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Biostatistics Network - NJ/PA
Hi James:
Happy Holidays! Spread the gift of opportunity to someone who may
need employment, a shorter commute, or a new challenge in the New
Year. Listed below are a few of the many projects we are currently
representing with our pharmaceutical and biotech clients. Could you help
us network our way to a few good people? If you can think of anyone
who may have interest (or is in a position to send this to more people),
please forward this email.
We appreciate your help.
Best wishes for a prosperous New Year,
Carolyn
Benslimane
Kim
Zinner
Stephanie Oscar
800-295-0332 x:
10
888-261-5162
800-525-3396 x: 258
I: Biostatistics Consultant (Oncology), Northern NJ - 5019
Company: Pharmaceutical
Company
Location:
Northern NJ
Status:
Full-time consulting engagement, 40 hrs/week
Length:
Long-term assignment in 12 month increments
Our client is one of the world's leading pharmaceutical company, both in
the US and Europe. Backed by a world-class R&D organization, they are
developing leading positions in seven major therapeutic areas:
cardiovascular disease, thrombosis, oncology, diabetes, central nervous
system, internal medicine, and vaccines.
Provides statistical analyses, summaries and reports of studies in the
support of product development including New Drug applications (NDAs) and
Biological License Applications (BLAs) submissions. Ensuring statistical
and integrated clinical/statistical reports meet regulatory and company
standards. Presents and interprets data manipulations/processing and
statistical analyses. Derives statistical conclusions and makes
recommendations based on experimental results.
Requirements: At least MS degree in Biostatistics or related field,
PhD is preferable. Candidate should have biostatistics experience
with and a broad understanding of clinical trials in oncology.
Statistical analyses, tabulations, graphics and listings of clinical
trial data. Offer guidance in statistical analysis methodology. Ability
to coordinate the production of data displays in an efficient manner for
inclusion in integrated clinical/statistical reports and other similar
reports. Broad knowledge of SAS. Proven ability to organize
workload and priorities and complete tasks on time. Demonstrated ability
to work effectively in a team environment. Strong interpersonal skills
and ability to communicate effectively. Ability to complete tasks under
limited supervision.
II: Biostatistics Consultant (CNS), Philadelphia Metro - 4866
Company: Pharmaceutical
Company
Status:
Full-time consulting engagement, 40 hrs/week
Length:
Long term assignment in 12 month increments
In this large, multi-national company, all employees and contractors are
considered as individuals, with respect paid to recognize their
merit. This client is known for keeping contractors equally
involved in project decisions; with opinions and individual contributions
valued on the same level as that of internal staff.
We are seeking a consultant statistician to support phase II studies in
the CNS and Internal Medicine area. Specific work will include
developing statistical analysis plans and programming specifications,
working with programmers to implement the planned analyses, validating
SAS output, supporting Data Monitoring Committee activities, performing
ad hoc analyses to facilitate decision-making. Working with
clinicians and medical writers to complete study reports.
Requirements: Masters or PhD in statistics. 3 to 5 years experience
in the pharmaceutical industry; SAS and other computer language
programming skills are required. Clinical trial experience in CNS
and Internal Medicine are also desirable.
III: Biostatistics Consultant (Internal Med), Northern NJ - 5147
Company: Pharmaceutical
Company
Status:
Full-time consulting engagement, 40 hrs/week
Length:
Long-term assignment in 6 month increments
In this large, multi-national company, all employees and contractors are
considered as individuals, with respect paid to recognize their
merit. This client is known for keeping contractors equally
involved in project decisions; with opinions and individual contributions
valued on the same level as that of internal staff.
In this role the statistician will support the internal medicine TA in
Phase II - III trials. The consultant will develop SAP, perform
data verification, and work with programmers on program
specifications. Will conduct statistical analysis to address ad hoc
requests.
Requirements: MS or PhD in statistics (PhD preferred),
biostatistics or related experience. At least 4-6 years experience
in clinical trials, with pharmaceutical industry experience
preferred. Strong hands-on SAS programming skills.
Ability to work independently. Good communication
skills---both verbal and written. Experience with writing SAPs and
reports. Able to work on-site in Northern NJ.
IV: Biostatistics Consultant, Northern NJ - 5155
Company: Pharmaceutical
Company
Status:
Full-time consulting engagement, 40 hrs/week
Length:
Long-term assignment in 6 month increments
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.
Participate in study design, review protocols and estimate sample sizes
for headquarter sponsored studies. Determine appropriate
statistical procedures and write statistics sections of protocol.
Manage and/or conduct study related statistical activities including the
cross-functional interactions. Stay abreast of developments in
clinical and statistical research. Participate in project
meetings and present the risk assessment from the statistical/product
point of view. Review study materials (e.g., CRF, CSR) to ensure
conformity with protocol content. Prepare, QC, document, maintain
and archive statistical procedures and programs. Has good
programming skill in performing statistical analyses, generating efficacy
tables and figures. Participate in the activities related to
publications. Assist functions related to the product Strategic
Review Team (SRT) and country operated study activities.
Requirements: PhD with 2-3 years of experience in the
pharmaceutical Industry. Experience in generating tables and graphs
using the SAS software. Good communication and interpersonal
skills. Phase IV experience is a plus.
========================
To search all contract & perm openings nationwide, go to:
http://cambridgegroup.com/pharmaceutical/search.shtml
To refer someone for a fee, go to:
http://cambridgegroup.com/pharmaceutical_contracting/refer.shtml
========================
The Cambridge Group, Ltd.
Founded in 1976, The Cambridge Group has developed a reputation as one
of
the most respected recruiting firms specializing in clinical trials.
Our
well-established client network, continually developed over almost
30
years, retain us not only to represent candidates with the right skill
sets;
but to go beyond and represent only those professionals who excel and
are
considered to stand out amongst their peers.
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, TN-1 visa, H-1 visa, and sponsorship
for permanent residency (green card) immediately upon hire as
appropriate.
www.cambridgegroup.com/pharmaceutical_contracting
The Cambridge Group Ltd.,
Your Success Is Our Business
*** You are receiving this message as a recognized member of the
pharmaceutical community, and as such we are seeking candidate referrals
on
behalf of our clients for the position detailed above. If you know of
any
colleagues or friends who possess this background, please forward
this
message to them for reference. We offer up to a $2,500 fee for each
candidate who is placed by referral. Full details on referral policy can
be found at
http://www.cambridgegroup.com/pharmaceutical_contracting/refer.shtml
If
you would like to be removed from future mailings, please reply with the
word REMOVE in the subject line***
The Cambridge Group, Ltd 1175 Post Road East Westport,
CT 06880
800-525-3396 800-295-0332
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