Syneos Health B Pharma & M Pharma Job


Syneos Health B Pharma & M Pharma Job Vacancy - Safety & PV Coordinator

Syneos Health B Pharma & M Pharma Job – Safety & PV Coordinator

Syneos Health Life hiring Safety & PV Coordinator. Pharma Safety & PV Coordinator job opening 2022. B Pharma & M Pharma job opening 2022. Safety & PV Coordinator job opening 2022. Candidates with bachelor’s degree and master’s degree in pharmacy may apply for the job vacancy at Syneos. Check out all the details on the same below:

Job Title: Safety & PV Coordinator – For Gurgaon Location Applicants only

Location: India-Asia Pacific – IND-Gurugram-Cyber-City, India

Job ID: 22007705

Qualifications

What they are looking for

• B.pharms, M.Pharms, BDS or an equivalent combination of education and experience that gives the individual the necessary knowledge, skills and abilities to perform the job.

• Safety Database systems, additional course in Pharmacovigilance and medical terminology preferred.

• Proficiency in Microsoft Office Suite (Word, Excel and PowerPoint), Visio, email (Outlook), TeamShare (or other management/shared content/workspace) and internet.

• Works with others as part of a team

• Ability to successfully prioritize and work on multiple tasks

• Excellent communication and interpersonal skills, both written and spoken

• Strong organizational and documentation skills

• Detailed oriented with a high degree of accuracy

Job Responsibilities

• Monitors and routes incoming information to the appropriate project

• Records all ICSR documentation and tracks in accordance with Sponsor/customer specifications; distributes incoming mail and faxes.

• Redacts patient identifying information/ images in accordance with data protection guidelines, ICH GCP and GVP.

• Enters data into the safety database in accordance with Sponsor/customer-specific guidelines and Company standards.

• Ensures current conventions are followed when entering cases into the Safety database.

• Performs file creation, tracking, retention, and maintenance (paper and electronic).

• Manages the translation process for any source documents requiring translation.

• Performs or assist with query follow up process as instructed

• Assists with submission processes as required

• Assists with daily workflow reconciliation

• Maintains an understanding of Standard Operating Procedures (SOPs), Work Instructions (WIs), global drug/biologic/device regulations, GCPs, ICH guidelines, Good Pharmacovigilance Practice (GVP) modules, study/program plans and the drug development process.

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