17 Informed Consent Jobs

Role Overview: As a Clinical Research Coordinator (CRC), you will be responsible for managing and coordinating the day-to-day operations of a clinical trial. This includes tasks such as recruiting and screening participants, obtaining informed consent, collecting and managing data, and ensuring compliance with study protocols and regulations. Additionally, you will act as a liaison with sponsors, investigators, and regulatory bodies, maintain meticulous records, and may perform basic clinical procedures. Key Responsibilities: - Manage and coordinate the day-to-day operations of a clinical trial - Recruit and screen participants - Obtain informed consent from participants - Collect and manage...

As a Clinical Research Coordinator based in Meerut, your role will involve managing and overseeing clinical trials, ensuring compliance with research protocols, and obtaining informed consent from participants. You will be responsible for monitoring and documenting clinical research activities, coordinating with research teams, and maintaining accurate records of all research data. Key Responsibilities: - Manage and oversee clinical trials - Ensure compliance with research protocols - Obtain informed consent from participants - Monitor and document clinical research activities - Coordinate with research teams - Maintain accurate and up-to-date records of research data Qualifications Required...

Role Overview: As a Senior Clinical Research Coordinator at the company, you will oversee the daily activities of clinical trials at the Nagpur location. Your main responsibilities will include coordinating and supervising the informed consent process, ensuring compliance with protocols, handling documentation and records, liaising with participants, researchers, and medical staff, maintaining trial-related information, and ensuring trials are conducted ethically and in compliance with regulatory standards. Key Responsibilities: - Coordinating and supervising the informed consent process - Ensuring compliance with protocols - Handling all documentation and records related to research - Liais...

As a Medical Officer at our company located in Sector 44C, Chandigarh, your role will involve the following key responsibilities: - Inform the concerned consultant promptly upon patient admission. - Conduct and document detailed history and physical examinations. - Formulate a differential diagnosis for each case. - Develop and document the initial plan of care following the labor room PROTOCOL book. - Modify the daily plan of care as necessary. - Write daily progress notes to track patient status. - Obtain and document informed consent from patients. - Perform preoperative work-ups for surgical cases. - Order and interpret appropriate investigations, including hemodynamic parameters in crit...

You will be responsible for overseeing the day-to-day operations of clinical research studies at Biospecimen Solutions Pvt Ltd. This includes tasks such as obtaining informed consent, adhering to protocols, managing research activities, and ensuring compliance with clinical trial regulations. Key Responsibilities: - Coordinate the day-to-day operations of clinical research studies - Obtain informed consent from study participants - Follow protocols outlined for each research study - Manage various research activities as required - Ensure compliance with all clinical trial regulations Qualifications Required: - Possess skills in informed consent and protocol management - Previous experience i...

As a potential candidate for the role, you will be responsible for developing and implementing strategies to identify and attract study participants through various channels. This includes community outreach, social media, and partnerships. You will distribute recruitment materials such as brochures and advertisements to promote clinical trial opportunities. Additionally, you will conduct phone interviews to assess volunteer eligibility based on study-specific inclusion/exclusion criteria. Your key responsibilities will include: - Scheduling and coordinating screening appointments for potential participants - Obtaining and verifying informed consent from participants - Maintaining accurate p...

Role Overview: As a Duty Doctor at Syngene, your core purpose will be to screen and maintain complete data of volunteers, perform general physical examinations to ensure their fitness for participation in studies, review various laboratory test results, coordinate with Central Laboratory for required tests, assist in enrolling eligible volunteers, monitor subjects during studies, counsel screen failed volunteers, perform vitals, and ensure compliance with study protocols. Additionally, you will be responsible for maintaining the ICU, communicating with hospitals, managing the volunteer database software, obtaining informed consent, coordinating study activities, and fulfilling other assigned...

In this role of CRA II/ Sr CRA I at Syneos Health based in Mumbai with a focus on Oncology, you will play a crucial part in overseeing and ensuring the integrity of clinical research studies by monitoring data and processes. Your responsibilities will include conducting site qualification, site initiation, interim monitoring, site management activities, and close-out visits. Additionally, you will be responsible for ensuring regulatory, ICH-GCP, and protocol compliance, as well as evaluating site performance and providing recommendations. You will also be involved in tasks such as assessing subject/patient safety, conducting source document review, and ensuring site compliance with electroni...

Site Name: Warsaw Rzymowskiego 53, Bengaluru Luxor North Tower Posted Date: Sep 17 2025 GSK's success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves feeling welcome, valued and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together. Job Purpose: The Director Process Management will be accountable fo...

Roles and Responsibilities: Participant Coordination & Recruitment Work under the guidance of the Investigator to assist with all study-related responsibilities Conduct and document the informed consent process Educate participants on study procedures, duration, risks, benefits, and compensation Assist in subject enrollment and assign screening codes Maintain follow-up communication with participants Study Conduct & Compliance Ensure strict adherence to GCP , Ethics Committee (EC) guidelines, and the approved protocol Follow the Schedule of Assessments in coordination with the study team Coordinate lab activities: sample collection, processing, packaging, and shipping Ensure subject well-bei...

The job involves providing clinical study start-up expertise and assisting the Lead CRA in preparing IRB submissions, including reviewing site-specific informed consent and assent forms. You will be responsible for tracking IRB submissions, collecting, reviewing, and processing essential documents, as well as identifying any issues that the site needs to address. Communicating updates needed to essential documents to the site is also an essential part of the role. Additionally, you will lead or support the setup and maintenance of the Trial Master File (TMF) and assist or participate in planning and conducting Investigators Meetings as necessary. This is a full-time position that offers the ...

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...

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 collaborativ...

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 b...

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. ...

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...

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 a...