Fresher Clinical Research executive-Reputed Clinical Industry-Hyderabad, Telangana, India-3LPA-Harshala

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 committee...

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 guidelines. 3....

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 guidelines. 3....

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 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 committee...

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 sites to...

JOB DETAILS 1. Prevent the payment of potentially fraudulent and/or abusive claims utilizing medical expertise, knowledge of CPT/diagnosis codes, CMC guideline along with referring to client specific guidelines and member policies2. Adhere to the state and federal compliance policies and contract compliance 3. Assist the prospective team with special...

JOB DETAILS 1) Professionally Counsel the Client on an online platform with the specified allocated slot.2) The potential callers are white collar employees of corporate undergoing stress and mental health issues due to personal and professional reasons and are expected to be counselled with primary active listening techniques and mindfulness practices. 3)...

JOB DETAILS 1) Professionally Counsel the Client on an online platform with the specified allocated slot.2) The potential callers are white collar employees of corporate undergoing stress and mental health issues due to personal and professional reasons and are expected to be counselled with primary active listening techniques and mindfulness practices. 3)...

Job description Support a PI sponsored Investigational New Drug (IND) or Investigational Device Exemption (IDE) Host/ prepare for external audits (sponsor, FDA, NIH, etc) Monitor or audit studies in the institution Facilitate and/or run research/project team meetings Prepare study budget Educate and mentor clinical staff, research team and other...