Pharma Associate Safety Specialist Job Opening @ PPD

Pharma Associate Safety Specialist Job Opening @ PPD

PPD invites Postgraduate and Undergraduate B Pharma and M Pharma candidates for the post of Safety Specialist. Candidates who have experience in safety handling and management and are willing to work for this big firm may apply for this job post. Candidates can apply via online mode.

Job Title: Associate Safety Specialist

Location: Hyderabad, Telangana, India

Requisition ID: 161300

Eligibility: Minimum Required Education and Experience:Bachelor’s degree in Nursing, Medical Technology or Pharmacy with 2+ years of clinical experience OR Life Science degree with 2+ years of clinical experience and 1 year of pharmacovigilance experience or equivalent combination of education, training, and experience that provides the individual with the required knowledge, skills, and abilities to perform the job required Knowledge,

Skills and Abilities:

• General understanding of pathophysiology and the disease process detailed knowledge of relevant therapeutic areas as required for processing strong critical thinking and problem solving skillsGood oral and written communication skills including paraphrasing
• skillsGood command of English and ability to translate information into local language where required computer literate with the ability to work within multiple database previous exposure to Microsoft Office packages (including Outlook, Word, and Excel)Understanding the importance of and compliance with procedural documents and regulations ability to manage and prioritize a variety of tasks and meet strict deadlines with limited supervisionStrong attention to detail ability to maintain a positive and professional demeanor in challenging circumstancesAbility to work effectively within a team to attain a shared goal working ConditionsWork is performed in an office environment with exposure to electrical office equipment.
• Occasional drives to site locations with occasional travel both domestic and international.
• Physical DemandsFrequently stationary for 6-8 hours per day. Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists. Frequent mobility required. Occasional crouching, stooping, bending and twisting of upper body and neck.
• Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs. Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
• Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.
• Frequently interacts with others to obtain or relate information to diverse groups. Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Requires multiple periods of intense concentration.
• Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task. Regular and consistent attendance

Working Conditions and Environment:

Work is performed in an office environment with exposure to electrical office equipment daily exposure to high pressure and intense concentration daily interactions with clients/associates long, varied hours on occasion travel

Job Description:

• The Safety Specialist performs day-to-day adverse event reporting and subsequent Pharmacovigilance (PVG) activities performed within a highly regulated environment and driven by strict timelines. Pharmacovigilance activities include but are not limited to collection, monitoring, assessment, evaluation, research and tracking of safety information.

• Coordinates and performs adverse event data entry, coding and assessment of adverse events, case review, follow-up, tracking of reports, and regulatory reporting activities. Effectively collaborates with various parties such as: project team members, client contacts, investigators, and adverse event/ reporters, and third party vendors.

• May assist in the preparation of departmental and project-specific procedures and processes, prepare for and attend audits, kick-off and investigator meetings.

Apply Online