Clinical Medical Services Specialist III at Katalyst Healthcares Life Sciences
Madison, NJ 07940, USA -
Full Time


Start Date

Immediate

Expiry Date

19 Nov, 25

Salary

0.0

Posted On

20 Aug, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Process Management, Project Work, Communication Skills, Professional Manner, Internal Customers, Technology, Customer Service, Written Communication

Industry

Pharmaceuticals

Description

Job Description:

  • Conducting oversight of vendors who identify and collect adverse event and product quality complaint information and complete in-take of Pharmacovigilance safety and product complaint reports in Client’s Systems.
  • Conducting oversight of vendors to ensure collection, assessment, and processing of adverse event and product complaint information is performed in a compliant and timely manner to comply with global regulations.
  • Supporting the business strategy of assisting internal and external customers in collecting information for product safety reports, products complaints related to Client products.
  • Conducting oversight of vendors to ensure company standards for quality, compliance and productivity are met.
  • Remaining current on knowledge and skills required for supporting Client customers.
  • Supporting vendor case quality, and productivity metrics by exhibiting the Client core leadership attributes: Agile and Accountable; Clear and Courageous; Make Possibilities Real; All for One Client; Decide Smart and Sure.
  • Supporting and participating in audits and inspections as needed.
  • Supporting development of materials and delivering training in conjunction with the vendor, including train-the-trainer, special-topics, refresher, and internal Client trainings as needed.
  • Conducting oversight to ensure the vendor is effectively communicating using various mediums and establishing rapport with customers, colleagues, and interdepartmental groups.
  • Conducting oversight in the vendors use of multiple databases to document adverse event and product complaint information.
  • Supporting implementation of strategies to enhance PDI excellence in providing the highest level of customer experience.
  • Acts as an adverse event and product complaint intake subject matter expert.
  • Other duties may be assigned based on the need or work requirement of the organization.

Requirements:

  • Bachelor’s degree of RN, BSN, or BS Pharm/PharmD required.
  • 2-4 years’ clinical healthcare and previous pharmaceutical industry experience.
  • Pharmaceutical industry contact centre experience preferred.
  • Demonstrates ability to lead project work.
  • Proven success in results-driven process management.
  • Core knowledge of Industry regulations (ICH, FDA, EMEA, MHRA).
  • Demonstrates strong attention to detail and problem-solving skills.
  • Demonstrates strong verbal communication skills with external and internal customers.
  • Demonstrates strong (speed and accuracy) documentation skills.
  • Provides medical support with emphasis on the intake of medical product experiences.
  • Acts as a liaison with Quality Assurance for product quality problems where an adverse event is involved.
  • Works with Customer Service to provide standard information and product replacement as necessary.

Top skills:

  • Strong attention to detail when reviewing cases and doing quality assessments.
  • Excellence in verbal and written communication with peers, patients, and HCPs.
  • Ability to provide feedback in a professional manner.
  • Strategize in efficiency and technology improvements.
  • Ability to work in a constantly evolving environment.
Responsibilities

Please refer the Job description for details

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