Work From Home Clinical Research Associate at ICON Plc
Looking to take your career in clinical research to the next level? ICON Plc, the world’s largest and most comprehensive clinical research organization, is hiring a Clinical Research Associate. This is a work-from-home position that allows you to contribute to life-saving clinical trials from the comfort of your home while collaborating with global teams. ICON Plc offers an inclusive and dynamic work environment that values diversity, innovation, and continuous improvement. Work From Home Clinical Research Associate at ICON Plc
Here’s what you need to know about the role:
Key Details at a Glance
Position | Clinical Research Associate |
---|---|
Company | ICON Plc |
Location | Work From Home |
Experience | 1 to 2 Years |
Qualification | B.Pharm, M.Pharm, Pharm D, BDS, MBBS |
Salary | 4 – 6 Lacs Per Year |
Job Posted on | October 5, 2024 |
Remote Work | Eligible |
Why Choose ICON Plc?
ICON Plc is a leading clinical research organization that drives healthcare innovation by conducting cutting-edge clinical trials globally. As a Clinical Research Associate, you will have the chance to work in an environment where your contributions directly impact patient lives. Whether you’re looking for flexibility, career growth, or the opportunity to work with a diverse team of professionals, ICON Plc provides an ideal work environment for motivated individuals. Work From Home Clinical Research Associate at ICON Plc
What You’ll Do as a Clinical Research Associate
As a Clinical Research Associate at ICON Plc, you will be responsible for ensuring the smooth execution of clinical trials at designated sites. This includes monitoring and ensuring that all clinical research activities comply with industry standards and study protocols. Some of your key responsibilities will include:
1. On-Site Monitoring Work From Home Clinical Research Associate at ICON Plc
Your primary role will involve conducting on-site monitoring of clinical trials. This is crucial to ensure that trials are conducted in compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
2. Institutional Review Board (IRB) Submissions
You will be responsible for preparing and submitting the necessary documentation to the Institutional Review Board (IRB), ensuring all approvals are obtained before trial initiation.
3. Managing Study Sites Work From Home Clinical Research Associate at ICON Plc
You’ll manage the responsible sites throughout the study lifecycle, from initiation to close-out, ensuring they meet the study’s objectives and compliance standards.
4. Communication with Site Staff Work From Home Clinical Research Associate at ICON Plc
Regular communication with site staff is essential. You will ensure that all staff members are aware of their responsibilities and that they follow study protocols meticulously.
5. Collaboration with Stakeholders Work From Home Clinical Research Associate at ICON Plc
Collaborating with various stakeholders, including vendors, sponsors, and regulatory authorities, you’ll work to ensure that trials are conducted successfully, and all challenges are effectively addressed.
Qualifications and Experience Required
To excel in this role, candidates must meet the following eligibility criteria:
- Education: A Bachelor’s or Master’s degree in relevant fields, such as B.Pharm, M.Pharm, Pharm D, BDS, or MBBS, from an accredited institution.
- Experience: A minimum of 1-2 years of onsite monitoring experience, particularly in Oncology. Please note that any training or induction period will not count towards this experience.
- Skills: Strong communication skills are critical. You’ll need to effectively communicate with site staff, vendors, and stakeholders to ensure trials run smoothly.
Why This Role Stands Out
- Work From Home Flexibility: Enjoy the benefit of working remotely, allowing you to balance professional and personal commitments while contributing to impactful clinical research.
- Competitive Salary: With a salary range of 4 to 6 Lacs per year, this position offers a competitive package for professionals with the right experience.
- Global Exposure: By joining ICON Plc, you’ll work alongside industry leaders and gain exposure to global clinical trials, adding tremendous value to your career trajectory.
How to Apply
If you’re excited about this opportunity and meet the required qualifications, apply through the designated portal or get in touch with Sonia Oh for more information on the application process. This is your chance to join a company that values innovation and excellence in clinical research.
Applucation Link
Final Thoughts
Becoming a Clinical Research Associate at ICON Plc is an exciting opportunity for professionals looking to advance their careers in clinical research. With the chance to work from home, a competitive salary, and the opportunity to be part of a global clinical trial team, this position offers the perfect blend of flexibility, challenge, and growth. If you have experience in oncology clinical trials and a passion for improving healthcare outcomes, this could be the perfect role for you. Apply today and become part of a team that is making a real difference in the world!