Clinical Research Associate II, Client Based

🔥 0 minutes ago

🇮🇳 India – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 10%

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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Syneos Health

WebsiteLinkedInAll Job Openings

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 • Evaluate site and site staff performance and recommend site-specific actions • Communicate or escalate serious issues and develop action plans • Verify informed consent, subject confidentiality, safety, clinical data integrity, protocol compliance, and pharmacovigilance issues • Conduct source document review and verify clinical data in case report forms • Resolve queries remotely and on-site and guide site staff • Support clinical study data review, capture, and electronic data capture compliance • Manage investigational product inventory, reconciliation, storage, dispensing, administration, and related regulatory requirements • Review Investigator Site Files and reconcile them with Trial Master Files • Document monitoring activities through letters, reports, logs, and project documents • Support subject/patient recruitment, retention, and awareness strategies • Track observations, site status, and action items • Manage site-level activities, communications, budgets, timelines, deliverables, and project objectives • Act as liaison with study site personnel and ensure assigned sites and project staff are trained and compliant • Attend investigator, sponsor, global monitoring, project, 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, collaborate with sponsor affiliates and local staff, train junior staff, identify out-of-scope activities, and suggest potential sites

🎯 Requirements

• Minimum 3 years of onsite monitoring experience in Global Clinical Trials • 1–2 years of Oncology experience preferred • Experience in Neuroscience, Haematology, Cardiovascular, or Rare Disease preferred • 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 75% on a regular basis

🏖️ Benefits

• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition • Total rewards program • Inclusive culture • Remote opportunity