[The logo is protected from the company]

Covance Inc.

Covance, with headquarters in Princeton, New Jersey, is one of the world’s largest and most comprehensive drug development services companies, with annual revenues greater than $2 billion, employees in more than 60 countries, and more than 11,000 employees worldwide.    NONCLINICAL DEVELOPMENT(Toxicology, Research Products, Analytical Services)    * Managed 443 compound development programs (>250 IND/CTA enabling), with over 100 different sponsors, which led to 41 IND/CTA applications in 2... Read More

Address      210 Carnegie Ctr Princeton, NJ 08540 (609) 452-8550
Website      www.covance.com/
Holding      No Holding Details

View Company Page
Apply to job

Senior Clinical Project Admin

    We are currently seeking multiple Sr. Clinical Project administrators for our Princeton, NJ office.

Job Duties:
•Train and mentor Clinical Project Administrators
•Provide clerical support to project team (e.g., word processing, proofreading and editing correspondence, large and small documents, mailings, shipment of study files, fax and photocopy documents, assemble study documents, and arrange meetings, etc.)
•Set up and maintain clinical investigator files and documentation
•Prepare study-related documents and other materials for delivery to archives, at appropriate intervals
•Prepare investigator budget payments and tracking systems; generate tracking reports as assigned
•Prepare monitoring visit documentation for Clinical Research Assistants and above, as requested by supervisor
•Data entry and maintenance of selected study tracking data
•Assist with coordinating vendors
•Organize/prepare for client meetings/teleconferences
•Assist/prepare for client or internal audits
•Provide telephone coverage and related support duties
•Perform other administrative duties as assigned by management
Education/Qualifications    Required:
•Diploma – Secondary Education or equivalent

Preferred:
•Thorough knowledge of the contents of investigator documents and the applicable regulations and Covance Standard Operating Procedures for their use
Experience    Required:
•Minimum of four (4) years administrative experience in a corporate environment or, minimum of four (4) years Clinical Project Administrator experience
•Demonstrated aptitude for training
•Good oral and written communication skills
•Ability to set priorities and handle multiple tasks simultaneously
•Good organizational and time management skills
•Computer literacy (word processing and spreadsheet software)
•Good typing skills
•Good spelling and proofreading skills
•Aptitude for handling and reviewing numerical data
•Ability to operate standard office equipment (e.g., fax, copier)
•Works efficiently and effectively in a matrix environment
•Fluent in local office language and in English, both written and verbal
EEO Employer    Covance is committed to diversity in the workplace and is an equal opportunity employer. (M/F/D/V). Your confidentiality and privacy are important to us.

Other Job Information

Vacancy type:

Full Time

Contact Mode:

not provided

Fax:

+1-302-6555049

Contact Name:

not provided

Job Duration:

not provided

Phone:

+1-609-4524440

Email:

not provided

News - Covance Inc.

Related Jobs

Clinical Research Associate

Primary responsibility is ensuring that clinical studies ...   [more]

Pre-Clinical Technician III

Performs the daily care of the research vivarium, which ...   [more]

Clinical Research Associate

Designs, plans, and implements clinical research project ...   [more]

Clinical Research

Manages operational strategies for designated programs.  ...   [more]

Clinical Research Associate

Cepheid administers its personnel policies and conducts ...   [more]

Senior Study Manager Job

Celgene Corporation is committed to delivering innovativ ...   [more]

Clinical Research Physician

Celgene Corporation is committed to delivering innovativ ...   [more]

Clinical Research Physician Job

Celgene Corporation is committed to delivering innovativ ...   [more]

Expand

Collapse