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Senior Cra

0-2 years
Not Disclosed
10 March 24, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Clinical Research Associate -

Updated: March 10, 2025
Location: India-Asia Pacific - IND-Home-Based
Job ID: 24006813

Description
Senior Clinical Research Associate
Syneos Health® is a fully integrated biopharmaceutical solutions organization designed to accelerate customer success by translating clinical, medical affairs, and commercial insights into impactful outcomes.

Why Syneos Health:

  • Career development and progression opportunities.

  • Supportive and engaged line management.

  • Technical and therapeutic area training with peer recognition and total rewards programs.

  • Commitment to a Total Self culture where authenticity is valued.

  • Diversity of thoughts, backgrounds, and perspectives to create an inclusive work environment.

Job Responsibilities:

  • Conducts site qualification, initiation, interim monitoring, management, and close-out visits, ensuring compliance with regulatory, ICH-GCP, and protocol guidelines.

  • Evaluates site performance and escalates serious issues to the project team while developing corrective actions.

  • Verifies informed consent process and maintains subject/patient confidentiality.

  • Assesses factors impacting subject safety and clinical data integrity, addressing protocol deviations and pharmacovigilance concerns.

Clinical Monitoring/Site Management Plan (CMP/SMP):

  • Assesses site processes and performs source document reviews.

  • Ensures clinical data in the case report form (CRF) is accurate through source verification.

  • Resolves queries using appropriate techniques and provides guidance to site staff.

  • Verifies compliance with electronic data capture (EDC) requirements.

Investigational Product (IP) Compliance:

  • Manages IP inventory, reconciliation, storage, and security.

  • Verifies appropriate dispensing and administration of IP per protocol.

  • Ensures GCP/local regulatory compliance for IP relabeling, import, and return.

Document Management:

  • Reviews and reconciles the Investigator Site File (ISF) with the Trial Master File (TMF).

  • Ensures archiving of essential documents in accordance with local regulations.

  • Documents site activities through confirmation letters, follow-up letters, trip reports, and communication logs.

Project Management:

  • Tracks project scope, budgets, and timelines to meet deliverables.

  • Acts as a liaison with project site personnel to ensure compliance with requirements.

  • Prepares for and attends Investigator Meetings and sponsor meetings.

Audit Readiness and Compliance:

  • Provides guidance for audit preparation and follow-up actions.

  • Trains and mentors junior CRAs and may conduct training sign-offs.

Real World Late Phase (RWLP) Responsibilities:

  • Supports sites from identification to close-out.

  • Conducts chart abstraction and data collection.

  • Collaborates with Sponsors, Medical Science Liaisons, and local staff.

  • Develops country-level informed consent forms and collaborates with RWLP Regulatory teams.

Qualifications:

  • Bachelor’s degree or RN in a related field or equivalent education, training, and experience.

  • Strong knowledge of GCP/ICH Guidelines and applicable regulations.

  • Good computer skills with the ability to adopt new technologies.

  • Excellent communication, presentation, and interpersonal skills.

  • Ability to travel up to 75% regularly.

Additional Information:

  • Syneos Health has contributed to 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products, and over 200 Studies across 73,000 Sites and 675,000+ Trial patients in the past 5 years.

  • Tasks, duties, and responsibilities listed are not exhaustive and may be modified as required.