Recent Searches

You haven't searched anything yet.

2 Labels Design Associate - Clinical Trials Jobs in Malvern, PA

SET JOB ALERT
Details...
Clinigen
Malvern, PA | Full Time
$46k-59k (estimate)
1 Month Ago
Clinigen
Malvern, PA | Full Time
$46k-59k (estimate)
2 Weeks Ago
Labels Design Associate - Clinical Trials
Clinigen Malvern, PA
$46k-59k (estimate)
Full Time | Pharmaceutical 1 Month Ago
Save

sadSorry! This job is no longer available. Please explore similar jobs listed on the left.

Clinigen is Hiring a Labels Design Associate - Clinical Trials Near Malvern, PA

Clinigen is a rapidly growing global specialty pharmaceutical and services company with a unique combination of businesses. Our divisions operate in a complex global regulatory environment and ensure that vital medicines are delivered securely on time and wherever they are needed in the world.
The purpose of this position is to production of specialized labels for use on client specific projects for clinical trials and to provide support in the Operations Department with a variety of professional assignments.
Your role at Clinigen:
  • Produces clinical trial labels from approved label text proofs using the tabletop thermal transfer printer and associated software
  • Accurate and timely completion and filing of required paperwork
  • Maintain and receive clinical label inventory within Clinigen CSM's inventory management system
  • Actively update At Task following the completion of each labeling activity
  • Generates print randomizations from client kit lists
  • Responsible for communicating operational and personal concerns as well as opportunities for improvement to the department leadership
  • Perform routine cGMP inspections, disposition and maintenance of clinical trial materials
RequirementsTo be successful in this role you should have:
  • 1 year of related work experience in an office setting
  • 1 year of direct label experience
  • Familiar with the tools, concepts, and methodologies of label design (graphics) and printing desired
  • Experience with Standard Operating Procedures (SOPs), current Good Manufacturing Practices (cGMP), or Good Documentation Practices (GDP)
We're excited about you if you have:
  • Ability to work independently or within a team
  • Detail oriented to produce timely and accurate work
  • Excellent oral, written, and interpersonal communication skills with active listening ability
  • Self-motivated with exceptional time management skills to prioritize work and efficiently react to change in a fast paced environment
  • Maintain a high regard for confidentiality while dealing with all clients, proprietary, and pharmaceutical related information
  • Highly computer literate; experience operating with all Microsoft Office software
BenefitsWhile at Clinigen, you'll enjoy:The culture. Thanks to our diverse opportunities for engagement and involvement, every colleague's Clinigen experience can be a bit different, and we're proud of that. We work hard to ensure our company culture is inclusive to people from all backgrounds and social styles.
The transparency with leadership. All colleagues can share anonymous feedback with leadership on a weekly basis through our employee engagement platform. We use this feedback to inform our actions and decisions. We've been able to take steps to continuously improve how we do things at Clinigen.
The benefits. We take pride in having a broad range of activities, systems, and programs that provide a competitive benefit offering and build a culture of celebrating success.

Job Summary

JOB TYPE

Full Time

INDUSTRY

Pharmaceutical

SALARY

$46k-59k (estimate)

POST DATE

05/02/2024

EXPIRATION DATE

06/04/2024

WEBSITE

clinigengroup.com

HEADQUARTERS

BURTON-ON-TRENT

SIZE

200 - 500

FOUNDED

2010

CEO

PETER VANCE ALLEN

REVENUE

$500M - $1B

INDUSTRY

Pharmaceutical

Show more

Clinigen
Full Time
$52k-69k (estimate)
2 Days Ago
Clinigen
Full Time
$74k-95k (estimate)
2 Days Ago
Clinigen
Full Time
$67k-86k (estimate)
3 Days Ago