At a glanceSummarised by Seekless from the posting.
Must have7
Strong clinical research and study start-up experience.
Excellent problem-solving, communication, presentation, and stakeholder management skills.
Ability to work independently, prioritize multiple tasks, and make decisions in ambiguous situations.
Strong knowledge of CTMS, eTMF, TMF, and Microsoft Office tools.
Experience working in global, matrix, and multicultural environments.
High attention to detail, quality focus, and commitment to achieving project timelines.
Excellent English skills (oral and written).
Nice to have1
Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or another health-related field (or equivalent experience) is preferred.
Skills
CTMS
eTMF
TMF
Microsoft Office
When our values align, there’s no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world’s health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we’re committed to making a difference.
About the role
The Initiation Clinical Research Associate (iCRA) is responsible for leading and executing all study start-up, pre-SIV, activation, and protocol amendment activities from site identification through site activation and maintenance. Acting as the primary contact for assigned sites, the iCRA manages regulatory submissions, site readiness, document quality, and activation timelines while ensuring compliance with sponsor, regulatory, and company requirements.
Responsibilities
Key responsibilities include:
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Managing site start-up activities from feasibility and qualification through activation.
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Building strong relationships with investigators and site staff.
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Preparing, reviewing, negotiating, and executing regulatory and site documents, including CDAs, ICFs, translations, and amendments.
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Coordinating submissions and approvals with IRBs/IECs, Ministries of Health, and Regulatory Authorities.
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Developing and tracking activation strategies, timelines, and regulatory plans.
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Maintaining high-quality documentation in CTMS, eTMF, and TMF systems, ensuring First Time Quality (FTQ).
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Identifying, resolving, or escalating site issues and risks related to activation, recruitment, compliance, training, and data quality.
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Supporting sites with study system access, training requirements, and readiness activities.
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Ensuring sites remain audit- and inspection-ready throughout the study lifecycle.
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Maintaining compliance with ICH-GCP guidelines, local regulations, sponsor requirements, and Parexel SOPs.
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Collaborating cross-functionally to achieve project milestones and deliverables while proactively communicating progress, risks, and issues.
Required Skills and Experience:
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Strong clinical research and study start-up experience.
•
Excellent problem-solving, communication, presentation, and stakeholder management skills.
•
Ability to work independently, prioritize multiple tasks, and make decisions in ambiguous situations.
•
Strong knowledge of CTMS, eTMF, TMF, and Microsoft Office tools.
•
Experience working in global, matrix, and multicultural environments.
•
High attention to detail, quality focus, and commitment to achieving project timelines.
•
Excellent English skills (oral and written).
Education: Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or another health-related field (or equivalent experience) is preferred.