Offer summary

Qualifications:

Minimum of 2 years of relevant clinical trial experience or healthcare background., Bachelor's degree or equivalent in a scientific discipline, or RN certification., Proficiency in Word, PowerPoint, and Excel., Knowledge of FDA, EMEA regulations, ICH guidelines, and GCPs..

Key responsibilities:

Monitor study progress and track study activities.

Coordinate patient enrollment and communicate with site personnel.

Maintain and QC Trial Master Files and study documentation.

Provide regular updates and support administrative tasks for clinical trials.

Job description

COMPANY BACKGROUND

Akero Therapeutics is a clinical stage biopharmaceutical company focused on discovering and developing transformational treatments for patients with serious metabolic diseases marked by high unmet need. Our current focus is on advancing our lead program efruxifermin (EFX) to provide a powerful new treatment for patients with MASH(metabolic dysfunction-associated steatohepatitis).

We are a team of problem solvers dedicated to pursuing bold scientific approaches to build a brighter future for patients. Our diverse skill sets and backgrounds, desire to learn from each other and collaborative spirit breed a culture where everyone feels inspired to bring their best thinking to work, and to bring out the best in others.

Job Summary

The Clinical Trial Management Associate (CTMA) is a key member of Clinical Operations and will closely partner with the Senior Clinical Trial Manager.

Job Responsibilities

Accountable for study level tracking as assigned by the Clinical Project Manager; e.g. monitor visit tracking and sample tracking.
Ensures patient enrollment activities are conducted in a timely manner and is comfortable communicating with site personnel.
Provides study level information to enable accurate and efficient supply of clinical product to the sites.
Acts as QC of Trial Master Files; creates, maintains, and closes out TMFs; is key in set up, conduct, and close out of ancillary services.
Accountable for ensuring that agendas for meetings are clear and distributed in advance; takes comprehensive and precise minutes for internal and external meetings.
Proactively identifies potential operational challenges and in collaboration with senior team members provides solutions to ensure study execution remains on track.
May participate in review of data listings and preparation of interim/final clinical study reports, including resolving data discrepancies.
Provides regular study updates to the appropriate internal stakeholders.
Maintains internal Clinical Operations databases and document repositories.
Performs administrative duties in a timely manner as assigned.
Assist with administration of invoice reconciliation, scoping, and change orders, for clinical trial operations.
Adheres to Clinical Operations processes and SOPs

Qualifications

At least 2+ years of relevant experience and a BS or BA in a relevant scientific discipline OR
At least 2+ years of experience and an RN (2 or 3 year certificate)

Technical Requirements and Skills

Relevant clinical trial experience in the pharmaceutical or health care industry or equivalent
Excellent attention to detail, verbal, written, interpersonal and presentation skills are required
Must be familiar with routine medical/scientific terminology
Must be familiar with Word, PowerPoint, and Excel
Must have working knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials
Must be able to participate in departmental or interdepartmental strategic initiatives under general supervision
High energy level, personal productivity, creativity and commitment.
Team-player with desire to work in a fast-moving, dynamic start-up environment.
This position is for remote work but may require domestic or international travel as required (valid travel documents must be obtainable).

Compensation

Below is the pay range for this position that we reasonably expect to pay. Individual compensation is based on a number of factors including, experience, education and skill set, and geographic location. This range is for the San Francisco Bay Area, California location and may be adjusted to the labor market in other geographic areas.

Pay range: $103,000 - $114,000 per annum

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