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Clinical Data Management Oppurtunities in Precision for Medicine

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Are you an experienced Clinical Data Associate or Senior Clinical Data Associate looking to take your career to the next level? Precision for Medicine is on the lookout for enthusiastic individuals to join our dynamic team in Bangalore, Karnataka. As a leader in data management services for clinical trials, we are committed to excellence and innovation in the healthcare sector.

About the Role

As a Clinical Data Associate/Senior Clinical Data Associate, you will play a pivotal role in supporting the clinical trial data management process from study initiation to post-database lock. Under direct supervision, you will ensure compliance with our standard operating procedures (SOPs), regulatory guidelines, and study-specific plans.

Key Responsibilities

In this multifaceted position, you will be responsible for:

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  • Data Entry and Quality Control: Perform data entry for paper-CRF studies as needed, and ensure quality control of the data entered.
  • Database Management: Assist in the development, testing, and maintenance of clinical databases, ensuring thorough documentation of the process.
  • Collaboration: Work closely with the Lead Data Manager and team to ensure a seamless workflow and timely completion of tasks.
  • CRF Development: Help develop case report form (CRF) specifications from clinical protocols and coordinate stakeholder feedback.
  • Edit Checks: Specify and create various types of edit checks such as electronic and manual data reviews.
  • Medical Coding: Perform medical coding for clinical trial data, ensuring consistency and adherence to medical logic.
  • Vendor Coordination: Liaise with external data vendors and EDC vendors to support timelines and data-related deliverables.
  • SAS Programming Support: Assist with SAS programming and perform quality control of SAS programs utilized in data management.

Qualifications

To be successful in this role, the ideal candidate should possess the following qualifications:

  • Education: A Bachelor’s degree in a scientific discipline combined with at least 4+ years of experience in data management.
  • Technical Skills: Proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook) and basic knowledge of effective data management practices.
  • Interpersonal Skills: Excellent organizational and communication skills, both written and oral.
  • Knowledge Base: A basic understanding of drug, device, and biologic development, as well as familiarity with industry guidelines such as ICH-GCP and CDISC standards (CDASH, SDTM, ADaM).

Preferred Skills

While the minimum requirements are essential, candidates with the following attributes will be given preference:

  • Experience in a clinical, scientific, or healthcare discipline.
  • Familiarity with medical coding dictionaries such as MedDRA and WHODrug.
  • Specific experience in oncology and orphan drug therapeutic areas.

Why Join Us?

At Precision for Medicine, we are dedicated to empowering our employees to succeed. We provide comprehensive training and continuous professional development opportunities that foster both personal and career growth. By joining our team, you will be part of an innovative culture that values creativity, collaboration, and commitment to patient care.

What We Offer

  • Competitive salary and benefits package
  • Opportunities for professional development and training
  • A collaborative and inclusive work environment
  • The chance to work on cutting-edge clinical trials and contribute to impactful healthcare solutions

Application Link

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