Clinical Specialist – Post-Market Surveillance

MillenniumSoft Inc; Franklin Lakes (NJ); On-site; USD 80,000 - 110,000; Full time

Job summary

A leading medical device company seeks a Clinical Specialist for Post-Market Surveillance in Franklin Lakes, NJ. The role includes conducting customer surveys, maintaining relationships, and providing technical support. Applicants should have a background in clinical laboratory science and possess strong problem-solving and communication skills.

Qualifications

• 3–5 years of experience in clinical laboratory science preferred.
• Knowledge of medical device safety reporting is a plus.

Responsibilities

• Conduct customer surveys and report product issues.
• Establish and maintain relationships with customers and various teams.
• Document all customer inquiries in system records.

Skills

Communication

Problem Solving

Customer Service

Clinical Laboratory Knowledge

Technical Skills

Education

BS Degree in medical technology, biology, chemistry, or other health sciences

ASCP or equivalent certification

Job description

Clinical Specialist – Post-Market Surveillance

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Clinical Specialist – Post-Market Surveillance

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Position : Clinical Specialist – Post-Market Surveillance

Location : Franklin Lakes, NJ

Duration : 6 Months contract

Total Hours/week : 40.00

Client: Medical Device Company

Job Category: Sales Support

Level of Experience: Mid-Level

Employment Type: Contract on W2 (Need US Citizens or GC Holders Only)

Job Description

Job Summary:

• This position participates in Post Market Surveillance (PMS) activities with customers.
• The Clinical Specialist – Post-Market Surveillance associate will demonstrate technical skills in disciplines of clinical laboratory science such as specimen collection, clinical chemistry, hematology, coagulation, immunohematology, molecular diagnostics, urinalysis and urine culture, infectious disease and virology.
• Additionally, the associate will remain current in clinical laboratory science by participating in continuing education programs, and in department LEAN, Quality, and Continuous Improvement activities.
• As needed, the associate may offer technical counsel to Sales, Marketing, R&D, QA, and Regulatory Affairs.
  
  

Primary Duties, Responsibilities & Authorities

• Conducts customer surveys for client products following the client Vacutainer Tube Products Post Market Surveillance Quality Plan.
• Report product issues from customers to the client complaints team and supports the complaint handling process.
• Establish and as needed maintain relationships with customers, dealers, distributors, IDS sales reps, country managers, product managers, regional technical specialists, and other functional areas to perform position functions.
• Maintains detailed practical knowledge of specific products as they relate to new and existing instrumentation, new diagnostic tests, etc.
• Works on issues where analysis of situation or data requires review of relevant factors.
• Exercises judgment within defined procedures to determine if additional actions are needed by other functions in the organization.
• Documents all customer inquiries and related activities in the identified validated system of record for Technical Support according to established work instructions and job aids.
• Provides customer product leads to client Specimen Management associates for potential sales opportunities.
• Works in conjunction with the client Specimen Management associates to win, defend, and grow the client IDS business.
• Attends relevant meetings to obtain Quality and Regulatory updates.
• Participates in case studies sessions to develop and enhance troubleshooting and problem- solving skills.
• Attends at least one educational session per year to stay abreast of current technology and trends in clinical laboratory science.
  
  

Knowledge And Skills

• Ability to understand and translate customer issues and provides solutions.
• Good communications skills, both written and verbal.
• Ability to work cross-culturally.
• Proficiency with PCs and software such as word-processing and spreadsheet applications.
• Ability to make good use of minimal resources.
• Ability to coordinate multiple activities, visualize future steps.
• Able to communicate with technical and non-technical persons.
• Ability to utilize tact and diplomacy in dealing with people.
• Excellent customer service skills.
• Good background in problem solving.
• Knowledge of specimen collection and management techniques.
• Knowledge of the preanalytical phase of the total laboratory testing process.
• Knowledge of scientific methodologies and clinical laboratory medicine.
  
  

Education And Experience

• BS Degree in medical technology, biology, chemistry, or other health sciences.
• ASCP or equivalent certification preferred.
• 3–5 years of experience in various aspects of clinical laboratory science preferred. Practical knowledge and experience with medical device safety reporting is a plus.
• Knowledge of IDS-Specimen Management products, related competitor products, and clinical laboratory instrumentation are strongly desired.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Contract

Job function

• Job function

  Health Care Provider

• Industries

  Staffing and Recruiting

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