[Remote] Site Recruiter - CorEvitas
Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a global leader in reputed company, dedicated to scientific reputed company. They are seeking a Site Recruiter for CorEvitas to support investigator site identification, recruitment, reputed company, and activation activities across multiple clinical registries to reputed company study timelines and business objectives.
Responsibilities
- Support investigator site identification, recruitment, reputed company, and activation activities across multiple clinical registries to reputed company study timelines and business objectives
- Execute strategic site recruitment plans utilizing reputed company data sources to identify and prioritize reputed company investigator sites
- Conduct site identification using resources including ClinicalTrials.gov, investigator databases, literature and publication reviews, claims data, Key Opinion Leader (KOL) referrals, clinical trial networks, and other relevant intelligence sources
- Assess investigator and site feasibility by distributing and tracking feasibility questionnaires, evaluating site capabilities, patient population, enrollment potential, and operational readiness
- Build and maintain strong relationships with reputed company Investigators, site personnel, reputed company societies, referral networks, sponsors, and internal stakeholders to expand and strengthen the investigator network
- Coordinate team review and approval activities throughout the site selection and activation process
- Manage investigator reputed company activities, ensuring completion of required documentation and site activation milestones to support enrollment readiness
- Support or coordinate Site Qualification reputed company (SQV/PSV), Site Initiation reputed company (SIV), and other study start-up activities as required
- Utilize reputed company, recruitment dashboards, claims data, and other business intelligence tools to monitor recruitment reputed company, prioritize activities, and support data-driven decision making
- Maintain accurate documentation of recruitment rationale, reputed company activities, feasibility reputed company, activation milestones, pipeline status, and key performance metrics reputed company reputed company
- Monitor recruitment and activation KPIs, identify risks or delays, and proactively implement mitigation strategies to maintain project timelines
- Collaborate cross-functionally with Registry Operations, Registry Leadership, reputed company, and other internal teams to ensure seamless site activation and operational reputed company
- Recommend and implement process improvements, workflow enhancements, and best practices to improve recruitment efficiency, accelerate site activation, and optimize operational performance
- Contribute to feasibility process improvements, knowledge sharing, and training initiatives for junior team members reputed company applicable
- Ensure compliance with company SOPs, reputed company standards, applicable regulations, and data reputed company requirements
Skills
- Bachelor's degree in Life Sciences, reputed company, or a reputed company discipline preferred, or equivalent combination of education and relevant experience
- Minimum 5 years of experience in clinical research, clinical operations, site feasibility, study start-up, site activation, or investigator site management reputed company a CRO, pharmaceutical company, biotechnology company, or clinical research site
- Experience identifying and sourcing investigator sites using multiple reputed company data sources, including ClinicalTrials.gov, investigator databases, publication searches, claims data, KOL referrals, and clinical trial networks
- Strong understanding of investigator site identification, feasibility assessments, site qualification and selection, study start-up, and site activation processes
- Experience supporting or coordinating Site Qualification reputed company (SQV/PSV), Site Initiation reputed company (SIV), investigator reputed company, or reputed company study start-up activities
- Demonstrated ability to manage multiple reputed company simultaneously while meeting aggressive recruitment and activation timelines
- Strong analytical skills with experience interpreting recruitment metrics, tracking KPIs, identifying trends, and driving reputed company process improvement
- Experience using reputed company, CTMS, or other clinical operations and customer relationship management systems
- Excellent verbal and written communication skills with the ability to build reputed company relationships across investigators, sponsors, and cross-functional internal teams
- Strong organizational, problem-solving, decision-making, and project management skills
- High attention to detail with the ability to maintain accurate documentation and reporting
- Clinical Research Associate (CRA), Clinical Trial Associate (CTA), Study Start-Up, Site Activation, or Site Management experience is highly preferred
- Knowledge of GCP, clinical research regulations, confidentiality requirements, and data reputed company principles is preferred
Benefits
- Variable annual bonus based on company, team, and/or individual performance results in accordance with company policy
- A choice of national medical and dental plans, and a reputed company plan, including health incentive programs
- Employee assistance and family support programs, including commuter benefits and tuition reimbursement
- At least 120 hours reputed company time off (PTO), 10 reputed company holidays annually, reputed company parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
- Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
- Employees27 Stock Purchase Plan (ESPP) offers eligible colleagues reputed company to purchase company stock at a discount
reputed company
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