TransPerfect Is More Than Just a Job Our greatest asset is our people, and nothing is more important to us than ensuring that everyone knows that. Each of our 90+ offices has its own individual identity, and each also has its own unique rewards.
TransPerfect is recruiting a Trial Master File Specialist II to work on a Contract Document Review Project. Details and requirements are below:
Start date: ASAP
Duration: 8 months
Location: South Plainfield, New Jersey. You will be on client site.
Hourly Rate: $50 per hour
Hours: 40 hours per week
Experience: 3 years working with regulatory documents in a pharma, biotech, CRO or related environment, including:
Thorough knowledge of essential regulatory documents required for the conduct of clinical studies, as described in the ICH E6 Guidelines and in relevant regulations (e.g., Food and Drug Administration (FDA) 21 CFR).
Knowledge and working experience with TMF Reference Model.
Proficiency with Microsoft Office.
Excellent verbal and written communication and skills.
Ability to work independently and collaboratively, as required, in a fast-paced, matrixed, team environment consisting of internal and external team members.
Analytical thinker with excellent problem-solving skills and the ability to adapt to changing priorities and deadlines.
Excellent planning, organization and time management skills including the ability to support and prioritize multiple projects.
Preferred qualifications include:
Associates and/or Bachelors degree.
Experience using eDMS software.
Demonstrated experience identifying, developing, and implementing improvements to departmental processes that increase efficiency and that maintain or improve quality (e.g., increasing the numbers of documents processed).
TransPerfect provides equal employment opportunity to all individuals regardless of their race, color, creed, religion, gender, age, sexual orientation, national origin, disability, veteran status, or any other characteristic protected by state, federal, or local law.