Senior Clinical Trial Associate

🔥 1 minute ago

🇺🇸 United States – Remote

💵 $95k - $120k / year

⏰ Full Time

🟠 Senior

👻 Ghost score 0%

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Immatics

WebsiteLinkedInAll Job Openings

201 - 500 employees

Founded 2000

🏥 Healthcare

🧬 Biotechnology

💊 Pharmaceuticals

Healthcare • Biotechnology • Pharmaceuticals

Immatics is a biotechnology company focused on developing targeted immunotherapies for cancer patients, particularly in treating solid tumors. The company combines the discovery of cancer immunotherapy targets with the development of specific T cell receptors to enable a robust immune response. Immatics' pipeline includes Adoptive Cell Therapies and TCR Bispecifics, and it collaborates with global leaders in the pharmaceutical industry. The company's mission is to advance its therapies to improve the lives of cancer patients, and it maintains a strong commitment to innovation in immunotherapy technologies.

📋 Description

• Support clinical trial start-up, activation, maintenance, and closeout activities • Collect and manage essential study documents • Maintain and perform quality reviews of trial information within CTMS, eTMF, and other clinical systems • Partner with internal teams, CROs, vendors, and investigative sites to drive study execution and resolve operational issues • Support inspection and audit readiness through accurate, complete, and compliant trial documentation • Coordinate trial-related meetings, documentation reviews, approvals, and administrative activities • Manage purchase orders, invoices, investigator payments, and study-related financial tracking • Prepare, review, and quality-check study documents, reports, trackers, and investigator site files • Support TMF and ISF maintenance, reconciliation, and quality oversight • Coordinate training assignments, system access, and compliance tracking for study teams • Monitor site issues, action items, and data query resolution to support study milestones • Track and follow up on outstanding EDC queries and facilitate timely resolution • Facilitate site communications, including study updates, newsletters, and distribution of trial materials • Contribute to risk identification, issue escalation, process improvements, and inspection readiness efforts • Support development of SOPs, work instructions, guidance documents, and training materials • Assist with remote and on-site monitoring activities, as appropriate

🎯 Requirements

• Bachelor’s degree in life sciences, nursing, or a related field • 4+ years’ working experience in the clinical research area in the Pharmaceutical or Biotech industry with ICH-GCP knowledge, or equivalent • Strong problem-solving skills with the ability to analyze issues, identify root causes, and implement effective solutions • Self-motivated and able to work independently in a fast-paced environment • Strong understanding of clinical trial processes and interconnected operational workflows • Continuous improvement mindset with a passion for enhancing processes and team effectiveness • Demonstrated ability to drive innovation and share expertise across teams • Must be authorized to work in the United States without the need for current or future sponsorship • Successful completion of background check, reference checks, and pre-employment drug screening, where permitted by applicable law

🏖️ Benefits

• Health, Dental, and Vision Insurance • 4 weeks of vacation, granted up front each year and prorated for first and last year of employment • 12 company paid holidays • 7 days of sick time • 100% employer-paid life insurance up to 1x annual salary, up to one hundred thousand dollars • 100% employer-paid short- and long-term disability coverage • 401(k) with immediate eligibility and company match • Partially paid parental leave for eligible employees • Additional voluntary employee-paid benefits and services, including accident, hospital indemnity, and critical illness insurance, identity theft protection, and pet insurance

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