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Cra - Fsp

0-2 years
Not Disclosed
10 March 26, 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

Clinical Research Associate (CRA) - FSP
Location: Bengaluru, India
Company: Parexel


Overview:
As a Clinical Research Associate (CRA) at Parexel, you will play a critical role in accelerating the delivery of treatments to patients. Your primary focus will be ensuring the safety and well-being of patients while maintaining compliance with study protocols. You will work on global projects across a wide range of therapeutic areas, collaborating with diverse teams and gaining valuable professional experience.


Key Accountabilities:

Site Maintenance (from Initiation to Close-out):

  • Serve as Parexel’s direct contact with assigned sites, ensuring adherence to study protocols and addressing site-related issues.

  • Build and maintain relationships with investigators and site staff.

  • Facilitate site access to relevant study systems and ensure compliance with project-specific training.

  • Assess on-site staff assignments, implement corrective actions if needed, and follow up on pending issues.

  • Identify and address deficiencies in documentation, communication, and training.

  • Ensure high-quality data entry and integrity by identifying potential issues and implementing corrective measures.

  • Participate in investigator meetings, audits, and regulatory inspections.

  • Review and approve updated/amended site documentation, including regulatory documents.

  • Monitor recruitment plans, suggesting and implementing strategies for improvement.

  • Conduct on-site qualification and initiation visits, resolving site queries effectively.

  • Conduct remote visits/contacts as required and generate visit/contact reports.

  • Assess and manage test article/study supplies, including accountability and return/destruction.

  • Follow up on site payment status and address delays if needed.

  • Track CRF data entry, query resolution, and SAEs.

  • Conduct on-site study-specific training, perform site facility assessments, and manage non-compliance issues.

Project Management & Compliance:

  • Ensure timely completion of project goals and updates to applicable Clinical Trial Management Systems (CTMS).

  • Collaborate with team members to achieve project milestones and ensure compliance with ICH-GCP guidelines, local regulations, and Parexel SOPs.

  • Review site-level data in systems like CTMS, EDC, IVRS, and SIS.

  • Ensure that assigned sites remain audit and inspection-ready.

  • Delegate and review tasks assigned to the Administrative Support Team, providing performance feedback.

  • Demonstrate a commitment to high-quality work while maintaining a positive and collaborative work environment.

  • Develop subject matter expertise and maintain a working knowledge of project scope, milestones, and budgets.


Skills Required:

  • Strong problem-solving and analytical skills.

  • Ability to work independently and seek guidance when necessary.

  • Advanced presentation and communication skills.

  • Client-focused approach with a professional demeanor.

  • Strong organizational and time management skills to meet project deadlines.

  • Ability to prioritize multiple tasks and resolve unpredictable issues.

  • Proficiency in clinical systems like CTMS, EDMS, and MS Office applications.

  • Willingness to work in a matrix environment and value teamwork.

  • Attention to detail with a sense of urgency.

  • Flexibility to travel extensively and possess a valid driver’s license (if required).


Knowledge and Experience:

  • Prior site management experience or equivalent in clinical research.

  • Solid understanding of clinical trial methodology and associated terminology.


Education Requirements:

  • Degree in biological sciences, pharmacy, or a health-related discipline (preferred).

  • Equivalent nursing qualifications or relevant clinical experience will be considered.