Clinical Document Agent

🔥 2 hours ago

🇮🇳 India – Remote

⏰ Full Time

🟢 Junior

✨ Agent

👻 Ghost score 10%

What it means: the chance that no one is really hiring for this job.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.

Apply Now

Find Similar Remote Jobs

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 by reviewing templates, adhering to timelines, correcting mistakes before transcription, and following up on client comments • Generate electronic documentation forms for the clinic • Suggest and order subject meals for the length of a study and perform necessary follow-up • Digitalize raw study data transferred by the Clinical Study Manager • Calculate final blood volumes for each subject per study • Ensure each subject has the correct dates for their washout period • Perform peer review of team work • Help resolve work-related problems • Train new team members • Contact internal and external collaborators to obtain documents needed to meet timeframes • Perform other assigned clinical tasks • Ensure compliance with 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 adobe, computer skills • Excellent Communication skills • Ability to coordinate with cross-functional global teams • Ability to understand requirements and translate them into documentation • Candidates with TMF Lead experience may also be considered • Must demonstrate good computer skills especially in the utilization of Microsoft Word and Excel • Excellent communication, presentation, interpersonal skills, both written and spoken • Experience in regulatory context will be considered an asset • Equivalent experience, skills, and/or education will also be considered

🏖️ Benefits

• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition • Total rewards program • Inclusive culture • Reasonable accommodations when appropriate

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume