Contract – Clinical Research Coordinator

Job not on LinkedIn

🔥 0 minutes ago

🌲 North Carolina – Remote

🌲 North Carolina – Remote

⏳ Contract/Temporary

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 12%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Science 37

WebsiteLinkedInAll Job Openings

501 - 1000 employees

🏥 Healthcare

💊 Pharmaceuticals

🔬 Science

💰 $200M Post-IPO Equity on 2021-10

Healthcare • Pharmaceuticals • Science

Science 37 is making the promise of virtual trials the new reality. By engaging with patients from the comfort of their own home, we provide access to patients who can never be reached by traditional site-based models. We have proven to enroll faster, retain patients at a higher rate, and reach a more representative population. Science 37 has conducted more decentralized, interventional trials than any other company, using an expansive, in-house network of telemedicine investigators and home-health nurses, who are supported by the industry’s most comprehensive, fully integrated, decentralized clinical trial platform.

📋 Description

• Recruit, enroll, and conduct follow-up of study participants in clinical trials under the supervision of the Principal Investigator and Project Manager • Coordinate trial participation according to protocols, SOPs, GCP/ICH guidelines, FDA regulations, and other applicable regulations • Participate in clinical trial activities from study start-up through planning, execution, and closure • Attend investigator, project, and department meetings and trainings; lead as needed and prepare meeting minutes • Participate as temporary Project Manager for smaller studies when needed • Determine participant eligibility with study investigators • Screen potential participants, present trial details, participate in informed consent, and enroll participants • Support development, review, and distribution of protocols, consent forms, study instructions, manuals, guidelines, and study tools • Coordinate patient care, provide medication-administration education when applicable, and maintain investigational drug accountability • Review participant condition changes, adverse events, concomitant medications, protocol compliance, and response to study drug; document findings • Collect, document, enter, and report data accurately and promptly; schedule and participate in monitoring and audits • Maintain knowledge and compliant execution of assigned research protocols and regulatory requirements • Maintain consent forms, case report forms, SAEs, source documents, and regulatory documents in the ISF • Coordinate clinical research project logistics and support enrollment and retention goals • Participate in training and educate personnel and vendors regarding clinical research • Collaborate with Project Managers, investigators, vendors, sponsors, sites, and multidisciplinary teams • Provide process-improvement solutions and assist with implementation • Maintain participant confidentiality under HIPAA and provide a safe research environment • Mentor and train other CRCs and support the CRC team • For hybrid trials: act as site/Sponsor point of contact, develop project and communication plans, and support site study execution

🎯 Requirements

• Bachelor’s degree (preferred) or minimum two-year college degree, or an equivalent combination of education, training, experience, and demonstrated skills • Advanced degree preferred but not required • Minimum of 5 years of pharmaceutical-sponsored clinical research experience is required or commensurate education, training, and experience within the clinical research field • ACRP (CCRC) or SoCRA (CCRP) certification highly desired • Experience working with patients in a HIPAA regulated environment • Knowledge of Good Clinical Practice (GCP) and applicable regulatory requirements • Medical and scientific knowledge preferred • Excellent time management and organizational skills; ability to manage multiple tasks • Attention to detail and accuracy • Ability to collaborate with cross-functional team members • Expertise in trial management and clinical research • Expert knowledge of FDA regulations and GCP guidelines • Strong written and verbal communication and presentation skills • Proficiency with MS Office and Google Suite applications • Expertise using proprietary software • Ability to adapt to a rapidly changing environment and work in a decentralized team environment • Ability to communicate in English, verbally and in writing • May require extended or unusual work hours based on research requirements and business needs

🏖️ Benefits

• Potential to convert to Full Time after 6 months • Up to 20% travel, as needed, for project team meetings, client presentations and other professional meetings/conferences • Equal opportunity/affirmative action employment