Monday, March 16, 2009

Medical Writing Jobs

These openings are advertised through the Medical Wrting Yahoo group:

From: Stephanie Oscar
The Cambridge Group Ltd.
800-525-3396 ext. 258

contract@cambridgeg roup.com

I: Medical Writer - 6071
Company: Pharmaceutical Company
Location: Northern NJ, primarily on-site
Status: Long-term consulting engagement
Length: Long-term assignment: initial term 6 months

This NJ-based global pharmaceutical company believes that having the
right people in the right jobs is critical to advancing their action
agenda and becoming a high-performance competitor for the long term. The
company seeks to identify and attract people with superior talent, skills
and winning attitudes. They are creating an environment of continuous
learning and strive to engage colleagues through a unique and inclusive
culture where people are energized, excited and committed to
shared goals and values.

Seeking a contract medical writer to write and QC regulatory submissions,
clinical study reports, investigator brochures and integrated summaries.
Work must be performed primarily on-site.

Requirements: At least 2 years experience in clinical writing for
regulatory submissions including clinical study reports, investigator
brochures and integrated summaries. Advanced degree in Life Sciences,
preferably PhD or PharmD

II: Medical Writer - 6255
Company: Pharmaceutical Company
Location: Northern NJ - on-site
Status: Full-time Consulting Engagement, 40 hours/week
Length: Long-term assignment in 6 month increments

Our client is a company that wants to be recognized for having a positive
impact on people's lives with their products by meeting needs and
surpassing expectations. The company strives to build a reputation for an
exciting workplace in which all employees and contractors can realize
their professional ambitions.

The main objective of this role is project management of clinical report
completion. Responsibilities include: Tracking of reporting status for
Translation Medicine group (Early development- Phase 1 and 2a). Tracking
of key deliverables by cross functional team members. Integration of
clinical information (protocol, amendments, monitoring trip reports and
clinical data) to produce a high quality clinical study report.
Functional liaison between clinical trial team and DOC publishing and/or
DRA operations group. Scope of documents may include IB updates, IND
updates and other key documents as required.

Requirements: Minimum life science degree or equivalent. Higher degree
desirable. Excellent written and oral command of English language. At
least 6 years medical writing experience or other relevant pharma
industry experience combined with scientific and regulatory knowledge,
plus knowledge of the medical writing processes. Expert data
interpretation and presentation skills. Extensive experience with
clinical documentation, formats and publication writing.

* *

The Cambridge Group, Ltd. offers a cafeteria-style, flexible benefits
plan where consultants can choose from:

-Two different Blue Cross Health Plans
-Dental Insurance
-401k
-Life Insurance & AD&D
-Long-term Disability
-Paid Holidays
-Up to 4 weeks of Vacation
-Continuing Education Reimbursement up to $5,250 /yr
-Section 529 Tax-Deferred College Savings Plan

We also offer relocation benefits, H-1 visa, and sponsorship for
permanent residency (green card) immediately upon hire as appropriate.

2 comments:

Danish said...
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