Clinical Research Administrative Assistant

Reposted Yesterday
Be an Early Applicant
Secaucus, NJ, USA
In-Office
20-22 Hourly
Entry level
Healthtech • Biotech • Pharmaceutical
The Role
The Clinical Research Administrative Assistant provides critical support, manages inquiries, coordinates meetings, schedules travel, and maintains expense records.
Summary Generated by Built In

                                                                                                            Clinical Research Administrative assistant 

Title: Clinical Research Administrative assistant

Location: Secaucus, NJ 

Part Time

Reports To: Senior Vice President

Frontage

 Frontage Laboratories Inc. is an award winning, publicly listed, full-service CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada, and China, growing significant YoY growth. Our core competencies include pre-clinical, drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.

 Position Summary:

We are seeking a proactive and detail-oriented Clinical Research Assistant to provide critical administrative and operational support within our research environment.

 Responsibilities:

  • Welcome and direct visitors and clients in a professional manner.
  • Respond to and resolve administrative inquiries and questions promptly.
  • Retrieves information as requested from study records, email, minutes, and other related documents; prepares written

summaries of data when needed

  • Responds to and resolves administrative inquiries and questions.
  • Coordinate and schedule complex travel, meetings, and appointments for the President and SVP.
  • Prepare detailed agendas and schedules for meetings to ensure productivity.
  • Retrieve information from study records, emails, meeting minutes, and other related documents as requested.
  • Prepare written data summaries and reports as needed.
  • Provide monthly expense and vendor invoices summaries.
  • Maintain a precise system for recording expenses using NetSuite.
  • Collaborate with Project Managers and Accounting to ensure all expense records are up-to-date and accurate.


Education and Requirements:

  • Strong computer skills including proficiency in use of Microsoft word, Excel, and PowerPoint 
  • Proven ability to successfully work in a team environment. Excellent oral and written communication skills
  • High school diploma/Certificate or educational equivalent; or equivalent combination of education training, and experience.


Salary: $20.00-$22.00/hour


Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.



Skills Required

  • High school diploma/Certificate or educational equivalent
  • Strong computer skills including proficiency in use of Microsoft Word, Excel, and PowerPoint
  • Excellent oral and written communication skills
  • Proven ability to successfully work in a team environment
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The Company
HQ: Exton, PA
591 Employees
Year Founded: 2001

What We Do

Frontage Laboratories, Inc. is a CRO that provides integrated, science-driven, product development services throughout the drug discovery and development process to enable pharmaceutical and biotechnology companies to achieve their development goals. Comprehensive services include drug metabolism and pharmacokinetics, analytical testing and formulation development, preclinical and clinical trial material manufacturing, bioanalysis, preclinical safety and toxicology assessment and early phase clinical studies. Frontage has enabled many biotechnology companies and leading pharmaceutical companies of varying sizes to advance a myriad of molecules through development and file regulatory submissions in the United States, China and other countries.

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