Clinical Document Agent

Job not on LinkedIn

🔥 0 minutes ago

🇮🇳 India – Remote

⏰ Full Time

🟢 Junior

✨ Agent

👻 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

• Create documentation forms for clinical projects • Draft patient files and convert raw data into electronic format while following established procedures and processes • Create subject files, review templates, adhere to timelines, correct mistakes before transcription, and follow up on client comments • Generate electronic documentation forms for the clinic • Suggest and order subject meals for the length of a study and perform follow-up • Digitalize raw study data transferred by the Clinical Study Manager • Calculate final blood volumes for each subject per study • Ensure subjects have correct washout-period dates • Perform peer review of team work • Help resolve problems related to the work being performed • Train new team members • Contact internal and external collaborators to obtain documents needed to meet timeframes • Perform other assigned clinical tasks • Ensure activities comply with applicable corporate and divisional policies, standard operating procedures, and operating guidelines

🎯 Requirements

• Bachelor / Master’s degree in a Life Sciences • 1 to 3 years of experience • Work Shift timing: 2 PM to 11 PM IST (2nd Shift) • Understanding of Clinical Trial documentation • Phase 1 experience is must • Knowledge of Investigator Site Files (ISF) • Must have experience in Document QC • Must have experience in Excel, creating forms and creating source documentation in Excel • Knowledge of Adobe and computer skills • Excellent communication skills • Ability to coordinate with cross-functional global teams • Ability to understand requirements and translate them into documentation • Good computer skills, especially Microsoft Word and Excel • Excellent written and spoken communication, presentation, and interpersonal skills • Experience in regulatory context will be considered an asset

🏖️ Benefits

• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition • Total rewards program • Inclusive culture • Flexible remote work arrangement (Remote (Pre-Approved))