Clinical Trial Associate

Arrowhead Pharmaceuticals•San Diego, CA

6h•$60,000 - $80,000

About The Position

Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing. Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. The Position The Clinical Trial Associate (CTA) provides administrative support to the Clinical Operations Department. The primary purpose of the position is to facilitate efficient clinical trial planning and execution.

Requirements

1 year of experience in similar industry position
Pharmaceutical or biotechnology environment experience andvalued but not mandatory
Ability to multi-task and prioritize effectively with input from manager or Study Lead
Proficient interpersonal, verbal and written communication skills
Ability to work effectively independently and in a collaborative team environment
Basic software skills (MS-Outlook, Word, Excel, DocuSign)
Ability to perform Key Duties and Responsibilities in a timely manner and with minimal supervision

Nice To Haves

4-year college degree preferred
Basic understanding of Good Documentation Practice (GDP) and ICH-GCP
Ability to readily identify and categorize essential document types as defined by ICH E6 for submission to TMF
Proficiency in Veeva eTMF

Responsibilities

Set up and maintain clinical trial master files (hardcopy and/or electronic format) in compliance with SOPs
Develop and maintain study tools including trackers, spreadsheets, and filing systems for various studies
Preparation and revision of Purchase orders; follow-up with vendors on invoice issues
Plan and coordinate department meetings and activities, as requested, including handling logistics, preparation of agendas, distribution of meeting materials
Assist COMs with drug and ancillary supply management
Assist with preparation of study related documents and presentations
Assist Associate Director with Clin Ops SOP/WI team training
Assist COMs with eTMF filing and reconciliation as needed
Attend department meetings and record minutes as requested
Facilitate initiation of and track study agreements and contracts for COMs
QC study related documents (Protocols, ICFs, Study Plans, etc.)
May function as a liaison between clinical vendors on behalf of COMs
Manage off-site document storage and recall as applicable
Any other study related tasks assigned by Clinical Operations Team members