19 Clinical Practice Jobs

Manage patient vital records. Manage patients through the course of the treatment; monitor daily patient condition and communicate any discrepancies or flags to the treating physician. Adjust and administer patient medication as per the guidelines of the physician and administer IV. Supervise patient treatment while making him/her comfortable throughout the patient stay in the hospital. Ensure cleanliness and hygiene for safe and comfortable treatment. Interested candidate may apply or walk in for interview at the hospital between 10:30AM to 4:30PM or contact 9350104290 for more information.

Job Description: A Senior Lecturer in prosthodontics is responsible for teaching undergraduate and postgraduate dental students, guiding clinical practice, conducting research, and contributing to departmental administration. The role involves delivering lectures, supervising patient care in the clinic, and advancing academic excellence in the field of prosthodontics. Roles and Responsibilities : The Senior Lecturer in prosthodontics imparts theoretical and clinical knowledge in subjects such as complete dentures, removable and fixed partial dentures, implant prosthodontics, and maxillofacial prosthetics. They deliver lectures, lead seminars, and supervise preclinical and clinical training, ensuring students gain hands-on experience in patient care. The role involves preparing academic materials, conducting internal assessments, mentoring students, and promoting ethical and evidence-based dental practice. The lecturer also engages in research activities, contributes to academic publications, and participates in national and international conferences. Additionally, they support departmental development, assist in curriculum design, maintain clinical records, and uphold quality standards in both teaching and patient care.

Manage patient vital records Manage patients through the course of the treatment; monitor daily patient condition and communicate any discrepancies or flags to the treating physician Adjust and administer patient medication as per the guidelines of the physician and administer IV Supervise patient treatment while making him/her comfortable throughout the patient stay in the hospital Ensure cleanliness and hygiene for safe and comfortable treatment

We are seeking a motivated and detail-oriented Clinical Research Associate (Fresher) to join our clinical research team. You will assist in the planning, monitoring, and documentation of clinical trials while ensuring compliance with regulatory guidelines and study protocols. Key Responsibilities: Assist in the coordination and monitoring of clinical trials across various sites. Ensure accurate collection, documentation, and reporting of clinical data. Support investigators and site staff with study protocols and procedures. Verify compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines. Help in preparing study-related documents and reports. Participate in site visits, audits, and data review activities. Assist in conducting clinical trials and analyzing research data.

We are seeking a motivated and detail-oriented Clinical Research Associate (Fresher) to join our clinical research team. You will assist in the planning, monitoring, and documentation of clinical trials while ensuring compliance with regulatory guidelines and study protocols. Key Responsibilities: Assist in the coordination and monitoring of clinical trials across various sites. Ensure accurate collection, documentation, and reporting of clinical data. Support investigators and site staff with study protocols and procedures. Verify compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines. Help in preparing study-related documents and reports. Participate in site visits, audits, and data review activities. Assist in conducting clinical trials and analyzing research data.

We are seeking a motivated and detail-oriented Clinical Research Associate (Fresher) to join our clinical research team. You will assist in the planning, monitoring, and documentation of clinical trials while ensuring compliance with regulatory guidelines and study protocols. Key Responsibilities: Assist in the coordination and monitoring of clinical trials across various sites. Ensure accurate collection, documentation, and reporting of clinical data. Support investigators and site staff with study protocols and procedures. Verify compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines. Help in preparing study-related documents and reports. Participate in site visits, audits, and data review activities. Assist in conducting clinical trials and analyzing research data.

We are seeking a motivated and detail-oriented Clinical Research Associate (Fresher) to join our clinical research team. You will assist in the planning, monitoring, and documentation of clinical trials while ensuring compliance with regulatory guidelines and study protocols. Key Responsibilities: Assist in the coordination and monitoring of clinical trials across various sites. Ensure accurate collection, documentation, and reporting of clinical data. Support investigators and site staff with study protocols and procedures. Verify compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines. Help in preparing study-related documents and reports. Participate in site visits, audits, and data review activities. Assist in conducting clinical trials and analyzing research data.

We are seeking a motivated and detail-oriented Clinical Research Associate (Fresher) to join our clinical research team. You will assist in the planning, monitoring, and documentation of clinical trials while ensuring compliance with regulatory guidelines and study protocols. Key Responsibilities: Assist in the coordination and monitoring of clinical trials across various sites. Ensure accurate collection, documentation, and reporting of clinical data. Support investigators and site staff with study protocols and procedures. Verify compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines. Help in preparing study-related documents and reports. Participate in site visits, audits, and data review activities. Assist in conducting clinical trials and analyzing research data.

We are seeking a motivated and detail-oriented Clinical Research Associate (Fresher) to join our clinical research team. You will assist in the planning, monitoring, and documentation of clinical trials while ensuring compliance with regulatory guidelines and study protocols. Key Responsibilities: Assist in the coordination and monitoring of clinical trials across various sites. Ensure accurate collection, documentation, and reporting of clinical data. Support investigators and site staff with study protocols and procedures. Verify compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines. Help in preparing study-related documents and reports. Participate in site visits, audits, and data review activities. Assist in conducting clinical trials and analyzing research data.

We are seeking a motivated and detail-oriented Clinical Research Associate (Fresher) to join our clinical research team. You will assist in the planning, monitoring, and documentation of clinical trials while ensuring compliance with regulatory guidelines and study protocols. Key Responsibilities: Assist in the coordination and monitoring of clinical trials across various sites. Ensure accurate collection, documentation, and reporting of clinical data. Support investigators and site staff with study protocols and procedures. Verify compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines. Help in preparing study-related documents and reports. Participate in site visits, audits, and data review activities. Assist in conducting clinical trials and analyzing research data.

We are seeking a motivated and detail-oriented Clinical Research Associate (Fresher) to join our clinical research team. You will assist in the planning, monitoring, and documentation of clinical trials while ensuring compliance with regulatory guidelines and study protocols. Key Responsibilities: Assist in the coordination and monitoring of clinical trials across various sites. Ensure accurate collection, documentation, and reporting of clinical data. Support investigators and site staff with study protocols and procedures. Verify compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines. Help in preparing study-related documents and reports. Participate in site visits, audits, and data review activities. Assist in conducting clinical trials and analyzing research data.

We are seeking a motivated and detail-oriented Clinical Research Associate (Fresher) to join our clinical research team. You will assist in the planning, monitoring, and documentation of clinical trials while ensuring compliance with regulatory guidelines and study protocols. Key Responsibilities: Assist in the coordination and monitoring of clinical trials across various sites. Ensure accurate collection, documentation, and reporting of clinical data. Support investigators and site staff with study protocols and procedures. Verify compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines. Help in preparing study-related documents and reports. Participate in site visits, audits, and data review activities. Assist in conducting clinical trials and analyzing research data.

We are seeking a motivated and detail-oriented Clinical Research Associate (Fresher) to join our clinical research team. You will assist in the planning, monitoring, and documentation of clinical trials while ensuring compliance with regulatory guidelines and study protocols. Key Responsibilities: Assist in the coordination and monitoring of clinical trials across various sites. Ensure accurate collection, documentation, and reporting of clinical data. Support investigators and site staff with study protocols and procedures. Verify compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines. Help in preparing study-related documents and reports. Participate in site visits, audits, and data review activities. Assist in conducting clinical trials and analyzing research data.

We are seeking a motivated and detail-oriented Clinical Research Associate (Fresher) to join our clinical research team. You will assist in the planning, monitoring, and documentation of clinical trials while ensuring compliance with regulatory guidelines and study protocols. Key Responsibilities: Assist in the coordination and monitoring of clinical trials across various sites. Ensure accurate collection, documentation, and reporting of clinical data. Support investigators and site staff with study protocols and procedures. Verify compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines. Help in preparing study-related documents and reports. Participate in site visits, audits, and data review activities. Assist in conducting clinical trials and analyzing research data.

We are seeking a motivated and detail-oriented Clinical Research Associate (Fresher) to join our clinical research team. You will assist in the planning, monitoring, and documentation of clinical trials while ensuring compliance with regulatory guidelines and study protocols. Key Responsibilities: Assist in the coordination and monitoring of clinical trials across various sites. Ensure accurate collection, documentation, and reporting of clinical data. Support investigators and site staff with study protocols and procedures. Verify compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines. Help in preparing study-related documents and reports. Participate in site visits, audits, and data review activities. Assist in conducting clinical trials and analyzing research data.

We are seeking a motivated and detail-oriented Clinical Research Associate (Fresher) to join our clinical research team. You will assist in the planning, monitoring, and documentation of clinical trials while ensuring compliance with regulatory guidelines and study protocols. Key Responsibilities: Assist in the coordination and monitoring of clinical trials across various sites. Ensure accurate collection, documentation, and reporting of clinical data. Support investigators and site staff with study protocols and procedures. Verify compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines. Help in preparing study-related documents and reports. Participate in site visits, audits, and data review activities. Assist in conducting clinical trials and analyzing research data.

We are seeking a motivated and detail-oriented Clinical Research Associate (Fresher) to join our clinical research team. You will assist in the planning, monitoring, and documentation of clinical trials while ensuring compliance with regulatory guidelines and study protocols. Key Responsibilities: Assist in the coordination and monitoring of clinical trials across various sites. Ensure accurate collection, documentation, and reporting of clinical data. Support investigators and site staff with study protocols and procedures. Verify compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines. Help in preparing study-related documents and reports. Participate in site visits, audits, and data review activities. Assist in conducting clinical trials and analyzing research data.

We are seeking a motivated and detail-oriented Clinical Research Associate (Fresher) to join our clinical research team. You will assist in the planning, monitoring, and documentation of clinical trials while ensuring compliance with regulatory guidelines and study protocols. Key Responsibilities: Assist in the coordination and monitoring of clinical trials across various sites. Ensure accurate collection, documentation, and reporting of clinical data. Support investigators and site staff with study protocols and procedures. Verify compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines. Help in preparing study-related documents and reports. Participate in site visits, audits, and data review activities. Assist in conducting clinical trials and analyzing research data.

We are seeking a motivated and detail-oriented Clinical Research Associate (Fresher) to join our clinical research team. You will assist in the planning, monitoring, and documentation of clinical trials while ensuring compliance with regulatory guidelines and study protocols. Key Responsibilities: Assist in the coordination and monitoring of clinical trials across various sites. Ensure accurate collection, documentation, and reporting of clinical data. Support investigators and site staff with study protocols and procedures. Verify compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines. Help in preparing study-related documents and reports. Participate in site visits, audits, and data review activities. Assist in conducting clinical trials and analyzing research data.