Onsite/Hybrid - Clinical Research Support Specialist

Description

Description

Onsite/Hybrid- Clinical Research Support Specialist

Our rapidly growing clinical research team is looking to hire a qualified Medical Assistant certified candidate for the full-time position of Clinical Research Support Specialist. 

SUMMARY:

The Clinical Research Support Specialist position is responsible for reviewing the clinical eligibility of patients using our proprietary technology, patient Medical History and the Inclusion/Exclusion criteria of the enrolling clinical trials at each of our clinical research sites. This position is also responsible to engage with those patients identified to communicate their clinical research options and work with our Clinical Coordinator teams to schedule subsequent screening visits. This position is engaged in all recruiting/prescreening and site operations support projects being conducted at assigned centers in order to ensure compliance with protocols and overall clinical objectives.

WHO WE ARE:

ObjectiveHealth is a clinical research company that uses proprietary technology to:

• Increase patient access to research trials within our community
• Provide physicians with enhanced care options for current patients, and
• Deliver superior clinical research enrollment metrics to Pharma sponsors
• Everything we do at ObjectiveHealth is focused on helping patients. We’re offering them more regular, specialized care. We’re addressing a need. We’re making innovative, new treatment options available. We’re changing lives through an innovative approach to research and patient care. But what sets us apart isn’t our methodology, our science, or even our decades of experience in the medical field. It’s our people. People who view medicine in a new way – one that’s aimed at developing groundbreaking treatment options for patients. People who share a passion for advancing our unique brand of patient care.

We invite you to be part of the innovation we’re working toward.

WHO YOU ARE:

• Medical Assistant certification required
• A lover of patient interaction and skilled at providing patient care
• A team player with a bias for action and an attitude that takes personal responsibility
• Skilled in all aspects required for conducting an IRB approved clinical trial protocol: identification, screening, randomization, and enrollment of patients, conducting clinic visits, etc.
• Skilled at performing and assisting with direct patient care activities: consenting patients, physical assessments, blood draws, medication administration, ECG, etc.
• Possess an acute attention to detail for clean data entry, regulatory compliance, site visits, study set-up and maintenance, and protocol adherence
• An expert communicator with the goal of fostering relationships between the research team, PIs, Sponsors, Monitors, and others
• Not easily distracted: You have the ability to stay focused while running different protocols, resolving and submitting IRB responses and audit findings, tracking AE and SAE events, and maintaining eSource material for assigned studies

KNOWLEDGE, SKILLS AND ABILITIES:

• Technologically advanced: Ability to learn new software systems easily and previous experience working on multiple systems
• Experience handling inbound and outbound calls with patients
• Ability to maintain professionalism, patience and efficiency in communicating with patients
• Gastrointestinal or research experience preferred 
• Knowledge of electronic medical record systems and EDC systems preferred
• Knowledge of CTMS systems preferred
• Must have a sense of urgency and set priorities
• Identify and resolve problems effectively and efficiently
• Excellent communication and organizational skills for managing workflow and follow-up
• Ability to demonstrate reliability and maintain confidentiality

WHAT SUCCESS LOOKS LIKE FOR THIS ROLE

• Taking ownership of their assigned studies and patients
• Communicating promptly and effectively with leadership and coworkers when you have a question or see something that needs correction
• Showing up on time, every time
• Learning and using the technologies we provide to enhance your day-to-day progress

BENEFITS:

Competitive compensation, 401(k) with Company match, a clear career pathway for advancement within the Company, Short- and Long-Term Disability, Health Savings and Flexible Spending Accounts, Health, Dental and Vision insurance Plans, Generous PTO, Paid Holidays, and a wide selection of other voluntary benefits.

Schedule: 8 hour shift

Work Location: Franklin, TN Hybrid 

Requirements

This job requires l