67 Clinical Monitoring Jobs - Page 2

Premier Research is looking for a Medical Specialist to join our Medical Affairs team. You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success. We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires. Your ideas influence the way we work, and your voice matters here. As an essential part of our team, you help us deliver the medical innovation that patients...

Major accountabilities: Provides medical support to Clinical Program Leader (CPL) leading the program. Medical support may include, but is not limited to, contributing to clinical sections of protocols and/or amendments, Informed Consents, publications, regulatory documents such as Investigator Brochures, responses to Health Authority questions and conducting ongoing review of clinical trial data, with oversight of TCO deliverables. May act as the medical monitor to support overall program safety reporting (e.g., Drug Safety Update Reports (DSURs), and other safety related documents) in collaboration with Patient Safety Team. May represents CPL at project team meetings (e.g. CTT) and may pro...

As a Clin Ops Specialist/CTA based in Athens, your role at Syneos Health will involve performing activities in compliance with applicable Corporate and Clinical Operations Policies, Standard Operating Procedures, and Work Instructions. You will assist Clinical Monitoring staff with site management activities, serving as a Sponsor representative for assigned studies and ensuring compliance with protocol requirements and relevant guidelines by communicating with sites. Additionally, you will create and assist with maintenance of Trial Master File (TMF) and project files, participate in file audits, prepare site manuals and other documents, update clinical tracking information databases, and tr...

As a Sr CRA I based in Beijing at Syneos Health, you will play a crucial role in monitoring clinical research studies to ensure they are conducted in line with established clinical practices. You will be responsible for both on-site and remote monitoring, developing tools, procedures, and processes to maintain quality monitoring standards. Your dedication to contributing to the design, implementation, and delivery of processes and programs will be instrumental in the success of clinical research studies. Syneos Health is committed to fostering a supportive and engaging work environment where career development, progression, and peer recognition are prioritized. As part of our Total Self cult...

As a Clinical Research Associate II (Sponsor dedicated) in Athens Homebase at Syneos Health, you will play a crucial role in ensuring site compliance with regulatory guidelines and protocol requirements. Your responsibilities will include performing site qualification, initiation, monitoring, management activities, and close-out visits either on-site or remotely. You will assess site performance, provide recommendations, and escalate any serious issues to the project team promptly. Your attention to detail will be essential as you verify the informed consent process, assess factors affecting subject safety, and review clinical data for accuracy and completeness. You will conduct source docum...

At EY, you'll have the chance to build a career as unique as you are, with the global scale, support, inclusive culture, and technology to become the best version of you. And we're counting on your unique voice and perspective to help EY become even better, too. Join us and build an exceptional experience for yourself, and a better working world for all. We are seeking a dynamic Manager to join our Life Sciences Consulting team, specializing in Clinical Operations transformation. This role involves working with global pharmaceutical, biotech, and medtech clients to optimize R&D and clinical delivery models, streamline operations, and implement emerging technologies across clinical developmen...

At Allucent, we are dedicated to assisting small-medium biopharmaceutical companies in efficiently navigating the complex world of clinical trials to bring life-changing therapies to patients in need globally. We are currently seeking a Sr. Clinical Research Associate Contractor (SrCRA) to join our A-team on a remote basis for 0.5Fte. As a SrCRA Contractor at Allucent, you will be responsible for independently controlling and monitoring investigational sites, proactively identifying issues, and providing solutions to ensure that clinical studies are conducted according to the trial protocol and in compliance with SOPs, relevant regulations, and the principles of Good Clinical Practice. Your ...

The GCP Compliance Manager (GCO) is responsible for overseeing and controlling compliance of regulated GCO activities, focusing on those with a high impact on GCO's ability to meet objectives. This role plays a crucial part in supporting GCP Compliance pillars, including issue management, audits, and inspections, particularly system/process audits and global inspections for authorizations and GCO self-strategy delivery. As the GCP Compliance Manager (GCO), you will provide GxP expertise and support GCP Compliance for various functions, compliance, process, training, and risk groups. Your responsibilities will include managing systemic quality issues, deviations, quality events, audits, and i...

As a Senior Clinical Operations Specialist (Senior CTA) in the Hybrid model in Athens at Syneos Health, you will play a crucial role in ensuring compliance with Corporate and Clinical Operations Policies, Standard Operating Procedures, and Work Instructions. Your responsibilities will include assisting Clinical Monitoring staff with site management activities, maintaining project files, handling project correspondence, participating in file audits, and preparing and maintaining site manuals and reference tools. Additionally, you will be responsible for updating clinical tracking information into databases, tracking documents, managing the shared mailbox, and coordinating site supplies and ma...

Role & responsibilities Participate in the investigator recruitment process. Perform initial qualification visits of potential investigators and sites. Evaluate the capability of the site to successfully manage and conduct the clinical study, both clinically and technically. Work with the Study Start-up Group to coordinate activities with the site in preparation for the initiation of studies. Obtain regulatory documentation for successful implementation, monitoring, and evaluation of clinical trials. Perform study initiation activities, reviewing with the site study team the protocol, regulatory issues, study procedures, and provide training on completion of the e-CRF; monitoring activities ...

- Successfully complete our internal training plan to include hemodynamics, ECG, angiography, echo CT imaging modalities and complete the case support and proctor delegate authorizations. - Provide active commercial case support, demonstrating excellence in procedural success rates patient outcomes. - Scrub in sterile and provide TAVI valve loading in procedures training instruction to trial and commercial customers - Provide our customers CT valve sizing analysis utilizing the Pie Medical 3Mensio CT program - Lead customer didactic education sessions for account activation before first implants - Lead pre case planning debriefing of heart team pre post procedure and provide ongoing educatio...

Minimum Qualifications BA or BS degree Experience in CRO or Pharmaceutical industry Ability to prioritize activities effectively to accomplish individual and team goals with competing deadlines Ability to write and speak clearly and concisely in a variety of communication settings and styles Strong interpersonal skills; ability to establish and promote positive business relationships; customer service oriented Ability to collaborate with study staff and internal and external partners to achieve goals Proficient computer skills including use of MS Office Suite (Word, Excel, PowerPoint) and enterprise clinical trial management systems Strong organizational skills and attention to detail Strong...

Clinical Trial Associate (CTA) provides essential administrative and operational support to clinical trial teams, assisting with tasks related to document management, regulatory compliance, communication, and data management. CTAs play a crucial role in ensuring trials are conducted efficiently and ethically, and in accordance with established guidelines. Here's a more detailed breakdown: Key Responsibilities: Document Management: CTAs are responsible for creating, collecting, organizing, and maintaining essential study documents, including protocols, informed consent forms, case report forms, and study plans. Regulatory Compliance: They ensure all trial-related activities adhere to relevant...

The clinical operations activities at our organization are expanding rapidly, and we are currently looking for a full-time Clinical Research (CRA) Manager to join our Clinical Monitoring team in Navi Mumbai, India. In this role, you will play a crucial part in the clinical trial management process at Medpace. If you are seeking a challenging career where you can utilize your existing expertise and further develop and advance your professional journey, then this opportunity is perfect for you. Your responsibilities will include: - Managing a team of Clinical Research Associates (CRAs) - Recruiting, providing initial and ongoing training, and fostering the development of CRAs - Overseeing and ...

The Associate Medical Expert in Translational Clinical Oncology (TCO) plays a crucial role as the medical leader for various global studies, roll-over studies, long-term follow-up studies, and studies in the close-out phase. Working under the guidance of a Clinical Program Leader (CPL) and/or Medical Expert, you will provide essential medical support for assigned aspects of active TCO studies. TCO is a department within the Biomedical Research division that focuses on designing and conducting early phase clinical studies in cancer patients, aiming to develop innovative treatments for oncology conditions and bridge the gap between drug discovery and late-phase clinical development. In this ro...

As a Clinical Research (CRA) Manager at Medpace, you will play a crucial role in the clinical trial management process within our growing clinical operations team in Navi Mumbai, India. Your responsibilities will include line management of Clinical Research Associates (CRAs), overseeing recruitment, training, and development of CRAs, ensuring CRAs meet core monitoring responsibilities, managing CRA resourcing and allocation, as well as addressing turnover and retention to align with company objectives. To excel in this role, you should hold a Bachelor's degree with 4-6 years of experience in the pharmaceutical industry, specifically in clinical monitoring or study management. Ideally, you sh...

Key Responsibilities Design, plan, and oversee clinical trials from initiation to closeout Develop study protocols, informed consent forms, and case report forms Ensure compliance with GCP, ICH, and local regulatory guidelines Manage trial budgets, timelines, and resources Coordinate with CROs, investigators, and ethics committees Monitor trial progress and resolve operational issues Review and analyze clinical data for accuracy and integrity Prepare reports and presentations for internal and external stakeholders Train and mentor clinical research staff Support regulatory submissions and audits Qualifications & Skills M.Pharm / M.Sc / MBBS / MD in Life Sciences, Pharmacy, or Medicine 8-12 y...

Key Responsibilities 1. Clinical Oversight Ensure adherence to treatment protocols and SOPs across all units. Monitor clinical indicators, patient outcomes, and audit reports. Guide units on medico-legal processes, compliance, and NABH standards. Review critical incident reports and follow up on action taken. Provide clinical direction during health emergencies or outbreaks. 2. Administrative Coordination Supervise hospital operations remotely through MIS, dashboards, and unit-level coordination. Support policy implementation and resolve escalated clinical-operational issues. Standardize workflows across departments in consultation with Unit Heads. Facilitate inter-unit coordination to maint...

Role Responsibilities: Deliver full-spectrum nursing care in clinical settings. Support physicians during medical procedures and surgeries. Monitor vital signs and patient responses to treatments. Maintain precise and up-to-date patient records. Job Requirements: Graduate or postgraduate in nursing. Experience in hospital or surgical environments. Strong clinical and observational skills. Ability to work collaboratively in a multidisciplinary team.

The Medical Expert in TCO (Translational Clinical Oncology) serves as the medical leader for assigned global, roll-over, and long-term follow-up studies, as well as studies in the close-out phase. Additionally, they may provide medical co-leadership for assigned aspects of global, active TCO studies under the guidance of a Clinical Program Leader (CPL). TCO, a department under the Biomedical Research division, is responsible for designing and conducting early-phase clinical studies in cancer patients, acting as a connection between drug discovery and late-phase clinical development to deliver innovative medicines for oncology conditions. Responsibilities include providing medical support to ...

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at Job Function: R&D Operations Job Sub Function: Clinical Trial Support Job Category: Professional All Job Posting Locations: Mumbai, India, PENJERLA, Telangana, India Job Description: A Senior, ...

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at Job Function: R&D Operations Job Sub Function: Clinical Trial Project Management Job Category: Professional All Job Posting Locations: Mumbai, India Job Description: A Senior, Local Trial Manag...

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at Job Function: R&D Operations Job Sub Function: Clinical Trial Project Management Job Category: Professional All Job Posting Locations: IN004 Bangalore, IN022 Hyderabad, Mumbai, India Job Descri...

Designation: Duty Medical Officer Location: Ranchi Qualification: MBBS; ACLS and VLS certification Experience: 0-1 years Other Requirements: • Proven expertise in new patient assessments, dialysis session monitoring, and emergency consultations. • Experience in ordering investigations and ensuring accurate medication administration. • Proficient in entering details into online portals, strong analytical skills, and effective English communication. • MS Office basic is essential. Interested candidates can send their resume to: Contact Number: 6291037010 / harpreet.gill@nephroplus.com

Hi , We have Opening for Clinical research Coordinator Location : Guwahati Salary : 23k take-home interested candidate Kindly drop your updated resume to below mail id Nithya_kumar@persolkelly.com Regards, Nithya CONFIDENTIAL NOTE: By submitting your resume or personal data, you acknowledge reading and agreeing to our Privacy Policy. You hereby provide voluntary consent to the collection, use, processing, and disclosure of your data by us and our affiliates, in line with the Privacy Policy. and applicable laws. If you wish to withdraw your consent or have any concerns, you may submit a request to our designated consent manager, as outlined in our Privacy Policy. We prioritize your privacy. S...