Job at Precision For Medicine – Apply Now For Study Design Lead
Precision For Medicine invites applications for a high-impact job at Precision For Medicine as a Study Design Lead in Bengaluru, offering a challenging documentation job role in clinical trial design and laboratory services. This role provides a unique opportunity to work at the forefront of clinical trial design, laboratory services, and translational research. Candidates will gain hands-on experience in technical writing for clinical research, project coordination in the life sciences, and contribute to innovative healthcare solutions.
- Position Title: Study Design Lead
- Location: Bengaluru, Karnataka, India
- Department: Clinical Operations & Laboratory Services
About The Company
Precision For Medicine is a globally recognized leader in clinical trial design and laboratory services, dedicated to advancing personalized medicine. The company delivers innovative solutions in biomarker discovery, translational research, and project management to accelerate drug development and improve patient outcomes. With a culture of collaboration and excellence, Precision For Medicine empowers its teams to deliver meaningful impact in the biotechnology and life sciences sectors.
Position Overview
Support role that works with internal teams to review, update, and assist with the completion of study startup documents with oversight from a Study Design Lead. Assists with administrative tasks.
Key Responsibilities
The selected Study Design Lead will:
- Collaborate with internal teams to review, update, and complete study startup documents and project specification documentation.
- Assist in the development of Lab Manuals, Kit Design documents, Sample Management processes, and Project Operating Procedures.
- Ensure all study design deliverables meet regulatory standards, quality benchmarks, and client expectations.
- Support coordination across Project Management, Clinical, and Laboratory teams to ensure smooth execution of studies.
- Manage and maintain study-related documents, ensuring compliance and accuracy — a critical aspect of this documentation job in clinical research.
- Assist in preparing reports, regulatory documentation, and supporting materials for submission.
- Manage priorities to meet deadlines and deliverables with high quality.
Eligibility Criteria
Minimum Qualifications:
- Bachelor’s degree in Life Sciences, Biotechnology, Engineering, or a related field.
Additional Skills and Requirements:
- Excellent technical writing and documentation skills in clinical research.
- Strong understanding of clinical trial design, laboratory processes, and study operations.
- Proficiency with MS Office/MS 365 applications.
- Exceptional organizational, communication, and multi-tasking abilities.
- Analytical thinking, problem-solving skills, and attention to detail.
- Ability to work extended hours if required to meet project deadlines.
- Fluency in English (written and spoken).
Key Skills and Competencies
- Clinical trial design expertise
- Project coordination in life sciences
- Technical writing in clinical research
- Regulatory documentation management
- Laboratory services workflow understanding
- Team collaboration and stakeholder engagement
- Critical thinking and data analysis
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Strong skills in clinical trial documentation and management to excel in this documentation job.
Why Join Precision For Medicine
- Gain hands-on exposure to cutting-edge clinical trial design and laboratory services.
- Work in a globally respected organization, driving innovation in personalized medicine.
- Collaborate with multidisciplinary teams on impactful healthcare projects.
- Enhance career growth with exposure to regulatory environments and advanced research methodologies.
- Be part of a culture that encourages innovation, collaboration, and scientific excellence.
