Immediate need for a talented Rheumatology Review Group Eligibility Liaison. This is a 12 Months Contract opportunity with long-term potential and is located in Giralda Farms, NJ(Onsite).

Please review the job description below and contact me ASAP if you are interested.

Job ID : (phone number removed)

Pay Range : $40 - $48 / hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location).

Key Responsibilities :

Responsible for ensuring site participants in screening are ready for RRG review through site communication and clinical / study data coordination and tracking.

Manage communication of participant status with the RRG via email and REL progress tracker.

Completes training and remains current with RRG processes to respond to a site’s questions related to Screening Eligibility

Work closely with the sites to ensure completion of all activities within 15 days from the screening visit and contact the country specific CTMs for support if required.

Oversees and tracks site screening activities in the REL Progress tracker to ensure completion of lab results, data entry and query resolutions within the 28-day screening timeline.

Reviews lab data to determine if lab retests may be required and / or any exclusionary labs are present; contacts sites / CTM / lab / RRG as needed.

Liaises with GTM and CTMs as needed to prompt site responsiveness.

Determines when participants are ready for RRG eligibility review and notifies the RRG.

Works with sites and CTMs (when needed) to enable timely resolution of RRG queries.

Tracks RRG Eligibility eCRF queries to resolution; issues re-queries as needed.

Communicates with sites throughout the RRG eligibility review process to ensure timely decisions can be made (including but not limited to communication regarding status of lab results, RRG queries, disagreement with RRG decisions, etc.).

Facilitates email communication between sites and the Lead RRG Coordinator and RRG Lead Reviewer.

Facilitates virtual meetings between sites and the RRG and / or Efficacy and Eligibility

Adjudication Committee when necessary.

Key Requirements and Technology Experience :

Bachelor’s degree preferred.

2 to 5 years of experience in clinical research or equivalent (industry, academic or study site experience is acceptable).

Proficient knowledge of GCP / ICH, drug development process and clinical trial operations.

Extensive proficiency in Microsoft Office software and Electronic Data Capture (e.g., RAVE)

Must have strong interpersonal skills, be a team player and be willing to work in an environment where individual initiative and accountability to the team are required.

Excellent verbal, written and communication skills.

Detail-oriented with a commitment to quality.

Proficient in medical terminology with the ability to assimilate technical information

quickly.

Proficient knowledge of the disease area(s) is preferred.

Adaptable / Flexible - willing and able to adjust to multiple demands and shifting

priorities as well as an ability to meet day-to-day challenges with confidence and

professionalism.

Our client is a leading Pharmaceutical Industry and we are currently interviewing to fill this and other similar contract positions.

If you are interested in this position, please apply online for immediate consideration.

Pyramid Consulting, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

Last updated : 2024-05-20