Prestige Biopharma Pte Ltd – Project Intern (Clinical Trial)

Company
Prestige Biopharma Pte Ltd
pbpsg.com
Designation
Project Intern (Clinical Trial)
Date Listed
09 Jul 2019
Job Type
Entry Level / Junior Executive
Intern/TS
Job Period
Immediate Start, For At Least 5 Months
Profession
Marketing / Public Relations
Industry
Healthcare / Fitness / Sports
Location Name
2 Science Park Drive, Singapore
Address
2 Science Park Dr, Singapore 118222
Map
Allowance / Remuneration
$800 - 1,000 monthly
Company Profile

Prestige BioPharma (PBP) is a Singapore based biopharmaceutical company focusing on development of biosimilars and new antibody therapeutics. PBP has strong presence and networks in Asia Pacific region and actively penetrating into the global pharmaceutical market. The successful completion of phase I clinical trial on its first biosimilar HD201 (Trastuzumab) in EU, 2014, has placed PBP amongst the top-tier biosimilar developers.

Job Description

Internship Description:

Our company focuses on development of biosimilars and new antibody therapeutics, from the discovery phase till clinical phases down the development pipeline. We are currently looking for an intern to assist the routine work duties within the company.


Job Functions and Responsibilities:

·      Maintainenace of Prestige BioPharma’s Website and company materials

·      Research work corresponding to the biosimilars and antibody drugs listed in the pipelines

  •   Bioanalyatical Related
  •   Toxicological Related
  •   Efficacy Related
  •   Cell Biology Related

·      To expose and learn about Quality Assurance Related Work

  •   OECD compliance
  •   US FDA GLP compliance
  •   GMP Compliance on CMO production and QP Release

·      To have a broad landscape about Clinical Trial Management:

  •    Monitoring of trial status
  •    Logistics Management and Monitoring of Drugs
  •    IVRS System Overall and Monitoring
  •    Ongoing Study Monitoring  
  •    Budget and Timeline Management
  •    Daily Communications and Followup with Vendors and CROs
  •    Regulatory Affairs Related (EMA, Clinicaltrials.gov etc)
  •    Market Research Projects

·      Daily Ad-hoc General Adminstrative Duties:

  •    Assist in Presentation/Brochure Making for the company
  •    Assist with Guests‘ Visits
  •    Any other tasks assigned
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