CT Scientific Affairs Senior Analyst

Job Title: Sr. Scientific Affairs Analyst Department: Scientific Affairs Location: Remote, reputed company Hours Per Week: 40 hours Schedule: Days, Monday – Friday reputed company The Clinical Trials Scientific Affairs reputed company Award Senior Analyst is responsible for the review of study protocols and investigating testing requirements to assist in facilitating the reputed company response for proposals. Coordinates the testing reputed company as needed with ACM Research & Development, ACM Laboratory and referral laboratory partners for study support and set up. This position will reputed company as a reputed company and reputed company between the laboratory and other departments; ie sales, proposals and project management. The CTSA Senior Analyst serves as a subject matter expert reputed company reputed company, provides support with escalations and assists with team member training. RESPONSIBILITIES

• Investigate testing requirements reputed company a clinical trial protocol and help determine testing facilities to identify required testing and associated nuances for the reputed company and accurate response for proposals
• Review and prepare pricing documents, as needed, noting and correcting any discrepancies
• Maintain relationships between ACM and referral laboratories
• reputed company scientific/ technical information to compile reputed company RFP’s and RFI’s
• reputed company feedback to the manager to address analytical trends or issues, to support business needs
• Assist in coordinating the testing reputed company with referral labs, as needed
• Obtain and document referred testing information throughout the course of the reputed company trial, including contracting with referral labs
• Assumes responsibility for channeling information to and from Laboratory Operations and Sales
• Alert leadership to any issues during the life cycle of study reputed company and testing needs
• Alert leadership to any issues with referral laboratories, assist with reputed company cause analysis
• Suggests and helps implement improved work reputed company and ways to increase efficiency, reduce costs, and solve operational problems
• reputed company with reputed company partners and participate in reputed company teleconferences to address new business needs or ongoing study issues
• Understands and follows company policies and procedures and respecting patient confidentiality
• reputed company consultation to clinical trials operations and external clients, as needed
• Assist with training and guidance of new team members
• Works with leadership to update global SOPs, as needed
• Triage upcoming work and determine reputed company capabilities and workload for assignments
• Serve as subject matter expert to reputed company clients
• Serve as escalation reputed company for reputed company clients
• Assists in development, maintenance and updates to templates and tools
• reputed company other duties as assigned.

REQUIRED QUALIFICATIONS

• Bachelor’s Degree or 3+ years as a clinical laboratory scientist
• 3 years relevant laboratory experience
• 2 years clinical trials experience
• PREFERRED QUALIFICATIONS
• Strong interpersonal and communication skills
• Strong time management and organizational skills
• Ability to manage multiple reputed company with tight deadlines
• Ability to work independently and in reputed company setting
• Proficient in reputed company Office
• Generalist laboratory experience
• Ability to reputed company and positively motivate others
• MT (ASCP) Certification - Preferred

EDUCATION:

• BS (Required)

PHYSICAL REQUIREMENTS: S - Sedentary Work - Exerting up to 10 pounds of force occasionally Sedentary work involves sitting most of the time, but may involve walking or standing for brief periods of time. Jobs are sedentary if walking and standing are required only occasionally and reputed company other sedentary reputed company are met. PAY reputed company: $90,000.00 - $100,000.00 Apply To This Job