Screening Deputy Lead

Quotient Sciences • Miami, FL

6d

About The Position

Assist the Screening Manager in tracking performance of screening activities for prospective research volunteers. Responsible for assisting for day-to-day volunteer marketing and recruitment activities to meet study enrollment timelines. Responsible for ensuring volunteer recruitment practices are fair and ethical. Support Screening Manager by providing cover and assistance with screening set up for upcoming studies/cohorts. To comply & adhere to GCP guidelines and regulations as required of this role. To ensure study data is collected to a high quality in accordance with Good Clinical Practice (GCP) standards. To ensure subject safety at all times.

Requirements

• Associate degree (preferred) or high school graduate
• At least 2 years’ experience of working in a health-related environment, preferably clinical research
• Fluent in English/Spanish
• Computer proficient and ability to navigate through various specialized computerized systems
• Demonstration of digital skills in social media communications
• Good understanding of the latest online marketing concepts, strategy, and best practice
• Demonstration of initiating, delivering, and analyzing advertising campaigns for recruitment of volunteers
• Excellent organizational skills and problem-solving abilities
• Ability to perform multiple tasks and prioritize effectively to meet required deadlines
• Excellent communication and interpersonal skills
• Detail oriented and self-directed

Responsibilities

• Work with Screening Manager, PI, and Clinical Lead to understand demands/strategy for studies to ensure advertising plans meet the requirements
• Responsible for assisting the Screening Manager for updating the company volunteer recruitment website in advance of the screening start date
• Posting of social media for volunteer recruitment (Facebook, Instagram and Twitter etc.) and responding to comments on all platforms (as applicable)
• Preparation of Admission Lists, Screening Logs as needed
• Thoroughly read and understand protocols and train screening staff on protocol prior to start of recruitment or screening
• Ensures ethical and adequate recruitment and screening of prospective research volunteers for studies
• Explains research study and obtains proper informed consent. Ensures consents are completed prior to the performance of any screening activities
• Obtains medical histories and documents findings according to SOPs, protocol specific requirements and Good Clinical Practice
• Assists with the performance and/or scheduling of all screening procedures required by protocol
• Assists in obtaining clinical laboratory specimens and shipping to the appropriate laboratory as needed
• Reviews abnormal results of screening tests with the Investigators and alerts volunteers of results, which need further medical evaluation
• Reviews completed screening charts for completeness and conformity with protocol requirements. Reports and documents any clinical results or compliance issues which would lead to study exclusion
• Ensures that screen failures charts are properly archived in a timely manner
• Assists with other duties as assigned
• Liaise with the medical team to assess volunteer suitability for inclusion on the database where required
• Respond to volunteer queries, involving other staff as appropriate in order to provide the best response

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: Associate degree