What are the responsibilities and job description for the Training and Placement Program – Clinical Data Management (CDM), Pharmacovigilance (PV) and Regulatory Affairs (RA) position at VForce Infotech?
VForce Infotech is a rapidly growing, minority-owned organization based in the United States, specializing in delivering top-tier human capital and professional services to mid-size and large organizations. With a focus on understanding client needs, the company excels in identifying and providing highly skilled professionals who exceed client expectations. Offering a wide range of IT services, VForce Infotech is a trusted partner for clients across various industries, delivering solutions in areas such as E-Business, Enterprise Application Integration, and Application Development. The company is committed to maintaining the highest standards through a highly competent team equipped with the knowledge and resources to provide exceptional services.
This is a full-time, on-site role for the Training and Placement Program focused on Clinical Data Management (CDM), Pharmacovigilance (PV), and Regulatory Affairs (RA). Based in Edison, NJ, participants in this program will gain hands-on training and development in essential areas such as clinical research data management, safety surveillance, and regulatory compliance. Day-to-day responsibilities include participating in instructional sessions, engaging in practical projects, and receiving tailored guidance to prepare for roles in these highly specialized fields. Program participants will also interact with industry professionals and gain insights into operational and regulatory practices.
- Effective Communication skills with the ability to convey ideas clearly and collaborate within a team environment
- Proficiency in Training and Development with expertise in conducting educational sessions and supporting professional growth
- Strong skills in Instructional Design with the capability to implement engaging and structured learning experiences
- Demonstrated Customer Service skills with a focus on understanding and meeting stakeholder needs
- Familiarity with Clinical Data Management (CDM), Pharmacovigilance (PV), or Regulatory Affairs (RA) is a plus
- Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or a related field is preferred
- Ability to learn and adapt quickly in a professional environment