Company: Fortrea
Fortrea Official Website
Location: Bangalore
Employment Type: Full-time
Requisition ID: 262282
Application Type: External Clinical Operations Role
1. Role Overview
The Clinical Research Associate II is responsible for site monitoring and clinical trial oversight to ensure patient safety, data integrity, and compliance with regulatory standards.
This role involves frequent travel to clinical sites and hands-on execution of monitoring activities across all phases of clinical trials, in alignment with ICH-GCP and sponsor requirements.
2. Core Responsibilities
A. Site Monitoring & Clinical Trial Oversight
Conduct all types of site visits:
Pre-study visits
Site initiation visits (SIV)
Routine monitoring visits
Close-out visits
Ensure sites comply with protocol and regulatory requirements
Verify investigator and site staff training records
B. Patient Safety & Compliance
Ensure proper informed consent process is followed
Verify adherence to protocol and regulatory requirements
Track and follow up on Serious Adverse Events (SAEs)
Ensure protection of study participants throughout trial lifecycle
C. Data Integrity & Source Verification
Perform 100% Source Data Verification (SDV)
Conduct eCRF reviews and query resolution
Ensure accuracy, completeness, and consistency of clinical trial data
Identify deviations and initiate corrective actions
D. Regulatory & Documentation Management
Maintain and review essential regulatory documents
Ensure completeness of eTMF and site files
Ensure audit readiness at all times
Track investigational product (IP) accountability and storage
E. Clinical Operations & Coordination
Assist with investigator recruitment and site selection (where applicable)
Support study teams with operational planning and execution
Participate in investigator meetings and project teleconferences
Use CTMS and eClinical systems for tracking and documentation
F. Reporting & Communication
Prepare accurate and timely trip reports
Present training during site initiation visits
Communicate findings clearly to study teams and sponsors
Support training of new CRAs and co-monitoring activities
3. Required Qualifications
Education
University/college degree in life sciences or allied health field
Nursing certification or equivalent clinical qualification acceptable
Equivalent clinical research experience may substitute education
Experience
Minimum 2+ years in clinical monitoring (CRA experience)
Experience in site monitoring, SDV, and clinical trial execution
Strong understanding of ICH-GCP and clinical trial processes
Regulatory & Technical Knowledge
ICH-GCP guidelines
Local regulatory requirements
SAE reporting and tracking processes
Clinical trial documentation and audit readiness
CTMS and eClinical systems
4. Core Skills
Clinical & Technical Skills
Site monitoring and SDV
Clinical trial operations
Adverse event tracking (SAE handling)
eCRF and CTMS system usage
Protocol compliance verification
Operational Skills
Time and travel management (60% travel requirement)
Risk-based monitoring awareness
Study documentation and reporting
Organizational and planning ability
Soft Skills
Strong attention to detail
Communication and interpersonal skills
Problem-solving in field environments
Ability to work independently in a matrix structure
Negotiation and stakeholder management
5. Key Skill Areas (From JD Keywords)
Clinical Monitoring & Site Management
Clinical Research & Trials Execution
Data Integrity & Source Verification
Pharmacovigilance (SAE tracking)
Regulatory Compliance (ICH-GCP)
eClinical Systems (CTMS, eTMF)
6. Organizational Context
This role sits within a Contract Research Organization (CRO) environment, directly supporting sponsor-led clinical trials. It plays a critical role in ensuring real-world clinical trial execution at investigative sites, bridging hospitals, investigators, and sponsor teams.
7. Role Positioning in Career Ladder
Compared to the other roles you shared:
Entry-level operational clinical role in hands-on trial execution
Feeds into:
Senior CRA → Lead CRA → Clinical Trial Manager → Clinical Sciences Trial Leader
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Hajipur | Patna |Kerala :
Kannur | Kochi | Malappuram | Thiruvananthapuram | Trivandrum |Pondicherry (Puducherry) :
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Ranchi |Sikkim :
Rangpo |India :
Remote, India | Siliguri |Illinois :
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Frank Scottile Blvd |Missouri :
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Berlin |Baden-Wurttemberg :
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Frankfurt | Harveysburg |Germany :
Germany | GErmany |Lower Saxony :
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Saarbrucken |Switzerland :
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Belgrade | Serbia |Hungary :
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Bulgaria | Vedant |Denmark :
Copenhagen | Denmark |Europe :
Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
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Istanbul | Turkey |Norway :
Norway | NOrway |Romania :
Romania |Belgium :
Wavre |Tipperary :
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Brinny | Ringaskiddy |Carlow :
Carlow |Republic of Ireland :
Cork | Dublin | Limerick | Waterford |Ulster :
Donegal |Meath :
Dunboyne |Dún Laoghaire :
Dún Laoghaire |Galway :
Galway |County Dublin :
Swords |Republic of China :
Beijing |China :
China | Quarry Bay |Liaoning :
Dalian |Zhejiang :
Hangzhou |Tokiyo :
Osaka | Tokyo |Shanghai Sai :
Shanghai Shi |Hubei :
Wuhan |Capital of Netherland :
Amsterdam |North Brabant :
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Leiden |Netherlands :
Netherlands |Remote Australia :
Arkansas | Remote Australia |New South Wales :
Ballina | Sydney |Republic of Western Australia :
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Queensland |Melbourne :
South Yarra |United Kingdom :
England | Harlow | Leeds | London | Maidenhead | Salt Lake City | Stevenage | Stirling | United Kingdom |North Yorkshire :
Harrogate |South Yorkshire :
Sheffield |Oxfordshire :
Witney |Ontario :
North York | Richmond Hill | Australia | Mississauga | Renfrew | Uxbridge |Canada :
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Argentina | Peru |Brazil :
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Auckland |New Zealand :
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Remote Korea |Republic of Korea :
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Springville | Nairobi | Leinster | Tulsa | Ireland | Zaragoza | Hammond | Melbourne | Medan | Manipal | Remote - Africa | Hungary | Remote - Europe | Bountiful | Minnesota | Bishop | Slovakia | Riga | Remote - Middle East | Xzagreb | Switzerland | Lenexa | Green Way | Remote - South America (Latin Americal) | French | Remote, USA | Blue Bell | Belgium | Remote | Thailand | Victoria | Faridabad | McFarland | Lousiana | Texas | Castlebar | Regulatory Labeling Manager (NA and LATAM Only) |Republic of Colombia :
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King Abdullah Economic City | Jeddah | Najran | Rabigh | Khulais | Riyadh |Kuala Lumpur :
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Kyiv |Lima Region :
Lima |France :
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Niš |Bohemia :
Prague |Chile :
Santiago |Bosnia and Herzegovina :
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Warsaw |