Research and Development Scientist

Date Posted: 12/04/2024

Hiring Organization: Rose International

Position Number: 475191

Job Title: Research and Development Scientist

Job Location: Valhalla, NY, USA, 10595

Work Model: Onsite

Employment Type: Temporary

Estimated Duration (In months): 13

Min Hourly Rate ($): 35.00

Max Hourly Rate ($): 40.00

Must Have Skills/Attributes: Clinical, Communications, GCP, Nutrition, Research, Science

Required Education:

• M.S. required in Exercise Physiology/Kinesiology/Nutrition or related discipline

Required Qualifications/Skills/Experience:

• Two or more years of experience in clinical research (can include experience gained during M.S. thesis work)

• Demonstrable knowledge of and following of good clinical practice (GCP) guidelines

• Demonstrable knowledge of human physiology

• Two or more years of experience in clinical research (can include experience gained during M.S. thesis work)

• Must have a pro-active work style, able to multitask, and be flexible to work in a high-performance and ever-changing environment

• Self-starter with good interpersonal communication skills and ability to work with various personalities and work styles

Research and Development Scientist Overview:

Client is committed to helping athletes optimize their health and performance through research and education in hydration and nutrition science. Recently, Client has embarked on a new project to expand the research and athlete testing facility in Valhalla. This facility is responsible for conducting efficacy research on functional ingredients for hydration. As a part of Client, the incumbent of this Scientist role will be responsible for representing Client and the Client R&D teams with high standards and in accordance with ethical guidelines for human research and conduct.

Job Duties:

• Execute the laboratory-based clinical research studies at Client research hub in Valhalla, NY

• Assisting in the day-to-day execution of research projects including data collection, data entry, and writing of internal reports

• Ensure research program safety standards and development/execution of related SOPs

• Conducting medical screenings (blood pressure, fasting blood glucose) to determine participant eligibility for entry into Client clinical research trials

Hours:

• 7-5, Mon-Fri with flexibility and willingness to work during non-traditional hours (e.g., start time before 8:00am or finish time after 5:00pm) as needed depending upon research schedule

**Only those lawfully authorized to work in the designated country associated with the position will be considered. **

**Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements. **

Benefits:

For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website.

California Pay Equity:

For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here.