Safety & Pv Coordinator (Hyderabad)

**Description**

**Safety & Pharmacovigilance Coordinator**

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.

Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.

Discover what our 29,000 employees, across 110 countries already know:
**WORK HERE MATTERS EVERYWHERE**

**Why Syneos Health**
- We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
- We are committed to our Total Self culture - where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
- We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives - we're able to create a place where everyone feels like they belong.

**Job responsibilities**
- Monitors and routes incoming information to the appropriate project if required.
- Records all ICSR documentation and tracks in accordance with Sponsor/customer specifications; distributes incoming mail and faxes if required.
- Redacts patient identifying information/ images in accordance with data protection guidelines, ICH GCP and GVP if required.
- Enters data into the safety database in accordance with Sponsor/customer specific guidelines and Company standards if required.
- Ensures current conventions are followed when entering cases into the Safety database.
- May perform file creation, tracking, retention, and maintenance (paper and electronic).
- Manages the translation process for any source documents requiring translation if required.
- Performs or assist with query follow up process as instructed.
- Assists with submission processes as required.
- Assists with daily workflow reconciliation.
- Assists with literature screening and review for safety, drug coding, maintenance of drug dictionary, MedDRA coding, if required.
- Assists with narrative writing.
- Assists with coding events, medical history, concomitant medications, and tests.
- Assists in the generation of timely, consistent, and accurate reporting of expedited reports in accordance with applicable regulatory requirements.
- Validation of xEVMPD product records, including appropriate coding of indication terms using MedDRA, if required.
- Manual recoding of un-recoded product and substance terms arising from ICSRs if required.
- Identification and management of duplicate ICSRs if required.
- Activities related to SPOR / IDMP if required.
- Ensures all relevant documents are submitted to the Trial Master File (TMF) as per company SOP/Sponsor requirements for clinical trials and the Pharmacovigilance System Master File for post-marketing programs as appropriate.
- Maintains understanding of Standard Operating Procedures (SOPs), Work Instructions (WIs), global drug/biologic/device regulations, GCP, ICH guidelines, Good Pharmacovigilance Practice (GVP) modules, study/program plans and the drug development process.
- Fosters constructive and professional working relationships with all project team members, internal and external.
- Participates in audits as required/appropriate.
- Applies safety reporting regulatory intelligence maintained by Syneos Health to all safety reporting activities.

**Qualifications**

**What we're looking for**
- Bachelor's Degree in life science, registered nurse, pharmacist 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 and medical terminology preferred.
- 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

**Get to know Syneos Health**
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

No matter what your role is, you'll take the initiative