Koncord Clinical Research Services (KCRS) is seeking a highly motivated and detail-oriented In-House Clinical Research Coordinator to join our growing team. This is a remote position, ideal for candidates based in Hyderabad, India, offering a unique opportunity to contribute significantly to impactful clinical trials. If you’re a PharmD graduate with a passion for clinical research and a meticulous approach to data management, we encourage you to apply.
About Koncord Clinical Research Services (KCRS)
Koncord Clinical Research Services (KCRS) is a [Insert brief description of KCRS – its mission, size, areas of expertise, etc. E.g., dynamic and rapidly expanding clinical research organization dedicated to advancing medical breakthroughs. We pride ourselves on our commitment to ethical conduct, data integrity, and collaborative partnerships with leading pharmaceutical companies.]. We are committed to providing high-quality clinical research services and fostering a supportive and collaborative work environment for our team members.
A Rewarding Opportunity: Join Our Team!
This is an exciting opportunity to be part of a team making a real difference in the healthcare industry. As an In-House Clinical Research Coordinator, you will play a vital role in ensuring the accuracy, integrity, and timeliness of data within our clinical trials. You will collaborate closely with experienced professionals, contributing to the successful execution of critical research projects. This role offers the flexibility of a remote work environment, combined with the structure and support of a thriving organization.
Key Responsibilities of the In-House Clinical Research Coordinator
This position demands a high level of accuracy, attention to detail, and strong organizational skills. Your core responsibilities will include:
- Data Management & Entry: Manage electronic data entry processes for clinical trials, ensuring accuracy and adherence to strict timelines. This includes inputting and verifying clinical trial data into electronic databases, employing meticulous attention to detail to prevent errors.
- Protocol Development & Adherence: Collaborate with clinical research teams to develop and implement data entry protocols and standards, ensuring compliance with all relevant regulatory requirements and Good Clinical Practice (GCP) guidelines.
- Quality Control & Auditing: Conduct thorough quality checks and audits on data entries, identifying and resolving discrepancies promptly. This involves proactively identifying potential data integrity issues and implementing corrective actions.
- Stakeholder Communication: Maintain effective communication with principal investigators, study coordinators, and other stakeholders to ensure the seamless execution of clinical trials. This includes providing regular updates on data entry progress and addressing any concerns that arise.
- Reporting & Analysis: Generate comprehensive reports and summaries of data entry activities for review by project stakeholders. These reports should clearly communicate key findings and trends within the data.
- Regulatory Compliance: Stay current on all relevant regulations and guidelines concerning electronic data entry in clinical trials, ensuring all work meets the highest standards of compliance.
- Process Improvement: Participate in process improvement initiatives to enhance the efficiency and accuracy of data entry workflows. This includes proposing innovative solutions to optimize data management processes.
- Clinical Trial Coordination: (Depending on the seniority of the role) Coordinate and oversee all aspects of clinical trial activities conducted within the organization. This may involve managing timelines, budgets, and resources for specific projects.
Qualifications
To succeed in this role, you will need the following:
- Education: PharmD degree is required.
- Experience: Prior experience in data entry, preferably within a clinical research setting, is essential. Experience with electronic data capture (EDC) systems is highly desirable.
- Technical Skills: Proficiency in using the Microsoft Office Suite (Word, Excel, PowerPoint) and other relevant software applications is a must. Familiarity with various clinical trial management software packages (e.g., [Mention Specific Software if applicable]) is a significant advantage.
- Soft Skills: Strong attention to detail, excellent organizational skills, and the ability to work both independently and collaboratively within a multidisciplinary team are crucial. Exceptional communication and interpersonal skills are necessary for effective stakeholder interaction.
- Regulatory Knowledge: A solid understanding of Good Clinical Practice (GCP) guidelines and other regulatory requirements for clinical trials is essential.
- Problem-solving abilities: A proactive approach to identifying and addressing challenges in data entry processes is crucial. The ideal candidate will be solution-oriented and able to effectively resolve data integrity issues.
Apply Now
If you meet the qualifications and are eager to embark on a rewarding career in clinical research, please submit your resume and cover letter to: bhanu@koncordclinical.com
