Scientist - II (Associate)

Immediate need for a talented Scientist - II (Associate). This is a 12+ months Contract opportunity with long-term potential and is located in Rahway, NJ(Onsite). Please review the job description below and contact me ASAP if you are interested.Job ID: 24-21378Pay Range: $30 - $35/hour. Employee benefits include, but are not limited to, health insurance...

Immediate need for a talented Scientist - II (Associate). This is a 12+ months Contract opportunity with long-term potential and is located in Rahway, NJ(Onsite). Please review the job description below and contact me ASAP if you are interested.Job ID: 24-21378Pay Range: $30 - $35/hour. Employee benefits include, but are not limited to, health insurance...

Job Description: Analytical R&D group at Merck is looking for a qualified scientist. Conducts release and stability testing of drug products following SOPs and cGMPs. Plans and executes validation of analytical methods. May develop and/or adapt methods. Solves more complex problems with some guidance from senior scientists. Troubleshoots...

Job Description: Analytical R&D group at Merck is looking for a qualified scientist. • Conducts release and stability testing of drug products following SOPs and cGMPs. • Plans and executes validation of analytical methods. • May develop and/or adapt methods. • Solves more complex problems with some guidance from senior scientists. • Troubleshoots...

Job DescriptionJob DescriptionSummary:Under the general direction of the Patient-Centered Endpoints & Strategy (PaCES) group lead, the Associate Principal Scientist has responsibility for coordinating global Clinical Outcomes Assessment (COA) endpoint strategies, including Patient-Reported Outcomes (PROs) for specific disease areas.The individual will...

Responsibilities:Under the general direction of the Patient-Centered Endpoints & Strategy (PaCES) group lead, the Associate Principal Scientist has responsibility for coordinating global Clinical Outcomes Assessment (COA) endpoint strategies, including Patient-Reported Outcomes (PROs) for specific disease areas.The individual will support teams on the...

Responsibilities:Under the general direction of the Patient-Centered Endpoints & Strategy (PaCES) group lead, the Associate Principal Scientist has responsibility for coordinating global Clinical Outcomes Assessment (COA) endpoint strategies, including Patient-Reported Outcomes (PROs) for specific disease areas.The individual will support teams on the...

Responsibilities:Under the general direction of the Patient-Centered Endpoints & Strategy (PaCES) group lead, the Associate Principal Scientist has responsibility for coordinating global Clinical Outcomes Assessment (COA) endpoint strategies, including Patient-Reported Outcomes (PROs) for specific disease areas.The individual will support teams on the...

Immediate need for a talented Associate Principal Scientist. This is a 24+ Months Contract opportunity with long-term potential and is located in West Point, PA / Rahway, NJ(Onsite). Please review the job description below and contact me ASAP if you are interested.Job ID:24-23938Pay Range: $61 - $71/hour. Employee benefits include, but are not limited to,...

Regulatory Operations Specialists - II (Associate) Rahway, NJ- Hybrid schedule (require to be onsite for 3 days/week -Tuesday and Wednesday fixed) 3rd day is optional. 12 Months contract Pay Rate: $26.56/hr on w2•Under general supervision, responsible for the preparation of high-quality labeling documents for submission to the US Food and Drug...

On-Board Scientific is hiring an Associate Principal Scientist (Clinical Outcomes Assessment) based out of West Point, PA or Rahway, NJ! Hybrid For immediate consideration please send your resume to Subject Line: Position Title and State you are located.   About Us: On-Board Services, Incorporated is an on-site contract service provider for a local...

The Fountain Group. We are a national staffing firm and are currently seeking a Scientist (Clinical Outcome Assessment) for a prominent Pharmaceutical client of ours. This is a hybrid role and can sit in either Rahway, NJ or West Point, PA. Details for the position are as follows:   Job Description: Pay: 48.00-58.00/hr. 2 year contract assignment to...

Regulatory Operations Specialists - II (Associate) Job ID: 24-02608 Qualifications: Title: Labeling Specialist Education: Associate/Bachelor of Life Science/Master's degree. Required Experience and Skills: * With Associate, minimum 5 years of relevant experience within pharmaceutical labeling experience * With Bachelor's, minimum 3 years of relevant...

Regulatory Operations Specialists - II (Associate) Rahway, NJ- Hybrid schedule (require to be onsite for 3 days/week -Tuesday and Wednesday fixed) 3rd day is optional. 12 Months contract Pay Rate: $26.56/hr on w2 •Under general supervision, responsible for the preparation of high-quality labeling documents for submission to the US Food and Drug...

**Position Description**: **Associate Specialist - Operations Support** The Enabling Facilities (EF) group within the Chemical Engineering Research & Development (CERD) Department is seeking a highly motivated individual to work in a fast-paced job that provides a high degree of technical and project management responsibility. The Associate Specialist...

Regulatory Operations Specialists - II (Associate) Job ID: 23-03525 Qualifications: Education Requirements: • Bachelor's degree in a relevant discipline such as animal science, veterinary technology, immunology, toxicology/pharmacology, chemistry, biology, business, regulatory or law - OR- • Master's degree in a relevant discipline Required Experience...

•Under general supervision, responsible for the preparation of high-quality labeling documents for submission to the US Food and Drug Administration (FDA). •Ensure that product labeling is updated in accordance with FDA regulations and corporate guidelines. •Ensure prompt availability of labels and artworks and liaises with departments such as...

•Under general supervision, responsible for the preparation of high-quality labeling documents for submission to the US Food and Drug Administration (FDA). •Ensure that product labeling is updated in accordance with FDA regulations and corporate guidelines. •Ensure prompt availability of labels and artworks and liaises with departments such as...

" Under general supervision, responsible for the preparation of high-quality labeling documents for submission to the US Food and Drug Administration (FDA). " Ensure that product labeling is updated in accordance with FDA regulations and corporate guidelines. " Ensure prompt availability of labels and artworks and liaises with departments such as...

Job ID: 24-02608 Qualifications: Title: Labeling Specialist Education: Associate/Bachelor of Life Science/Master's degree. Required Experience and Skills: •With Associate, minimum 5 years of relevant experience within pharmaceutical labeling experience •With Bachelor's, minimum 3 years of relevant experience within pharmaceutical labeling experience...