Senior Clinical Trial Associate

Rapport Therapeutics•Boston, MA

6h•Hybrid

About The Position

Rapport Therapeutics is dedicated to developing precision neuromedicines with the potential for fewer side effects, aiming to improve the lives of patients and their families. The company's innovative scientific platform focuses on Receptor Associate Proteins (RAPs), which are crucial in regulating neuronal receptor assembly and function. This approach seeks to revolutionize small molecule therapies. Rapport's lead program, RAP-219, is in clinical trials for focal epilepsy, neuropathic pain, and bipolar disorder. The company emphasizes a mission-driven culture, valuing science, teamwork, and a commitment to patient improvement. As a Senior Clinical Trial Associate, the role involves being a key player in managing clinical studies, ensuring they stay on track, supporting the team, and contributing to bringing innovative treatments to patients.

Requirements

Bachelor's degree in life sciences or healthcare related field
3+ years' experience in a clinical trial support position
Strong computer skills including knowledge of Excel, Word, PowerPoint and Outlook
Solid understanding of the responsibilities and needs of other functions in a clinical trial
Proven ability to work independently and effectively handle multiple priorities in a fast-paced environment
Ability to multitask and flex across projects as priorities and deadlines shift
Ability to maintain confidentiality of proprietary information
A team player that takes initiative and is proactive

Nice To Haves

Experience in Biotech or Pharma strongly preferred

Responsibilities

Coordinates and tracks the distribution and subsequent retrieval of clinical documents, including but not limited to protocols, protocol amendments, IBs, ICF's, monitoring visit reports, etc.
Supports maintenance of inspection-ready Trial Master File (TMF) according to ICH-GCP and company SOPs
Perform quality checks on the study TMF with oversight of study COL
Assists in the preparation of study related documents, i.e., ICF, clinical trial tools and templates, etc.
May coordinate and track clinical trial equipment and supplies
Review and track vendor invoices against contracts with oversight of study COL
Coordinates and tracks administrative aspects of contract execution and PO generation
Supports the trial team to produce and distribute study newsletters
Supports collection and updating of clinical trial insurance
Supports posting of all agreed clinical trials to publicly available websites
Assists with various supportive trial activities, i.e., meeting management including agenda distribution and minute taking, internal database maintenance, study team contact list, etc.
May support additional ad-hoc activities as agreed with the study COL