Meridian Research Solutions is seeking experienced Clinical Research Associates (CRAs) to support pharmaceutical, biotechnology, and medical device clients across global clinical trials. Our CRAs are qualified through education, industry training, and hands-on experience to ensure patient safety, data integrity, and ICH-GCP compliance at every monitoring visit. Key Responsibilities: Conduct site selection, initiation, monitoring, and close-out visits Verify source documents and ensure data accuracy in EDC systems Identify and document protocol deviations and non-compliance issues Collaborate with Clinical Trial Managers and site coordinators to resolve action items Ensure inspection-readiness of site files and Trial Master File documentation Qualifications: Bachelor's degree in life sciences, nursing, or related field 2+ years of on-site monitoring experience (CRO or pharma) In-depth knowledge of ICH-GCP guidelines and FDA/EMA regulations Willingness to travel up to 70% (for on-site roles) Therapeutic area expertise in Oncology, Cardiology, CNS, or Rare Diseases preferred

Meridian Research Solutions is seeking Clinical Project Managers to lead global clinical trials from study start-up to close-out. Our CPMs oversee cross-functional teams, manage vendor relationships, and ensure studies are delivered on time, within budget, and in compliance with regulatory requirements. Key Responsibilities: Develop and manage study timelines, budgets, and resource allocation Lead cross-functional team meetings and track study progress against milestones Manage vendor performance (CROs, central labs, imaging providers) Identify and mitigate study risks and implement contingency plans Ensure inspection-readiness of all study documentation Qualifications: Bachelor's degree (advanced degree preferred) 5+ years of clinical research experience, including 2+ years in project management PMP certification or equivalent is highly desirable Strong knowledge of ICH-GCP and regulatory submission requirements Experience with Phase III global trials preferred

Meridian Research Solutions is seeking a Senior Recruitment Consultant to join our internal talent acquisition team. In this role, you will source, screen, and place clinical research professionals (CRAs, CTMs, CRCs, Regulatory Specialists) with our pharmaceutical, biotech, and CRO clients. Key Responsibilities: Source and engage passive candidates using LinkedIn Recruiter, job boards, and networking Conduct competency-based interviews and assess GCP knowledge Manage full recruitment lifecycle from requisition to offer acceptance Build and maintain relationships with hiring managers at client organizations Achieve placement targets across permanent and contract roles Qualifications: 3+ years of recruitment experience (clinical research or life sciences preferred) Proven track record of placing CRA or CTM roles Familiarity with ICH-GCP guidelines and clinical trial operations Strong negotiation and relationship management skills Experience with applicant tracking systems (ATS)

Meridian Research Solutions is seeking Clinical Trial Managers to oversee the operational execution of clinical trials. Our CTMs serve as the primary point of contact between sponsors, CROs, and investigative sites, ensuring seamless study conduct from first patient in to database lock. Key Responsibilities: Oversee day-to-day study operations and site management activities Track patient enrollment, data entry, and query resolution metrics Coordinate with CRAs on monitoring visit schedules and follow-up actions Review monitoring reports and escalate site performance issues Ensure studies are inspection-ready at all times Qualifications: Bachelor's degree in life sciences or related field 4+ years of clinical research experience, including CRA and CTM experience Strong understanding of ICH-GCP and clinical trial regulations Experience with EDC systems and CTMS platforms Ability to manage multiple studies simultaneously

Meridian Research Solutions is seeking Clinical Trial Assistants to provide administrative and operational support to Clinical Trial Managers and project teams. Our CTAs are essential to maintaining organized, inspection-ready Trial Master Files and facilitating smooth study conduct. Key Responsibilities: Assist with study document preparation, distribution, and tracking Maintain and update the Trial Master File (TMF) and investigator site files Coordinate meeting logistics, agendas, and minutes for study team meetings Track regulatory submissions and ethics committee approvals Support CTMs with site correspondence and action item tracking Qualifications: Associate or Bachelor's degree preferred 1+ years of clinical research or administrative experience Familiarity with TMF structure and ICH-GCP guidelines Proficient in Microsoft Office (Word, Excel, PowerPoint, Outlook) Highly organized with strong attention to detail

Meridian Research Solutions is seeking a Business Development Manager to expand our clinical research staffing and consulting services. You will identify, pursue, and secure new partnerships with pharmaceutical companies, biotechnology firms, CROs, and medical device organizations. Key Responsibilities: Identify and qualify new business opportunities within clinical research Develop and deliver sales presentations and proposals to prospective clients Negotiate master service agreements (MSAs) and rate cards Attend industry conferences and networking events Collaborate with recruitment teams to ensure service delivery alignment Qualifications: 5+ years of business development or sales experience (CRO/pharma/clinical staffing) Existing network of clinical research decision-makers Understanding of clinical trial operations and staffing needs Excellent presentation, negotiation, and closing skills Willingness to travel for client meetings and conferences

Meridian Research Solutions is seeking Clinical Data Associates to support data management activities for global clinical trials. Our CDAs are responsible for reviewing clinical data, issuing queries, and ensuring database accuracy in compliance with regulatory standards. Key Responsibilities: Review and clean clinical data in EDC systems (e.g., Rave, Veeva, InForm) Issue and resolve data queries with investigative sites Perform data validation checks per data management plan Assist with database lock activities and data transfer specifications Maintain data management documentation and metrics Qualifications: Bachelor's degree in life sciences, computer science, or related field 2+ years of clinical data management experience Proficiency with EDC systems and CDISC standards Understanding of ICH-GCP and regulatory requirements for data Strong analytical and problem-solving skills

Meridian Research Solutions is seeking a TMF Manager to oversee the quality, completeness, and timeliness of Trial Master File documentation for global clinical trials. You will ensure that all study documents meet regulatory requirements and are inspection-ready at all times. Key Responsibilities: Develop and implement TMF plans and document filing timelines Oversee TMF content management in eTMF systems (e.g., Veeva, TransPerfect) Conduct TMF quality reviews and reconciliation activities Ensure compliance with ICH-GCP and sponsor TMF specifications Train study team members on TMF processes and standards Qualifications: Bachelor's degree in life sciences or related field 5+ years of clinical research experience, including TMF management Strong knowledge of ICH-GCP and regulatory documentation standards Experience with eTMF systems and TMF metrics reporting Meticulous attention to detail and organizational skills

Meridian Research Solutions is seeking a Manager, Document Management to lead clinical document control activities. You will oversee the creation, review, approval, storage, and distribution of clinical study documents, ensuring readiness for regulatory submissions and inspections. Key Responsibilities: Manage document control processes for clinical study documentation Oversee document version control, approval workflows, and archiving Ensure compliance with SOPs, ICH-GCP, and regulatory guidelines Coordinate with clinical teams to prepare submission-ready document packages Lead document management system upgrades and user training Qualifications: Bachelor's degree (advanced degree preferred) 7+ years of clinical document management experience Experience with electronic document management systems (eDMS) Strong knowledge of regulatory submission requirements (FDA, EMA) Proven leadership and process improvement skills