Human Resource Specialist |
| Diagnostica Stago, Inc. is the exclusive provider of Diagnostica Stago Hemostasis product lines in ... |
|
Manager, Internal Audit |
| MANAGER, INTERNAL AUDIT
Description:
The Manager, Internal Audit will be ... |
|
Hotline Agent |
| Diagnostica Stago, Inc. is the exclusive provider of Diagnostica Stago Hemostasis product lines in ... |
|
Assoc. Director, Drug Safety, Top North NJ Pharma |
| Assoc. Director, Drug Safety, Top North NJ Pharma
Summary: A top pharmaceutical company in ... |
|
Sr. Director / Director - PreIND & Phase I |
| Senior Director / Director – PreIND & Phase I Job Statement/Job Purpose:The position of D... |
|
Enterprise Market Specialist, Life Sciences Service & Support |
|
Enterprise Market Specialist, Life Sciences Service & Support
About the job&... |
|
Chief Operating Officer - India |
| Chief Operating Officer The Port City Group, Inc. is representing a well-diversified ... |
|
Senior Manager, Sales & Marketing Technology |
|
SENIOR MANAGER,
SALES & MARKETING TECHNOLOGY
Description:
This position ... |
|
Research Assistant |
| Entry level position in pharmaceutical research company.
College graduate. Above average ... |
|
General Administrative |
| Job Purpose:
Provides office services by supporting team members, and monitoring administrative ... |
|
|
Senior Level Medical Writer (Project Management)
| Details |
Country: USA
Location: New Jersey-Northern US-NJ-Northern
Total applied: 28 Job Category:Biotech/R&D/Science
Relevant Work Experience:2+ to 5 Years
Education Level:Bachelor's Degree
Location:US-NJ-Northern
Status:Full Time, Employee
Occupations:Clinical Research;Pharmaceutical Research
Career Level:Experienced (Non-Manager)
Relevant Work Experience:2+ to 5 Years
|
|
Senior Level Medical Writer (Project Management)
Our client is a mid-sized Pharmaceutical Company currently focusing in the areas of Diabetes and Oncology and conducting Global Clinical Trials on various compounds in these therapeutic areas. Our client is looking to add a Senior Level Medical Writer to its staff.
The Senior Medical Writer will be developing, revising and updating Protocols and Clinical Study Reports for Pre-clinical and Clinical Studies, Investigator’s Brochures, components of IND’s, CTA’s, NDA Submissions and other Clinical and Regulatory documents.
Project Management experience including demonstration of planning and excellent organizational skills with minimal supervision required. Additionally, this individual will be responsible for providing support to the Clinical Development Teams. Lastly, this person will mentoring Junior Staff Members and Consultants.
The ideal candidate for the Senior Medical Writer’s position will have:A minimum of a Bachelors Degree in one of the Life Sciences, Nursing or Medical Sciences; Masters Degree, PharmD or PhD a plus.At least three years of Medical Writing experienceExperience within the Pharmaceutical Industry, Phases I-IV drug developmentKnowledge of ECTD and ICH document regulations and familiarity with the AMA Manual of Style guidelines.MS Office skills
In return for your expertise, our client offers:Affordable Health, Dental and Vision Care choices for Employees and their families.Health and Dependent Care Reimbursement accounts.Domestic Partner BenefitsLife and Disability Income Protection plansDiscounts on various products and servicesAssistance services for personal issues, childcare referrals, financial/legal questionsRetirement Savings and Stock Purchase Plans, including 401k with Company matchEmployee recognition bonusesFlexible Working Arrangements in some casesCompany Paid Time OffFloating and Company holidaysEducation Assistance for continuing professional development
Interested/Qualified Candidates, please send your complete CV/Resume in MS Word format to Caryn Reiman, caryn@ultimatesolutions.com or call (201) 909-3717 for more information.
|
| Related jobs |
|
|
Pharmaceutical Market Research Manager
Celgene Corporation is committed to delivering innovative therapies designed to improve the lives of patients worldwide. We are a global biopharmaceutical company ...
|
|
|
Medical Writer - Regulatory Affairs and Clinical Trials
Our client is a rapidly growing small pharmaceutical company with many drugs in various stages of development for indications such as CNS, Immunology, Cardiovascular ...
|
|
|
Associate Director of Clinical Pharmacology or Senior Clinical Pharmacologist
Our client, a rapidly growing Global Pharmaceutical company with many drugs in various stages of development for Schizophrenia, Alzheimers Disease, Immunological Disease,...
|
|
|
Sales Administration Specialist
Diagnostica Stago, Inc. is the exclusive provider of Diagnostica Stago Hemostasis product lines in the United States. Diagnostica Stago, Inc. offers a complete ...
|
|
|
Computer Validation Engineer
Actavis is a strong leader in the development, manufacture and sales of first-class generic pharmaceuticals with operations in 32 countries, products registered in more ...
|
|
|
Molecular Cytogenetics Research Technician
Cancer Genetics, Inc. (CGI) is a rapidly expanding diagnostic, genomics research, and DNA diagnostics probe company, and a pioneer in developing disease specific CGH A...
|
|
|
Awesome Sr. Product Manager Position
Must have strong Marketing Experience
Key product manager role responsible for product management activities required to implement and administer Sub-unit and Platform ...
|
|
|
Materials Management Coordinator
General Description
Responsible for performing release testing on cellular products manufacturing in a cGMP clinical laboratory environment. Activities include ...
|
|
|
Quality Control Technician
Progenitor Cell Therapy, L.L.C. is a company offering cellular engineering services for Pre-clinical development, Clinical Trials and Cellular Manufacturing to B...
|
|
|
Manager, Treasury Operations and Controls
MANAGER, TREASURY OPERATIONS
AND CONTROLS
Description:
The Manager, Treasury Operations and Controls is accountable for the management of day-to-day T...
|
|
|