Jobs For Clinical Investigation Manager-Reputed Clinical Industry-Hyderabad, Telangana, India-7 Lakhs-Vishal

JOB DETAILS 1. Responsible for performing activities in compliance with applicable Corporate and Clinical Operations Policies, Standard Operating Procedures and Work Instructions2. Assists Clinical Monitoring staff with site management activities, including serving as a Sponsor representative for sites on assigned studies, and communicating with...

JOB DETAILS 1. Responsible for performing activities in compliance with applicable Corporate and Clinical Operations Policies, Standard Operating Procedures and Work Instructions2. Assists Clinical Monitoring staff with site management activities, including serving as a Sponsor representative for sites on assigned studies, and communicating with...

JOB DETAILS 1. Ensure that clinical research studies are conducted in accordance with the protocol, standard operating procedures, good clinical practice (GCP) guidelines, and other applicable regulatory requirements.2. Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and GCP...

JOB DETAILS 1. Ensure that clinical research studies are conducted in accordance with the protocol, standard operating procedures, good clinical practice (GCP) guidelines, and other applicable regulatory requirements.2. Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and GCP...

JOB DETAILS 1. To assess the new patients when they come first time to the clinic2. To take detailed history and physically examine the patient3. To complete patient history form, visit patient and review medical record. Obtain relevant clinical information4. To review as needed and discuss problems with consultant5. To be an in-house consultant for...

JOB DETAILS 1. To assess the new patients when they come first time to the clinic2. To take detailed history and physically examine the patient3. To complete patient history form, visit patient and review medical record. Obtain relevant clinical information4. To review as needed and discuss problems with consultant5. To be an in-house consultant for...

JOB DETAILS 1 Develop and maintain in-depth knowledge for assigned product(s) / relevant therapeutic area(s) through attendance/ participation at key internal meetings/training sessions, relevant congresses, and seminars and by regular self-study of the national/international literature.2 Provide expert medical/scientific advice for assigned...

JOB DETAILS1) Creating and writing trial protocols, and presenting these to steering committee.2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial.3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion.4) Liaise with ethics committee...

JOB DETAILS 1) Creating and writing trial protocols, and presenting these to steering committee.2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial.3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion.4) Liaise with ethics...

JOB DETAILS 1) Creating and writing trial protocols, and presenting these to steering committee.2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial.3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion.4) Liaise with ethics...

**Title**: Clinical Programmer **Department**: Engineering Support the organization’s mission, vision, and values by exhibiting the following behaviors: excellence and competence, collaboration, innovation, respect, commitment to our community, and accountability and ownership. Job SummaryPrimary responsibilities are clinical programming and data...

JOB DETAILS 1) Creating and writing trial protocols, and presenting these to steering committee.2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial.3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion.4) Liaise with ethics...

JOB DETAILS 1) Creating and writing trial protocols, and presenting these to steering committee.2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial.3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion.4) Liaise with ethics...

JOB DETAILS 1) Performing the Case Analysis and Peer Review (Quality check)2) Perform medical review (including verifying the coding & labeling, reviewing narratives, causality statement, medical aspect of follow-up request), validate follow-up request and perform medical assessment of the case for the Category I and II cases3) Prioritize workloads...

JOB DETAILS 1) Evaluate health message scripts and content for clinical accuracy.2) Check documents (mentioned above) developed by copywriters for clinical and scientific, reporting errors by checking the developed material against annotated references, clinical guidelines, other published sources data3) Check for discrepancy within different...

JOB DETAILS 1.Generating new business leads & taking care of the existing clients.2.Meeting up with doctors, nursing homes & various hospitals for glucometer sales & getting prescriptions.3.Actively participating in the special activities conducted by the doctors.4.Develop and maintain in-depth knowledge for assigned products relevant therapeutic...

JOB DETAILS 1.Generating new business leads & taking care of the existing clients.2.Meeting up with doctors, nursing homes & various hospitals for glucometer sales & getting prescriptions.3.Actively participating in the special activities conducted by the doctors.4.Develop and maintain in-depth knowledge for assigned products relevant therapeutic...

JOB DETAILS 1)Leading R&D efforts of company from its inception to develop a range of protein-based medicine.2)Building and implementing a detailed biochemical laboratory research work plan to fulfill company's research objectives3)Working to improve and expand company's novel protein cross linking formulation4)Developing prototypes for range of...

JOB DETAILS 1)Leading R&D efforts of company from its inception to develop a range of protein-based medicine.2)Building and implementing a detailed biochemical laboratory research work plan to fulfill company's research objectives3)Working to improve and expand company's novel protein cross linking formulation4)Developing prototypes for range of...

Eligibility: - Graduate / Post Graduates in Life Sciences/ Pharmacy from a reputed institute - Prior knowledge of the conduct of Clinical Trials, - Phases of Clinical trials and - Thorough Knowledge of ICH-GCP and other regulatory guidelines. Roles and Responsibilities: - Prepare the Database of the Investigators at the place assigned to you. - Interact...