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LAB TECHNOLOGIST - MICROBIOLOGY LAB Per Diem HOLY NAME MEDICAL CENTER TEANECK NJ Every Other Weekend Sat Sun 7 pm - 11 pm Fridays 4 pm - 8 30 pm..
Job Description Summary Job Description The Senior Manager Global Clinical Development GCD Project Management Office PMO reports to the Senior Director Worldwide Clinical Operations and is responsible for the day-to-day..
We are seeking a highly motivated per diem Clinical Assistant II for our growing organization Responsibilities include but are not limited to Tracks and maintains an inventory of supplies in..
The safety scientist has the overall responsibility for the safety of Luye's compounds. He/she will be working collaboratively within the Global Clinical Development organization. The responsibility includes: Being the Safety..
Title: QC Serologist I nLocation: Raritan, NJ nSchedule: 8am to 5pm Mon – Fri. nStart date: ASAP nResponsibilities: n n The QC Serologist I will be responsible for performing in-process..
We are seeking a highly motivated per diem Clinical Assistant II for our growing organization! Responsibilities include, but are not limited to: • Tracks and maintains an inventory of supplies..
Position Summary Taiho Oncology, Inc. works urgently to discover and develop innovative cancer treatments. As cancer evolves, we evolve with it?bringing novel technology to cornerstone chemotherapies, while at the same..
Job Description: Microscopically examine preparations for cytologic evaluation, correlating clinical information with morphologic findings to make a final diagnosis on negative gynecologic slides and render a microscopic assessment on abnormal..
Presented is a superb opportunity for an experienced Data Manager, with experience in medical device trials, to head up, lead and develop the data management group of a pioneering medical..
Summary: Coordinates and participates in clinical research studies conducted by principal investigators. Acts as a liaison for clinical investigators and IRB coordinators to ensure compliance of general and study specific..
Education Bachelor's Degree Skills XML Clinical Trials Analysis Skills SAS Troubleshooting Benefits Dental Insurance Health Insurance Paid Time Off Parental Leave Vision Insurance Join us in playing an important part..
The major responsibility of this position is to serve as a Medical Technologist in the Clinical Chemistry, Hematology, and Generalist sections of the laboratory. Duties/Responsibilities: Manual data entry of client..
Responsibilities: The QC Serologist I will be responsible for performing in-process and release testing of all types of BioVue cassettes and Gel Cards. This person will assure compliance with company..
Education Bachelor's Degree Skills Computer Literacy 401(k) Laboratory Experience Typing Communication Skills Benefits Health Insurance Paid Time Off 401(k) Matching Vision Insurance Disability Insurance Eurofins CRL Cosmetics, Inc. is searching..
Overview Position ID#10923 Responsibilities Assesses, diagnoses, intervenes with and plans for social work services related to patient and family bio-psycho-social needs and behaviors. Integrates assessment using information related to cultural,..
Education Doctoral Degree Master's Degree Skills Clinical Trials SAS Communication Skills R Benefits Dental Insurance Health Insurance Paid Time Off Parental Leave Vision Insurance Join us in playing an important..
Skills Computer Skills Clinical Research The Pain Management Center , a partner with Prospira PainCare, a national, single-specialty interventional pain practice with over 70 licensed providers in 30 locations across..
Clinical Research Associate - Drug Accountability Covance • Newark NJ 07102 Job #1076643036 Job Overview: Covance is seeking a CRA to cover the Northeast region of the US. This is..
New Brunswick, NJ is need of a traveling cytotechnologist.- Days - 9 weeks- Must meet CLIA Cytotechnologist requirements Please contact David at Aureus for more information or questions. email@example.com ;..
nnJob DescriptionnUnder the direction of TOM Development Unit Head, the Senior TOM will be accountable for the oversight and coordination of the global Monitoring operational aspects of assigned clinical trials..
An exciting new opportunity has just come available for a Clinical Documentation Specialist with a well-known academic medical center in New York.The Clinical Documentation Specialist will join a 400 bed..
nnJob Descriptionn Title : Documentation Specialist - II (Associate) n Duration: 1/6/2020 to 12/18/2020 n Location: Madison, New Jersey nnQualifications:nnBachelor’s degree (or equivalent work experience) with 7 years’ experience in..
Job Id: 4216nPosition Title: Clinical Trial Associate & Senior Clinical Trial AssociatenExternal Description:nnDo you know clinical trial regulatory documents like the back of your hands? Are you able to quickly..
Job Description: This is an exciting time to join our dynamic organization. OPKO Health is a diversified healthcare company that seeks to establish industry-leading positions in large, rapidly growing markets,..
Alphanumeric is hiring a Clinical Research Scientist to work in Warren, NJ with one of the largest pharmaceutical companies in the world. The purpose of this job is to support..
Education Bachelor's Degree Master's Degree Skills GCP Clinical Trials The Manager, CRU Operations and/or Clinical Research oversees the operational aspects of CRU projects to ensure all clients’ goals of quality,..