Doc Review Spec I/ii

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

Biostatistician I / II - India - Office Based ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Biostatistician I to...

Assist in the processing of expedited safety reports (ESRs). This includes, but is not limited to: - maintenance of adverse event tracking systems. - set-up and maintenance of project files, core process files and central safety files. - assist with the reporting of ESRs to clients, regulatory authorities, ethics committees, investigators and Covance...

Assist in the processing of expedited safety reports (ESRs). This includes, but is not limited to: - maintenance of adverse event tracking systems. - set-up and maintenance of project files, core process files and central safety files. - assist with the reporting of ESRs to clients, regulatory authorities, ethics committees, investigators and Covance...

Position provides process, control, coordination, and approval of clinical trial documents. Position is responsible for ECD, Phase I-IV electronic trial master file (eTMF). - Maintains an understanding of applicable regulatory requirements. - Managing electronic Trial Master Files (eTMF), (Trial, Country and Site artifacts) for clinical studies in accordance...

**Business Unit**: Wonderla Resort, Bengaluru **Department**: F&B Production **Qualification**: B.H.M/Diploma or any degree/without degree **Experience**: 4-6 years (Only Male) **Report To**: HOD **Duties & Responsibilities**: As a Commis II, you are responsible for the daily food preparation and duties assigned to meet the set standard and qualities,...

**Job Overview**: Responsible for performing TMF review of electronic Trial Master Files (eTMF), Trial, Country, and Site artifacts for clinical studies in support of sponsors services contracts and internal Fortrea business needs. **Summary of Responsibilities**: - Position provides process, control, coordination, and approval of clinical trial...

Job Description Job Overview Provide basic and some comprehensive data management expertise to the Clinical Data Management (CDM) team to provide efficient, quality data management products that meet customer needs. May also undertake team leadership activities under the supervision of the Data Operations Coordinator (DOC), Data Team Lead (DTL), or...

Job Overview:Provide basic and some comprehensive data management expertise to the Clinical Data Management (CDM) team to provide efficient, quality data management products that meet customer needs. May also undertake team leadership activities under the supervision of the Data Operations Coordinator (DOC), Data Team Lead (DTL), or Functional...

Greetings from Netsach - A Cyber Security Company.We have an immediate requirement for Secure Code Review Consultant with yrs experience in Banking/BFSI domain.Job Title: Secure Code Review ConsultantExp: 6-12yrsJob Location: Bangalore Work Type: FulltimeInterested candidates please share your profile at and kindly register in and do share your...