare services to communities in southern Rajasthan. BHS has established a network of "AMRIT Clinics" that provide a wide range of preventive, promotive, and curative healthcare services. These services are supplemented by focused interventions targeting maternal and child health, tuberculosis, chronic respiratory diseases, m...

The intensivist consultant plays a crucial role in providing specialized care to critically ill patients in the intensive care unit. As a key member of the healthcare team, you will be responsible for delivering high-quality, evidence-based care to patients with complex and life-threatening conditions. Collaboration with multidisciplinary teams to assess, diagnose, and manage patients is essential to ensure optimal outcomes and patient safety. Your key responsibilities will include assessing and managing critically ill patients in the intensive care unit, developing and implementing comprehensive treatment plans, utilizing advanced monitoring and life support equipment, performing invasive p...

TruVita Wellness Inc. is an innovative health-tech startup dedicated to revolutionizing healthcare through the integration of AI-powered telemedicine and personalized patient engagement tools. The platform is designed to enhance accessibility, efficiency, and empathy in primary care services. Key components of the platform include the AI Doctor (Avatar), telemedicine booths, continuous health monitoring, and a comprehensive wellness ecosystem offering round-the-clock access and data-driven insights. As a Medical Doctor with an entrepreneurial mindset, you have the opportunity to join TruVita Wellness as a Co-Founder. This role is ideal for a physician who is enthusiastic about leveraging tec...

The main purpose of your role as an experienced professional individual contributor in Medical Affairs is to work under limited supervision and apply your subject matter knowledge effectively. Your capacity to apply skills and knowledge should meet specific needs or requirements within the field. As an experienced professional in the Medical Affairs Sub-Function, you will be responsible for overseeing the direction, planning, and execution of clinical trials and research activities. You will play a key role in data collection, implementation of clinical protocols, and ensuring completion of final reports. Additionally, you will be involved in recruiting clinical investigators, negotiating st...

As a Pediatric Hematologist Consultant, you will be responsible for providing specialized medical care to pediatric patients with blood disorders. Your role will involve diagnosing and treating various hematologic conditions, collaborating with multidisciplinary teams, and contributing to pediatric hematology research. You will be expected to provide comprehensive care to pediatric patients with hematologic disorders through thorough clinical evaluations and diagnostic assessments. Developing personalized treatment plans and collaborating with other specialists to address complex cases will be crucial aspects of your responsibilities. Additionally, your involvement in clinical research, acad...

Job Title : Manager Quality Assurance Department : Quality Assurance Reporting to : Assistant General Manager Quality Assurance Location : Akhand Jyoti Eye Hospital (Centre of Excellence) with regular visits to all satellite centres Purpose of the Role : To champion, sustain and continuously improve the Quality Management System (QMS) across the hospital network, assuring patient safety, regulatory compliance, and an all pervasive culture of excellence. Consolidated Job Description Sr. No.Broad Responsibility AreaKey Job Descriptions (JD)1Quality Management System (QMS) & Documentation Control Own the QMS and ensure alignment with NABH / ISO standards Maintain the master list of documents, S...

Perform maintenance of company SOPs in compliance with ICH-GCP, international and national regulations Review, approval and archival of company SOPs in compliance with ICH-GCP, international and national regulations Review and maintain company archives of clinical protocols and study documents Conduct QA internal audits of all aspects of the Clinical Research Departments activities to ensure compliance with ICH-GCP and applicable international and company procedures Perform QA reviews of protocols and other documents and data in preparation for submission to IRB/IEC, regulatory health authorities and publications Provide training to research staff on GCP, ICH and local regulations (as requir...