6 Informed Consent Jobs

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 document reviews, resolve queries, and ensure site compliance with electronic data capture requirements. Additionally, you may be involved in investigational product inventory, reconciliation, and storage reviews. Maintaining accurate documentation, such as confirmation letters, follow-up letters, and trip reports, will be part of your routine tasks. You will support subject recruitment and retention strategies, enter data into tracking systems, and manage site-level activities to meet project objectives within specified timelines. Your adaptability to changing priorities and ability to communicate effectively with study site personnel will be crucial for success in this role. As a Clinical Research Associate II, you will also participate in Investigator Meetings, sponsor meetings, and clinical training sessions. You will work towards audit readiness standards, prepare for audits, and ensure compliance with applicable regulatory requirements. Your knowledge of Good Clinical Practice guidelines and relevant regulations will guide your actions throughout the study lifecycle. To excel in this role, you should hold a Bachelor's degree or RN in a related field, have knowledge of ICH Guidelines and regulatory requirements, possess strong computer skills, and be willing to travel up to 75% of the time. Excellent communication skills, the ability to work collaboratively, and a commitment to maintaining high standards of quality and compliance are essential for success in this position. Join us at Syneos Health, where you will have the opportunity to make a meaningful impact on the lives of patients and contribute to the advancement of healthcare through innovative clinical research practices. Discover a rewarding career with a global organization that values diversity, inclusivity, and professional growth. Visit our website to learn more about Syneos Health and the exciting opportunities we offer.,

The Sr. Clinical Research Coordinator position at Shree Clinical Research in Belgaum is a full-time on-site role that involves overseeing clinical trials, managing protocols, and ensuring regulatory compliance. In this role, you will be responsible for obtaining informed consent, coordinating with investigators, sites, and patients, and ensuring the smooth execution of clinical research activities. To qualify for this position, you should have experience in Clinical Research and Clinical Trials, proficiency in handling Informed Consent, knowledge of Protocol and Research methodologies, strong organizational and communication skills, and the ability to work both independently and collaboratively. A Bachelor's degree in a relevant field like Life Sciences or equivalent experience is required. Familiarity with ICH GCP and SOPs is considered a plus. Shree Clinical Research focuses on conducting multi-centre, multi-geography clinical trials and aims to establish long-term partnerships with Sponsors, investigators, sites, and patients. Equipped with ICH GCP and SOPs, the company ensures that all clinical trial activities adhere to regulatory principles and guidelines, maintaining the highest standards of ethics to safeguard patient safety and confidentiality.,

As a Registrar in Kolkata, your main responsibilities will include informing the concerned consultant promptly upon patient admission, conducting and documenting history & physical examinations, formulating a differential diagnosis, and developing an initial plan of care in accordance with labor room PROTOCOL book guidelines. You will be expected to modify the daily plan of care as needed, write daily progress notes, and obtain and document informed consent from patients. Additionally, your role will involve performing preoperative work-ups, interpreting hemodynamic parameters in critically ill patients, interpreting laboratory and radiology results, ordering and overseeing transfusions of blood and blood products, ordering appropriate investigations and medications, and preparing discharge summaries while explaining post-discharge instructions to patients. It will also be your responsibility to write the duty report in the duty register, receive and provide written handovers and takeovers daily, and complete insurance forms to be signed by the concerned consultant. Furthermore, you will be required to perform pelvic examinations, Pap smears, cardio-pulmonary resuscitation, nasogastric intubation, urethral catheter insertions, and order and adjust artificial feeding modalities as necessary. Candidates for this position are expected to hold an MBBS degree along with MD, DNB, or DGO qualifications and have 0-4 years of relevant experience. This is a full-time role that demands attention to detail, strong communication skills, and the ability to work effectively within a medical team.,

You will be joining Q-Max Clinical Research Services as a Clinical Research Coordinator at their Nadiad location. Your primary responsibilities will include managing tasks related to informed consent, protocol management, research coordination, and supporting clinical trials. To excel in this role, you should possess skills in informed consent and protocol management, along with previous experience in clinical research and coordinating clinical trials. Attention to detail and strong organizational skills are crucial for success in this position. Additionally, effective communication, excellent interpersonal skills, and the ability to work collaboratively in a team environment are essential. Ideal candidates for this role will hold a Bachelor's or Master's degree in a relevant field such as Life Sciences or Health Sciences. Certification in Clinical Research would be considered a valuable advantage. If you are seeking a challenging opportunity to contribute to successful drug development outcomes and work in a dynamic environment, this role at Q-Max Clinical Research Services may be the perfect fit for you.,

As a Manager of Clinical Research at Teva Pharmaceuticals, you will play a crucial role in ensuring the proper conduct of studies related to BA/BE Studies. Your responsibilities will include complying with all applicable regulations, completing necessary forms, and adhering to the GCP, EC/Sponsor agreed protocol, Lotus SOPs, regulatory requirements, and ethical principles. Before the study starts, you will review and provide timely inputs on the protocol, obtain ethics committee approval, and ensure that all study personnel are trained and aware of their obligations. You will be overall responsible for supervising study-related activities, providing timely inputs in the protocol and Informed Consent, and submitting required study documents to the Ethics Committee for approval. Additionally, you will coordinate screening activities in clinical centers, screen volunteers for clinical studies, and decide on subject eligibility based on various parameters. Maintaining accurate records of screening procedures, counseling subjects, and referring them to appropriate facilities when necessary will also be part of your responsibilities. To qualify for this role, you should hold an MBBS or MD degree and have at least 10 years of experience in BA/BE Studies. By joining Teva Pharmaceuticals, you will be part of a global mission to make good health more affordable and accessible, impacting millions of lives worldwide. If you are passionate about making a difference in healthcare and meet the qualifications for this position, we encourage you to apply now and be a part of our team dedicated to improving the lives of others.,

You will be responsible for performing and documenting history & physical examination, formulating a differential diagnosis, developing and documenting the initial plan of care, modifying daily plan of care, writing daily progress notes, obtaining and documenting informed consent, ordering appropriate referrals and investigations, interpreting hemodynamic parameters in critically ill patients, interpreting laboratory & radiology results, ordering transfusions of blood and blood products, ordering appropriate medication and other necessary orders, and preparing an appropriate discharge summary. In terms of administrative duties, you will be required to perform cardio-pulmonary resuscitation and actively participate in teaching and academic activities both intradepartmentally and interdepartmentally. Your role will also involve clinical invasive management which includes administering General & Regional anaesthesia and appropriate interventions. This is a full-time position with health insurance benefits and a fixed shift schedule. The ideal candidate should have a Bachelor's degree (Preferred) and a minimum of 1 year of experience as a Physician (Preferred) with a total of 1 year of work experience. The work location for this position is in person.,