Synowledge PV Services India Pvt Ltd 

Bangalore, Karnataka

Company details

Industry:
IT - Software/Services
Number of workers:
50
Website:
http://www.synowledge.com/

Company Description

Founded in 2006, Synowledge specializes in providing drug safety, regulatory affairs and related IT services to small, mid, and large sized pharmaceutical, biotechnology and medical device companies. We are headquartered in Stamford CT, USA with operational facilities across the United Kingdom, Columbus, Ohio, and Bangalore, India. Our comprehensive outsourcing solutions combine the unique strengths of both onshore and offshore services to meet all of our clients’ pressing needs.

Synowledge PV Services India Pvt Ltd 

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job postings

  • Bioclinica is hiring Italian Language Experts/ translators with excellent professional experience (reading, writing & speaking) in translating from Italian to English and vice versa. Any graduation with professional qualification in Italian

  • YEARS OF EXPERIENCE: 2-5 years experience in PV EDUCATION: MBBS/MD (in any discipline) ESSENTIAL DUTIES AND RESPONSIBILITIES: As a Medical Reviewer Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports Determine regulatory reportability of cases obtained from clinical trials, spontaneous and solicited reports within assigned ...

  • YEARS OF EXPERIENCE: 2-5 years experience in PV EDUCATION: MBBS/MD (in any discipline) ESSENTIAL DUTIES AND RESPONSIBILITIES: As a Medical Reviewer Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports Determine regulatory reportability of cases obtained from clinical trials, spontaneous and solicited reports within assigned ...

  • YEARS OF EXPERIENCE: 2-5 years experience in PV EDUCATION: MBBS/MD (in any discipline) ESSENTIAL DUTIES AND RESPONSIBILITIES: As a Medical Reviewer Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports Determine regulatory reportability of cases obtained from clinical trials, spontaneous and solicited reports within assigned ...

  • Supervision and coordination of following activities: Lead and manage the project to comply with the SOW and SLAs. Supervise all project related activities. Single point of contact between the team and the client for smooth functioning of the project. Communicate between the management and the team. Record, maintain and track the metrics for both team members and project performance. Review and evaluate ...

  • Supervision and coordination of following activities: Lead and manage the project to comply with the SOW and SLAs. Supervise all project related activities. Single point of contact between the team and the client for smooth functioning of the project. Communicate between the management and the team. Record, maintain and track the metrics for both team members and project performance. Review and evaluate ...

  • Essential Duties and Responsibilities: As a Medical Reviewer Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports Determine regulatory reportability of cases obtained from clinical trials, spontaneous and solicited reports within assigned therapeutic team and across all products/sites, as necessary, and in a timely fashion ...

  • Essential Duties and Responsibilities: As a Medical Reviewer Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports Determine regulatory reportability of cases obtained from clinical trials, spontaneous and solicited reports within assigned therapeutic team and across all products/sites, as necessary, and in a timely fashion ...

  • Essential Duties and Responsibilities: As a Medical Reviewer Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports Determine regulatory reportability of cases obtained from clinical trials, spontaneous and solicited reports within assigned therapeutic team and across all products/sites, as necessary, and in a timely fashion ...

  • The Director- RA position is responsible for the entire Regulatory function in India. The Director- RA will act as the single point of contact for number of Bioclinica accounts that provides Regulatory services and solutions to client. The Director- RA will be responsible for acting as the point of contact between the Clients and the Bioclinica India delivery project team. He/She will manage all ...

  • The Director- RA position is responsible for the entire Regulatory function in India. The Director- RA will act as the single point of contact for number of Bioclinica accounts that provides Regulatory services and solutions to client. The Director- RA will be responsible for acting as the point of contact between the Clients and the Bioclinica India delivery project team. He/She will manage all ...

  • The Director- RA position is responsible for the entire Regulatory function in India. The Director- RA will act as the single point of contact for number of Bioclinica accounts that provides Regulatory services and solutions to client. The Director- RA will be responsible for acting as the point of contact between the Clients and the Bioclinica India delivery project team. He/She will manage all ...

  • Lead/Co Lead cross functional teams contributing to periodic safety reports in accordance with Global Pharmacovigilance and Risk Management (GPRM) business rules, standard operating procedures (SOPs), and global regulatory requirements. Support roles involved in creation of Aggregate Safety Reports (ASRs) (i.e. PSURs, PADER, DSURs, PBRERs, Addendum to Clinical Overviews, Addendum to PSURs, Summary Bridging Reports ...

  • Lead/Co Lead cross functional teams contributing to periodic safety reports in accordance with Global Pharmacovigilance and Risk Management (GPRM) business rules, standard operating procedures (SOPs), and global regulatory requirements. Support roles involved in creation of Aggregate Safety Reports (ASRs) (i.e. PSURs, PADER, DSURs, PBRERs, Addendum to Clinical Overviews, Addendum to PSURs, Summary Bridging Reports ...

  • Lead/Co Lead cross functional teams contributing to periodic safety reports in accordance with Global Pharmacovigilance and Risk Management (GPRM) business rules, standard operating procedures (SOPs), and global regulatory requirements. Support roles involved in creation of Aggregate Safety Reports (ASRs) (i.e. PSURs, PADER, DSURs, PBRERs, Addendum to Clinical Overviews, Addendum to PSURs, Summary Bridging Reports ...

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