Career

We are employee driven company. We believe our strength is our people. If you are ready to take challenges, turn opportunities into success and dream to step the ladder of success then please email us your resume in pdf or doc format on careers@ancillarie.com

Job Postings

Biostatistics
Clinical Data Management
Medical Writing
Pharmacovigilance

  • Biostatistics
    • Remote Consultant Principal Biostatistician (1 position- ON, Canada):

    Ph.D in Statistics/Biostatistics with minimum 10+  years of experience. Experience working IND stage clinical trials for Pharma/Biotech industry. Expertise in Expertise in statistical methodologies such as predictive modelling, mixed effects models, adaptive designs, Bayesian statistics, etc. Experience interacting with FDA and Regulatory agencies on statistical issues. Knowledge of FDA and ICH regulations and guidelines Strong computing skills in SAS or other programming languages. Effective written and verbal communication skills.

  • Clinical Data Management
    • Associate Clinical Data Processor (1 position- Mumbai, MH, India):

    Bachelor’s Degree in any stream or Final Year Appeared with zero to one year of experience in performing data entry activities. Experience in MS Office; additional Certification in MS-Office or Microsoft Office Specialist (MOS) certification will be an asset. Ability to read, write and speak in English; English proficiency certificate and ability to read, write and speak in regional Language will be an asset.

    • Associate Clinical Data Manager ( 2 positions- Mumbai, MH, India):

    Bachelor’s Degree (Science, Pharmacy, Life science), or Final Year Appeared with zero to one year of experience in Clinical Data Management. Experience in MS Office; additional Certification in MS-Office or Microsoft Office Specialist (MOS) certification will be an asset. Ability to read, write and speak in English; English proficiency certificate and ability to read, write and speak in regional Language will be an asset.

    • Associate Clinical Database Programmer (1 position-Mumbai, MH, India):

    Bachelor’s Degree (Science, Pharmacy, Life science, computer application), or Final Year Appeared with zero to one year of experience in Clinical Data Management. Experience in MS Office, database programming MS-Access, programming in Visual Basic ; additional Certification in MS-SQL, MS-Office or Microsoft Office Specialist (MOS) certification will be an asset. Ability to read, write and speak in English; English proficiency certificate and ability to read, write and speak in regional Language will be an asset.

    • Clinical Data Manager (1 position-Mumbai, MH, India):

    Bachelor’s Degree (Science, Pharmacy, Life science), with minimum Four to five years of experience in Clinical Data Management. Experience in MS Office; additional Certification in MS-Office or Microsoft Office Specialist (MOS) certification will be an asset. Familiarity with Medical Terminology; additional Medical Terminology Certificate will be an asset. Experience working in study conduct and closed phase for EDC and Paper based clinical trial.

    • Remote Consultant Clinical Data Manager (1 position-ON, Canada):

    Bachelor’s Degree (Science, Pharmacy, Life science), with minimum Four to five years of experience in Clinical Data Management. Experience in MS Office; additional Certification in MS-Office or Microsoft Office Specialist (MOS) certification will be an asset. Familiarity with Medical Terminology; additional Medical Terminology Certificate will be an asset. Experience working in study conduct and closed phase for EDC and Paper based clinical trial.

    • Clinical Database Programmer (1 position- Mumbai, MH, India):

    Bachelor’s Degree (Science, Pharmacy, Life science, Computer Application), with minimum Four to five years of experience in Clinical Data Management. Experience in MS Office; additional Certification in MS-Office or Microsoft Office Specialist (MOS) certification will be an asset. Familiarity with Medical Terminology; additional Medical Terminology Certificate will be an asset. Experience in performing CRF annotation and creating DB specification. Knowledge of CDISC standards is an asset. Experience working with at least one Clinical Data Management system  (Inform , RAVE , Medrio) .

  • Medical Writing
    • Remote Consultant Senior Medical Writer (2 Position,MH-India):

Master’s Degree (Pharmacy, Medicine), with minimum 7 to 9 years of experience in Medical Writing writing of regulatory clinical documents such as clinical trial reports, investigators brochures, summary documents and other documents covering interpretation and documentation of clinical data.  Preferably you have developed your scientific research methods and scientific writing skills and you master written and spoken English at a professional level, and you have a flair for, and a genuine interest in scientific communication.

  • Pharmacovigilance
    • Remote Consultant Principal Safety Associate: (1 position, Canada/India)

Master’s degree (medical, nursing, or pharmacy school or college/university) in the biological or life sciences. 10+ years’ experience in a drug safety surveillance setting within the pharmaceutical/biopharmaceutical industry. Comfortable interacting with small or large groups/across departments/ writing and providing presentations. Can influence/persuade others and has good negotiation skills. Ability to solve complex problems and provide creative solutions. Ability to build teams and consensus.

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