Clinical Research Associate at Omega Healthcare
| Position | Clinical Research Associate |
|---|---|
| Organization | Omega Healthcare |
| Qualification | B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Life Sciences |
| Experience | 6 Months – 1 Year |
| Location | Mumbai |
| Salary | Not Disclosed |
| Key Skills | Knowledge of Oncology Terminology, EDC Systems, Protocol Monitoring, GCP Compliance, Multitasking |
Join Omega Healthcare: Exciting Opportunity for Clinical Research Associates
Are you looking to build a rewarding career in clinical research? Omega Healthcare, a leader in healthcare management services, is actively hiring for the role of Clinical Research Associate (CRA) in Mumbai. If you have experience in managing clinical trials, a passion for ensuring patient safety, and a desire to work in a fast-paced environment, this is the perfect opportunity for you! Clinical Research Associate at Omega Healthcare
Why Omega Healthcare?
Omega Healthcare is at the forefront of healthcare outsourcing and management services. Their work spans across a variety of sectors including clinical research, patient care, and health data management. They are known for their commitment to quality and ensuring the highest standards of compliance and operational efficiency. By joining Omega Healthcare, you’ll be part of a team that values integrity, patient safety, and innovation in every project.
Key Responsibilities of a Clinical Research Associate
As a Clinical Research Associate (CRA) at Omega Healthcare, you’ll play a crucial role in ensuring the success of clinical trials. Your work will directly impact the advancement of medical research, and you’ll be responsible for managing critical aspects of the trial process.
Here are some of the key responsibilities you’ll handle:
1. Project & Operations Management
From initiating trials to closing them, you’ll be responsible for managing all operational aspects. This includes preparing and maintaining trial documentation, coordinating with investigators, and submitting findings to sponsors. A high degree of attention to detail will be required to ensure that trials are conducted efficiently and in compliance with all guidelines.
2. Quality Assurance
A core part of your job will be to ensure that clinical trials adhere to ICH-GCP guidelines (International Conference on Harmonization – Good Clinical Practice). You will work to enhance the consistency and quality of Electronic Data Capture (EDC) systems used during trials, ensuring that data is recorded and stored accurately.
Your ability to spot inconsistencies and ensure quality data will be vital in maintaining the integrity of clinical research.
3. Protocol Monitoring
Monitoring the trial’s progress and ensuring that investigators follow Good Clinical Practice (GCP) is a critical aspect of this role. You’ll be responsible for ensuring that trial protocols are strictly followed, and any deviations or concerns must be communicated to sponsors quickly. Your ability to keep trials on track while ensuring compliance with all protocols is key to the success of these research efforts.
4. Security Responsibilities
The importance of data security in clinical research cannot be overstated. As a CRA, you’ll need to ensure that all trial data remains confidential and that patient privacy is maintained at all times. You’ll follow strict data security protocols to avoid any breaches or mishandling of sensitive information.
Requirements to Succeed as a Clinical Research Associate
To thrive in this role at Omega Healthcare, you’ll need the following qualifications and skills:
- Educational Background: A Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or Clinical Research is essential.
- Experience: At least 6 months to 1 year of experience in clinical trials management is required. Candidates with certification in clinical research are highly preferred.
- Technical Skills: Proficiency with Electronic Data Capture (EDC) systems such as Medidata RAVE, Oracle, or Inform is a major advantage.
- Knowledge of Oncology Terminology: While not mandatory, experience with oncology-specific terminology will be a bonus, especially in specialized trials.
- Multitasking Abilities: Strong organizational skills and the ability to juggle multiple tasks and responsibilities are key.
- Communication Skills: Excellent written and verbal communication is necessary, as you will be interacting with both internal teams and external sponsors.
How to Apply
If you’re excited to join a leading healthcare organization like Omega Healthcare, don’t miss out on this opportunity! To apply, send your resume to Krushikant Pawar at krushikantpawar@gmail.com, or reach out via phone at 7892374090.
Why You Shouldn’t Miss This Opportunity
Becoming a Clinical Research Associate at Omega Healthcare means working in a fast-growing industry where you can make a real impact on healthcare and medical research. Not only will you be involved in advancing cutting-edge medical solutions, but you’ll also be part of a team that is dedicated to improving patient safety and data integrity. If you’re passionate about clinical trials and have the skills and drive to succeed, Omega Healthcare is the place for you!
Apply today, and take the next big step in your clinical research career!