Is the Contractor, Clinical Trial Associate position at Syndax Pharmaceuticals fully remote?

Yes, this Contractor, Clinical Trial Associate position at Syndax Pharmaceuticals is a remote position. The role is available for candidates in United States.

Is this a full-time or part-time Contractor, Clinical Trial Associate role?

This is a contract Contractor, Clinical Trial Associate position at Syndax Pharmaceuticals.

How do I apply for the Contractor, Clinical Trial Associate position at Syndax Pharmaceuticals?

You can apply for this Contractor, Clinical Trial Associate position by clicking the "Apply Now" button on this page, which will take you to Syndax Pharmaceuticals's application portal.

Contractor, Clinical Trial Associate at Syndax Pharmaceuticals

United States

Position Description: The Contractor, Clinical Trial Associate will work with Clinical Operations team to support the conduct of clinical trials.  The Clinical Trial Associate may provide support for various clinical trials and may manage certain aspects of the clinical trials.  The Clinical Trial Associate will partner with the Clinical Project Managers and Clinical Trial Managers to ensure studies are completed on time, within budget, and in compliance with SOPs, FDA regulations and ICH/GCP guidelines.  Responsibilities and Duties: <ul> <li>Maintain the Trial Master Files (TMF): Responsible for the on-going management of the TMF for assigned clinical trials. This is inclusive of receipt, review, QC, tracking and filing of all documents per the Syndax SOPs required within the conduct of assigned clinical trials.</li> <li>Ensure TMF is inspection ready</li> <li>Provide TMF metrics to internal and external stakeholders</li> <li>Work closely with all cross functions to adhere to the trial master oversight plan</li> <li>Assist with the development and maintenance of tracking tools for patient recruitment, site ramp-up, monitoring visits and site payments.</li> <li>Work with Clinical Operations to assist in the oversight of CROs, as appropriate, to ensure the successful conduct of clinical trials, including attending and participating in Clinical Trial Working Groups as needed.</li> <li>Assist in reviewing monitoring visit reports to ensure proper conduct and oversight as needed.</li> <li>Review site-specific Informed Consent Forms</li> <li>Track site feasibility questionnaires</li> <li>Assist in the planning of various meetings and events for the Clinical Operations Team</li> <li>Reconcile invoices to their corresponding contracts and budget and assist with investigator site payments.</li> <li>Prepare and manages study communications including newsletters and study updates</li> <li>Records, prepares and distributes meeting minutes for assigned clinical trials or as designated by the VP of Clinical Operations.</li> <li>Work closely with Clinical Trial Managers to assist with preparation of all external and internal documentation for assigned trials to ensure it's completed in accordance with GCP regulatory requirements and consistent with the study protocol.</li> </ul>  Minimum Requirements: <ul> <li>Two years’ experience in Veeva Vault</li> <li>Two or more years’ experience in clinical operations- experience in both a CRO and Sponsor setting desired.</li> <li>Knowledge of FDA regulatory requirements and ICH/GCP guidelines essential</li> <li>Demonstrated efficiency in partnering with CROs and vendors</li> <li>Computer proficiency (Veeva TMF, Word, Excel, PowerPoint, Smart Sheet)</li> <li>Work proactively and efficiently in a fast-paced, high change environment</li> <li>Excellent written and oral communication skills</li> <li>Outstanding organization skills</li> <li>Bachelor's degree desired, preferably in a science or healthcare related discipline</li> </ul> Location: While our corporate headquarters are located in New York City, this position is open to candidates from any location with a preference for east coast locations.   About Syndax: Syndax Pharmaceuticals is a commercial-stage biopharmaceutical company advancing innovative cancer therapies. Highlights of the Company’s pipeline include a menin inhibitor for R/R acute leukemia and a monoclonal antibody that blocks the CSF-1 receptor for chronic graft-versus-host disease. Fueled by our commitment to reimagining cancer care, Syndax is working to unlock the full potential of its pipeline and is conducting several clinical trials across the continuum of treatment. For more information, please visit <a href="https://nam11.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.globenewswire.com%2FTracker%3Fdata%3DrCAVnMToulbfZv6WH-CwoAOkYpm_Zgk-73ncBiDnf3nIX6R3CClytFbSaCr38-uyz2V0Pk2LozJ-QwSHS6X0TSUH8ksfUpHQPeejdWP_C3UjPSPN4YE9QerowK_ttD5hTVuH8uxQf-KWvDu3st-pcTRGKMXkcww7XNvGOSAxWWaYf_a20AAx9mxGY2DmomHwds4yYDrO-O7Rqb06KaQXIA%3D%3D&data=05%7C02%7Cdconrad%40syndax.com%7C62774ab8166749c0867908dd8cbc307e%7C2fe7898cf9fb418abd81f98ad3cc1894%7C0%7C0%7C638821462075993064%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&sdata=FjZavjSrcbWTQEJ4Yx2dMavm1j9K7BMpigGW%2BzeBFmA%3D&reserved=0">www.syndax.com/</a> or follow the Company on <a href="https://nam11.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.globenewswire.com%2FTracker%3Fdata%3Dwx7WvIgknTbUrdGoBqJDyfmnZv7YjpVw69FBz4FPIpAMSR6p-6G-1eEU1NN_PYKazoY9Fnu0i7tbtlt6kOsyUg%3D%3D&data=05%7C02%7Cdconrad%40syndax.com%7C62774ab8166749c0867908dd8cbc307e%7C2fe7898cf9fb418abd81f98ad3cc1894%7C0%7C0%7C638821462076005193%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&sdata=VPfzxHWAdn51W%2FJvK0R9ElN%2BSta428MFv8%2BffmvPXhg%3D&reserved=0">X </a>and <a href="https://nam11.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.globenewswire.com%2FTracker%3Fdata%3DutvMIwxxtq4HsdhXEGUK-9naWAlyxWDCUVWYC1-zQ7-ItUe3nCkvSO7W03MncrtTIB7B3XLR46VSIPMFMm-7GX7qEUXdHT_eLp5paIn9pm95jkReA1YyJUpBBv81rWV-kVoUvHDOXdizDQ9AMsN2mvY404a1ud9AxuKCGhyI1NNyy6VaAhUaJ-PuUcADGMJQCYBQ4RES4q0WgT9UuJZR6Egj0ets0CXh885IchTskB4%3D&data=05%7C02%7Cdconrad%40syndax.com%7C62774ab8166749c0867908dd8cbc307e%7C2fe7898cf9fb418abd81f98ad3cc1894%7C0%7C0%7C638821462076017518%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&sdata=L%2FdGgGGvBw0KMvBqm25ukL5ubX38Yz8cifjS0A%2F1fEA%3D&reserved=0">LinkedIn</a>. Syndax Pharmaceuticals is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law. #LI-Remote

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Remote Opportunity

Contractor, Clinical Trial Associate

Join Syndax Pharmaceuticals as a mid professional working remotely from United States. Explore the role, benefits, and apply in one place.

Contractor, Clinical Trial Associate

Syndax Pharmaceuticals

Contract

2 months ago

Position Description: The Contractor, Clinical Trial Associate will work with Clinical Operations team to support the conduct of clinical trials. The Clinical Trial Associate may provide support for various clinical trials and may manage certain aspects of the clinical trials.

United States

Engineering

Mid

Veeva Vault

Clinical Operations

TMF Management

+5 more

Job Description

Position Description:

The Contractor, Clinical Trial Associate will work with Clinical Operations team to support the conduct of clinical trials. The Clinical Trial Associate may provide support for various clinical trials and may manage certain aspects of the clinical trials. The Clinical Trial Associate will partner with the Clinical Project Managers and Clinical Trial Managers to ensure studies are completed on time, within budget, and in compliance with SOPs, FDA regulations and ICH/GCP guidelines.

Responsibilities and Duties:

Maintain the Trial Master Files (TMF): Responsible for the on-going management of the TMF for assigned clinical trials. This is inclusive of receipt, review, QC, tracking and filing of all documents per the Syndax SOPs required within the conduct of assigned clinical trials.
Ensure TMF is inspection ready
Provide TMF metrics to internal and external stakeholders
Work closely with all cross functions to adhere to the trial master oversight plan
Assist with the development and maintenance of tracking tools for patient recruitment, site ramp-up, monitoring visits and site payments.
Work with Clinical Operations to assist in the oversight of CROs, as appropriate, to ensure the successful conduct of clinical trials, including attending and participating in Clinical Trial Working Groups as needed.
Assist in reviewing monitoring visit reports to ensure proper conduct and oversight as needed.
Review site-specific Informed Consent Forms
Track site feasibility questionnaires
Assist in the planning of various meetings and events for the Clinical Operations Team
Reconcile invoices to their corresponding contracts and budget and assist with investigator site payments.
Prepare and manages study communications including newsletters and study updates
Records, prepares and distributes meeting minutes for assigned clinical trials or as designated by the VP of Clinical Operations.
Work closely with Clinical Trial Managers to assist with preparation of all external and internal documentation for assigned trials to ensure it's completed in accordance with GCP regulatory requirements and consistent with the study protocol.

Minimum Requirements:

Two years’ experience in Veeva Vault
Two or more years’ experience in clinical operations- experience in both a CRO and Sponsor setting desired.
Knowledge of FDA regulatory requirements and ICH/GCP guidelines essential
Demonstrated efficiency in partnering with CROs and vendors
Computer proficiency (Veeva TMF, Word, Excel, PowerPoint, Smart Sheet)
Work proactively and efficiently in a fast-paced, high change environment
Excellent written and oral communication skills
Outstanding organization skills
Bachelor's degree desired, preferably in a science or healthcare related discipline

Location: While our corporate headquarters are located in New York City, this position is open to candidates from any location with a preference for east coast locations.

About Syndax:
Syndax Pharmaceuticals is a commercial-stage biopharmaceutical company advancing innovative cancer therapies. Highlights of the Company’s pipeline include a menin inhibitor for R/R acute leukemia and a monoclonal antibody that blocks the CSF-1 receptor for chronic graft-versus-host disease. Fueled by our commitment to reimagining cancer care, Syndax is working to unlock the full potential of its pipeline and is conducting several clinical trials across the continuum of treatment. For more information, please visit www.syndax.com/ or follow the Company on X and LinkedIn.

Syndax Pharmaceuticals is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.

#LI-Remote

Skills

Veeva Vault

Clinical Operations

TMF Management

FDA Regulations

ICH/GCP guidelines

CRO Oversight

Patient Recruitment Tracking

Informed Consent Review

Ready to Apply?

Join Syndax Pharmaceuticals today

Posted 2 months ago

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