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Internship (Pharmacovigilance) - Remote

Freshers years
Not Disclosed
10 Feb. 16, 2024
Job Description
Job Type: Full Time Education: Any Graduate Skills: Communication Skills, Interpersonal Skill, Technical Skill

About the job

EVERSANA is the leading independent provider of global services to the life science industry. The company’s integrated solutions are rooted in the patient experience and span all stages of the product lifecycle to deliver long-term, sustainable value for patients, prescribers, channel partners and payers. The company serves more than 500 organizations, including innovative start-ups and established pharmaceutical companies to advance life science services for a healthier world. To learn more about EVERSANA, visit eversana.com or connect through LinkedIn and Twitter.

Necessary trainings and mentorship will be provided for the role. Top performers will be considered favorably for future permanent positions if/when they arise.

OUR CULTURAL BELIEFS

  • Patient Minded: I act with the patient’s best interest in mind.
  • Client Delight: I own every client experience and its impact on results.
  • Take Action: I am empowered and empower others to act now.
  • Grow Talent: I own my development and invest in the development of others.
  • Win Together: I passionately connect with anyone, anywhere, anytime to achieve results.
  • Communication Matters: I speak up to create transparent, thoughtful and timely dialogue.
  • Own It: I hold myself and others accountable for results.
  • Embrace Diversity We create an environment of awareness and respect

 

THE POSITION:

§ We are seeking a motivated and detail-oriented Pharmacovigilance Intern to join our dynamic team. This internship provides an excellent opportunity for individuals interested in the pharmaceutical industry and drug safety to gain hands-on experience in Pharmacovigilance activities.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Our employees are tasked with delivering excellent business results through the efforts of their teams. These results are best achieved by:

§ Assist in the collection and documentation of adverse event reports from various sources.

§ Input data into the pharmacovigilance database accurately and in a timely manner.

§ Conduct literature searches to identify relevant safety information and adverse events associated with our products.

§ Summarize and present findings to the Pharmacovigilance team.

§ Assist in the quality control of pharmacovigilance data, ensuring compliance with regulatory requirements and company standards.

§ Participate in internal audits to maintain the highest standards of data integrity.

§ Work closely with cross-functional teams, including Clinical Development, Regulatory Affairs, and Medical Affairs, to ensure comprehensive safety monitoring.

§ Maintain accurate and up-to-date documentation of pharmacovigilance activities.

The above list reflects the general details necessary to describe the expectations of the position and shall not be construed as the only expectations that may be assigned for the position.

An individual in this position must be able to successfully perform the expectations listed above.

 

MINIMUM KNOWLEDGE, SKILLS AND ABILITIES:

§ Strong interest in pharmacovigilance, drug safety, and regulatory affairs.

§ Excellent organizational and communication skills.

§ Detail-oriented with the ability to work independently and collaboratively.

§ Proficiency in Microsoft Office applications.

 

DURATION AND COMPENSATION:

§ This internship is a 3-month position, with the possibility of extension based on performance. Compensation will be competitive and commensurate with qualifications and experience.

 

EDUCATION:

§ Currently enrolled in a relevant undergraduate or graduate program (Pharmacy, Life Sciences, Pharmacology, etc.).