Are you passionate about advancing clinical research? Koncord Clinical Research Services is thrilled to announce that applications are now open for the In-House Clinical Research Coordinator position in Hyderabad! This is your chance to join a dynamic team dedicated to excellence in clinical trials. If you’re a Pharm D graduate with at least 6 months of experience in clinical research, seize this opportunity to make a difference in healthcare innovation. Apply today and become part of our mission to drive cutting-edge clinical research!
Key Responsibilities
As an In-House Clinical Research Coordinator at Koncord, you will play a pivotal role in ensuring the success of clinical trials. Your responsibilities will include:
- Managing Data Entry: Oversee electronic data entry for clinical trials, ensuring accuracy and timeliness.
- Collaborating with Teams: Work closely with clinical research teams to establish data entry protocols and standards.
- Data Verification: Input and verify clinical trial data into electronic databases with precision.
- Quality Assurance: Conduct regular quality checks and audits to ensure compliance with regulatory standards.
- Stakeholder Coordination: Liaise with principal investigators, study coordinators, and other stakeholders for seamless trial execution.
- Maintaining Data Integrity: Ensure confidentiality and integrity of clinical trial data.
- Reporting: Generate detailed reports and summaries of data entry activities for stakeholders.
- Study Participation: Attend study meetings, site visits, and audits as required.
- Regulatory Compliance: Stay updated on Good Clinical Practice (GCP) guidelines and clinical trial regulations.
- Process Improvement: Contribute to initiatives that enhance data entry efficiency and accuracy.
- Trial Oversight: Coordinate and manage all aspects of in-house clinical trial activities.
Qualifications
To excel in this role, candidates must meet the following criteria:
- Education: Bachelor’s degree in Life Sciences, Pharmacy, or Pharm D.
- Experience: Minimum 6 months of work experience in clinical research or data entry.
- Technical Skills: Familiarity with electronic data capture (EDC) systems and clinical trial management software.
- Attention to Detail: Strong organizational skills and meticulous attention to detail.
- Teamwork: Ability to work independently and collaboratively in a multidisciplinary team.
- Communication: Excellent interpersonal and communication skills.
- Software Proficiency: Expertise in Microsoft Office Suite and relevant software applications.
- Regulatory Knowledge: Understanding of GCP guidelines and clinical trial regulations.
- Problem-Solving: Proactive approach to addressing challenges in data entry processes.
- Location: Must be based in Hyderabad.
Benefits of Joining Koncord
- Career Growth: Work with a leading clinical research organization and gain hands-on experience in cutting-edge trials.
- Collaborative Environment: Join a passionate, multidisciplinary team dedicated to healthcare innovation.
- Professional Development: Access opportunities to stay updated on industry regulations and best practices.
- Impactful Work: Contribute to clinical trials that advance medical research and improve patient outcomes.
How to Apply
eady to take the next step in your clinical research career? Send your updated CV to hr@koncordclinical.com with the subject line “In-House Clinical Research Coordinator Application – [Your Name].”
