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Insignia Clinical Services Hiring for Clinical Trial Assistant

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Insignia Clinical Services

1 years

Delhi

B pharm, M Pharm, Msc, Bsc, Pharm.D, Lifesciences

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Insignia Clinical Services Private Limited, a leading clinical research organization based in Delhi, is seeking highly motivated and experienced Clinical Trial Assistants (CTAs) to join our growing team. We offer a dynamic work environment, competitive compensation packages, and opportunities for professional growth within the exciting field of clinical trials. This is an excellent opportunity for dedicated professionals to contribute to groundbreaking research and advance their careers in a reputable organization.

About Insignia Clinical Services:

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Insignia Clinical Services is a rapidly expanding clinical research organization committed to delivering high-quality clinical trial services to pharmaceutical and biotechnology companies. We pride ourselves on our unwavering commitment to ethical conduct, scientific rigor, and patient well-being. Our team of experts brings extensive knowledge and experience to every project, ensuring the highest standards of excellence are maintained throughout the clinical trial process. We foster a collaborative and supportive environment where innovation and professional development are encouraged.

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Job Description: Clinical Trial Assistant (CTA)

We are currently seeking four highly skilled and dedicated Clinical Trial Assistants to join our team in Delhi. As a CTA at Insignia, you will play a crucial role in supporting the successful execution of clinical trials. Your responsibilities will encompass a wide range of tasks, providing invaluable support to the clinical research team. This is a fantastic opportunity to gain practical experience, contribute meaningfully to medical advancements, and build a rewarding career in the dynamic world of clinical research.

Key Responsibilities:

  • Study Startup Activities: Participate in the initiation and planning phases of clinical trials, including protocol review, regulatory document preparation, and site selection activities.
  • Patient Recruitment and Screening: Assist in the recruitment and screening of potential study participants, ensuring compliance with all relevant guidelines and regulations.
  • Data Management: Contribute to the accurate and timely collection, entry, and management of clinical trial data. This includes meticulous record-keeping and adherence to data quality standards.
  • Regulatory Compliance: Support the clinical research team in maintaining compliance with Good Clinical Practice (GCP) guidelines, regulatory requirements, and internal procedures.
  • Logistics and Coordination: Assist in coordinating logistics for clinical trial activities, including scheduling appointments, managing supplies, and liaising with various stakeholders.
  • Reporting and Documentation: Participate in the preparation of progress reports, regulatory submissions, and other essential documentation.
  • Maintaining Patient Confidentiality: Adhere strictly to all patient confidentiality guidelines and regulations.

Qualifications and Experience:

To be successful in this role, you should possess the following qualifications and experience:

  • Educational Background: A Master’s degree in Life Sciences (e.g., Biology, Pharmacology, Biotechnology) or a relevant scientific field, or a Bachelor of Pharmacy (B. Pharm) is required.
  • Professional Experience: A minimum of one year of experience working as a Clinical Trial professional is essential. Experience with various aspects of clinical trial management, including data management, regulatory compliance, and patient recruitment, will be highly advantageous.
  • Technical Skills: Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) is required. Experience with electronic data capture (EDC) systems is highly desirable.
  • Soft Skills: Strong organizational and time-management skills are crucial. Excellent communication, interpersonal, and teamwork abilities are essential. Attention to detail and commitment to accuracy are paramount in this role.

Compensation and Benefits:

Insignia Clinical Services offers a highly competitive compensation and benefits package that reflects industry standards. We are committed to providing a rewarding and supportive work environment that fosters professional growth and development. Specific details regarding compensation will be discussed during the interview process.

How to Apply:

Interested and qualified candidates are encouraged to submit their CV and cover letter to: careers@insigniacs.com. Please include a compelling summary of your experience and qualifications in your cover letter, highlighting your relevant skills and achievements.

Learn More:

For more information about Insignia Clinical Services and our commitment to excellence in clinical research, please visit our website: www.insigniacs.com or connect with us on LinkedIn: https://www.linkedin.com/in/insignia-clinical-services

Insignia Clinical Services Hiring for Clinical Trial Assistant

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