Search Remote Jobs

CRA I – Sponsor Dedicated, Oncology, Neurology

🔥 2 minutes ago

🏈 Ohio – Remote

infoinfo

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

Where this job comes from

Posted on Syneos Health's careers page, not through a job board

First seen by Remote Rocketship 2 minutes ago

Logo of Syneos Health

Syneos Health

10,000+ employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.

📋 Description

• Perform site qualification, site initiation, interim monitoring, site management and close-out visits, on-site or remotely • Ensure regulatory, ICH-GCP/GPP and protocol compliance • Evaluate site and staff performance and recommend site-specific actions • Escalate serious issues and develop action plans with guidance • Verify informed consent, subject/patient confidentiality, safety and clinical data integrity • Assess site processes under the Clinical Monitoring/Site Management Plan • Conduct source document review and medical-record review • Verify clinical data in case report forms and electronic data capture compliance • Resolve queries remotely and on site within agreed timelines • Use hardware and software for clinical project data review and capture • Manage investigational product inventory, reconciliation, storage, dispensing and related compliance as applicable • Review Investigator Site Files and reconcile them with the Trial Master File • Document monitoring activities through letters, trip reports, communication logs and project documents • Support subject/patient recruitment, retention and awareness strategies • Track observations, status and action items to resolution • Manage site-level activities and communications to meet project objectives, deliverables and timelines • Act as liaison with project site personnel and ensure site-team training and compliance • Attend investigator, sponsor, global monitoring and clinical training meetings • Support audit readiness, audit preparation and follow-up actions • For Real World Late Phase: support sites throughout the study lifecycle, perform chart abstraction and data collection, and collaborate with sponsor affiliates, medical science liaisons and local country staff

🎯 Requirements

• Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience • Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements • Good computer skills and ability to embrace new technologies • Excellent communication, presentation and interpersonal skills • Ability to manage required travel of up to 30% on a regular basis • Must comply with site requests for medical and other personal information required for facility access in the US • For Real World Late Phase: knowledge of local requirements for real world late phase study designs

🏖️ Benefits

• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition and total rewards program • Company car or car allowance may be included • Medical, Dental and Vision health benefits • Company match 401k • Eligibility to earn commissions/bonus based on company and individual performance • Flexible paid time off (PTO) • Sick time

Apply Now

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Similar Jobs

🔥 40 minutes ago

ICON plc

10,000+ employees

💼 Consulting

🏥 Healthcare

📦 Logistics

Clinical Research Associate monitoring sponsor-dedicated cardio and obesity clinical trials for ICON Strategic Solutions. Conducting site visits, ensuring protocol compliance, and maintaining clinical data quality.

🔥 40 minutes ago

ICON plc

10,000+ employees

💼 Consulting

🏥 Healthcare

📦 Logistics

Clinical Research Associate monitoring sponsor-dedicated cardio and obesity clinical trials for ICON. Conducting site visits, ensuring protocol compliance, and maintaining clinical data integrity.

🔥 1 hour ago

ICON plc

10,000+ employees

💼 Consulting

🏥 Healthcare

📦 Logistics

Clinical Research Associate monitoring clinical trials for ICON Strategic Solutions. Ensuring protocol compliance, data integrity, and patient safety across study sites.

🔥 3 hours ago

GondolaBio

11 - 50

🏥 Healthcare

💼 Consulting

🏭 Manufacturing

Senior CRA/Associate CTM supporting GondolaBio’s genetic-disease clinical trials from start-up through closeout. Overseeing sites, CROs, vendors, data, and regulatory compliance remotely.

🇺🇸 United States – Remote

💵 $110k - $120k / year

💰 $300M Venture Round - GondolaBio on 2024-08

⏰ Full Time

🟠 Senior

🧪 Clinical Research

🔥 3 hours ago

Elevar Therapeutics

11 - 50

🧬 Biotechnology

💊 Pharmaceuticals

🏥 Healthcare

Senior Clinical Trial Manager overseeing global clinical trial planning, vendors, compliance, and execution. Supporting Elevar Therapeutics’ growing biotech operations, preferably in oncology.

🇺🇸 United States – Remote

💵 $170k - $187k / year

💰 $20M Venture Round - Elevar Therapeutics on 2018-07

⏰ Full Time

🟠 Senior

🧪 Clinical Research

Developed by Lior Neu-ner. I'd love to hear your feedback — Get in touch via DM or support@remoterocketship.com
Follow Remote Rocketship on LinkedInFollow Remote Rocketship on InstagramFollow Remote Rocketship on FacebookFollow Remote Rocketship on TikTok