Senior Clinical Data Manager - Remote

Posted Yesterday

All others

Full Time

USA

$145,000 - $160,000/year

Clinical Data Management

Good Clinical Practice (GCP)

Overview

The Senior Clinical Data Manager (Sr. CDM) is a strategic and hands-on leader responsible for overseeing end-to-end data management activities across multiple global clinical trials, ensuring the integrity, accuracy, and completeness of clinical trial data.

In Short

Lead data management for Phase II/III trials.
Ensure compliance with Good Clinical Practice (GCP).
Provide strategic input into study designs and data collection.
Maintain and implement data management plans (DMPs).
Ensure accuracy and completeness of trial data.
Collaborate with cross-functional teams and external partners.
Oversee CRO data management deliverables.
Drive process improvement and innovation in data management.
Proficient in EDC platforms and data programming languages.
Manage multiple priorities in fast-paced environments.

Requirements

Bachelor’s degree in Life Sciences or related field; Master’s preferred.
10+ years of experience in clinical data management.
Proven track record in leading global clinical trials.
Deep understanding of regulatory requirements and CDISC standards.
Proficiency with EDC platforms like Medidata Rave.
Strong leadership and project management skills.
Exceptional problem-solving and analytical abilities.
Skilled communicator for cross-functional collaboration.
Vendor oversight experience.
Technical proficiency in SAS, SQL, or other data programming languages.

Benefits

Competitive salary range of $145,000 - $160,000.
Opportunities for professional growth and development.
Innovative work environment focused on rare respiratory diseases.
Collaboration with experienced professionals in the field.
Engagement in impactful clinical trials.
Potential for remote work flexibility.
Dynamic and supportive company culture.
Access to cutting-edge technologies and methodologies.
Comprehensive health benefits.
Participation in a mission-driven organization.

A.P

Avalyn Pharma

Avalyn Pharma is a biotechnology company focused on developing innovative, targeted inhaled therapies for rare respiratory diseases, particularly idiopathic pulmonary fibrosis (IPF) and progressive pulmonary fibrosis (PPF). With a recent oversubscribed $175M Series C financing, Avalyn is advancing its clinical-stage portfolio, which includes inhaled formulations of FDA-approved antifibrotics such as pirfenidone and nintedanib. The company aims to improve patient outcomes by providing inhaled alternatives that are better tolerated than traditional oral medications, thereby addressing the significant side effects that affect 30-50% of patients. Avalyn's lead product, AP01, has shown promising results in clinical studies, demonstrating efficacy and safety in patients with pulmonary fibrosis.

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