Scientific Research Associate Analyst

symplr

1d • $65,000 - $75,000

About The Position

The Scientific Research Associate Analyst is responsible for systematically researching, identifying, and summarizing clinically founded evidence using health technology assessment methodology. Performs work focused in Precision Medicine. Prepare reports addressing complex topics in precision therapeutics, molecular tests, or overviews of the appropriateness of genetic testing for a particular indication.

Requirements

• Graduate level training (MS, MSc, MPH, PhD or ScD) or equivalent expertise in clinical genetics or health sciences
• Demonstrated English language writing skills, particularly pertaining to health and medical topics
• Excellent analytical skills
• Proficiency with basic computer applications (specifically Microsoft Office 2010 or above— Word, Excel, and PowerPoint); ability to manage files and work within a digital environment comfortably
• Interest in client and prospect needs
• Ability to work well independently and meet deadlines and contribute in a team setting
• Proactive, effective communication and interpersonal skills necessary to collaborate in cross-functional teams as well as to engage as part of a remote team
• Passionate about helping clients improve healthcare outcomes

Nice To Haves

• For Precision Medicine focus area: Master’s or PhD in human genetics, genetic counseling, or other specialty related to precision medicine
• Clinical experience in a genetics laboratory and/or genetic counseling
• Prior experience in performing HTAs or systematic reviews
• Knowledge of the healthcare industry
• Experience with references managers
• Skill in performing comprehensive literature searches of all appropriate databases
• Skill in performing health technology assessment and/or systematic review

Responsibilities

• Gather and synthesize content to identify and scope individual report topics and develop a report preparation protocol
• Design and conduct a comprehensive search that is pertinent to selection criteria using keywords and cross-references
• Determine and implement appropriate and systematic study selection criteria for inclusion of studies in reports
• Analyze biomedical literature and write reports using Microsoft Office software or AuthorIT (content management software) using systematic review methodology and Hayes conventions; identify, organize, and synthesize data, extract data into evidence tables, critically appraise evidence, and assign a Hayes Rating where appropriate; write with scientific rigor and clarity; and manage deadlines for reports; work with other groups and individuals to complete the report, including content editors, technical editors, and digital publishing support
• Maintain thorough records including scoping/protocol development, bibliographic database searching, and citation management, and all decisions related to study selection
• Perform other duties as assigned

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level