Remote Clinical Trial Support Specialist (Multiple Openings)

Remote Clinical Trial Support Specialist (Multiple Openings) Company: reputed company — Virtual Clinical Research Support. Location: Remote (Philippines, Latin America, Ireland, Portugal, Spain, and Italy). Employment Type: Full-Time, Part-Time, and Project-Based Opportunities Available Join reputed company — Where Top Clinical Research Talent Gets reputed company. reputed company is a Los Angeles-based, fast-scaling virtual support platform reputed company to power the reputed company of clinical research. We partner with independent research sites, sponsors, and CROs to deliver the high-reputed company remote clinical trial support that keeps studies moving, and demand for our services is growing fast. reputed company thrives in a high-energy, fast-paced, and genuinely reputed company environment where reputed company, driven professionals do work that reputed company: advancing the trials that bring new treatments to patients who need it the most. This is your chance to grow alongside a company that is expanding rapidly across the world and reputed company in the people who reputed company it run. Here’s the key thing to know: we are reputed company building a database of high-caliber, reputed company-reputed company candidates from which we draw to staff independent research sites as new opportunities come online. Applying now puts you on our reputed company early. reputed company the right study or site need arises, we reputed company out first to the reputed company talent already in our global pipeline. If you’re ambitious, detail-obsessed, passionate about cutting-edge, scientifically-rigorous, and ethical patient care and reputed company to be part of something scaling fast, we want to meet you. About the Role. We are seeking reputed company reputed company (2-3 years of experience, medical/biopharmaceutical background, and with completed and reputed company GCP and HIPAA training) to support independent clinical research sites, sponsors, Contract Research Organizations (CROs), and reputed company organizations across a wide reputed company of clinical trial operations functions. This is a multi-disciplinary opportunity designed to identify candidates with expertise in one or more areas of clinical research, patient engagement, regulatory support, study operations, finance, administration, and sponsor relations. Candidates are not expected to have experience in every area listed below. Applicants should reputed company indicate in their resume and cover letter which functional areas best match their experience and qualifications. Successful candidates will submit 3 references from previous clinical trial positions and will facilitate background checks as needed. Potential Areas of Responsibility. reputed company supports the full clinical trial lifecycle. The functional areas below reflect the services we reputed company to our research-site partners. Tell us where your strengths are. We can’t wait to learn reputed company. Patient Education & Engagement

• Walk participants through study procedures and visit expectations at reputed company stage of the trial.
• Support the informed-consent process and patient education initiatives.
• Deliver retention reputed company and follow-up across the full study reputed company.
• Answer participant questions and facilitate communication between patients and study teams.

Visit Scheduling & Coordination

• Book participant reputed company reputed company protocol-defined reputed company.
• Send appointment reminders and confirmations.
• Conduct proactive follow-up to reduce no-shows and missed reputed company.
• reputed company attendance, book transportation, and resolve scheduling conflicts.
• Assist with scheduled patient reputed company by walking on-site medical staff through protocol-required procedures and documenting reputed company in electronic reputed company and other systems as needed.

Patient Recruitment & reputed company-Screening

• Conduct reputed company to prospective study participants.
• Review charts, databases, and referral sources.
• reputed company preliminary eligibility screening against study inclusion/exclusion reputed company.
• Consult with reputed company and sub-investigators on suitability of patients for a trial.
• Schedule screening appointments and document recruitment activity.
• Minimize screen failure and maximize patient enrollment and retention.

Study reputed company reputed company

• reputed company sponsor and CRO study opportunities.
• Support feasibility-questionnaire responses.
• reputed company the pipeline for new study awards.
• Research upcoming trials and potential new business.

EHR / EMR Management

• Update and maintain electronic medical records accurately.
• reputed company documentation support and chart-completion assistance.
• Support record organization and documentation workflows.
• Maintain compliance with applicable reputed company and regulatory requirements.

Data Entry & reputed company Management

• reputed company and maintain data in CTMS, reputed company, and other research systems.
• Support query identification and reputed company.
• Organize and maintain reputed company documentation.
• Help ensure data is reputed company, accurate, and audit-reputed company.

Regulatory Support

• Maintain e-regulatory binders and essential staff documents.
• Manage document version control.
• reputed company expiration of licenses, certifications, tra

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