Job Description. Delivering rapid and professional communication. Developing trust and positive relationships with clients. Providing anticipatory guidance for questions or concerns. Make Scorpion product recommendations where suitable. Translate product enthusiasm and capability into assisting clients with new products and services. Motivated to engage with clients via video communication, phone, email or otherwise to educate, assist and provide...
Job Description. We are currently recruiting a. Bioanalytical Chemist. to join our team in. Richmond, VA. or we are open to. remote work arrangements. As a Bioanalytical Chemist, you will apply your chemistry knowledge and data analytics skills to provide scientific expertise to Clinical and Biological Activity groups in support of development of novel reduced-harm tobacco products and in compliance with regulatory requirements. What you will be ...
$20,000 SIGN ON BONUS AVAILABLE. Must have a minimum of 1-year of Cath Lab experience to qualify. Shift/Weekend Rotation. Monday – Friday. 8-hour shifts: 7am – 3:30pm. Call Schedule. 10-13 nights/month. minimum 1-2 weekend/month. Volume/Caseload. 30 plus scheduled cases per week. Types of Procedures. TCAR, AAA, Peripheral vascular, Pacemakers, Defibrillators, Right and Left Heart Cath, STEMI, and Stroke. PRIMARY (ESSENTIAL) DUTIES. . Demonstrates...
Position Summary / Objective. Supports the Worldwide Patient Safety Vision through understanding the impact and implication of daily work on all customers of AE Processing. This commitment drives dedication to quality and accurate case handling, for overall contribution to a high performance team. Position Responsibilities. Ensures the quality and accuracy of adverse event reports. Learns and navigates the intricacies of the BMS Drug Safety Datab...
We are currently hiring full-time office based individuals for an exciting career in clinical research managing our Trial Master File. The Trial Master File (TMF) is a collection of documentation that allows the conduct of a clinical trial, and the integrity of the data produced to be evaluated by Regulatory bodies, such as the FDA. The TMF is an important tool, and can help teams manage trials more effectively and ultimately plays a big role in ...
Responsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee, this position will serve as support for the clinical study team. Essential Duties And Responsibilities. Participate and assist in design and preparation of protocols and case report forms. Generate clinical SOPs, policies, charters, and plans according to US and international guidelines. Participate in the evaluation of pote...
Responsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee, this position will serve as support for the clinical study team. Essential Duties And Responsibilities. Participate and assist in design and preparation of protocols and case report forms. Generate clinical SOPs, policies, charters, and plans according to US and international guidelines. Participate in the evaluation of pote...
Job Description. Responsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee, this position will serve as support for the clinical study team. Essential Duties And Responsibilities. Participate and assist in design and preparation of protocols and case report forms. Generate clinical SOPs, policies, charters, and plans according to US and international guidelines. Participate in the e...
Responsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee, this position will serve as support for the clinical study team. Essential Duties And Responsibilities. Participate and assist in design and preparation of protocols and case report forms. Generate clinical SOPs, policies, charters, and plans according to US and international guidelines. Participate in the evaluation of pote...
Job Description. Responsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee, this position will serve as support for the clinical study team. Essential Duties And Responsibilities. Participate and assist in design and preparation of protocols and case report forms. Generate clinical SOPs, policies, charters, and plans according to US and international guidelines. Participate in the e...
Responsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee, this position will serve as support for the clinical study team. Essential Duties And Responsibilities. Participate and assist in design and preparation of protocols and case report forms. Generate clinical SOPs, policies, charters, and plans according to US and international guidelines. Participate in the evaluation of pote...
Job Description. Allen Spolden is actively recruiting for a Director of Quality. This is a perm (Direct Hire) opportunity. Relocation assistance will be provided. Location: Gulfport, MS (100% onsite is required.). Work Schedule: M-F, flexible start. Salary: Dependent on experience. Job Summary. The Director of Quality is responsible for developing, implementing, and maintain a cGMP Quality System to meet the requirements of 21CFR210, 21CFR211, Re...
