PSI CRO AG Hiring for Study Startup Associate (Clinical Research)
| Position | Study Startup Associate (Clinical Research) |
|---|---|
| Company | PSI CRO AG |
| Location | Bangalore |
| Experience | 1 to 2 Years |
| Salary Range | ₹25,000 – ₹35,000/month |
| Start Date | September 28, 2024 |
| Education Requirement | MD, PharmD, RN, or Life Sciences Degree |
| Skills Needed | Communication, Time Management, Flexibility, Problem Solving |
| Key Responsibilities | Site startup timelines, document submissions, regulatory approvals, budget negotiations, tracking |
Join PSI CRO AG as a Study Startup Associate in Clinical Research
Are you passionate about advancing medical science while growing your career in clinical research? PSI CRO AG, a globally recognized Clinical Research Organization (CRO), offers you the chance to make a difference in patients’ lives by helping bring new treatments to the market. We are looking for a Study Startup Associate in our Bangalore office, where you’ll contribute to the seamless execution of clinical trials and play a key role in bringing life-changing medicines to patients.
Who is PSI CRO AG?
PSI CRO AG, founded in 1995, has grown to become one of the world’s top clinical research organizations, known for its dedication to both medical science and its employees. With over 2,700 employees worldwide, PSI fosters an environment where people and excellence come first. Based in Switzerland, PSI operates globally, delivering high-quality clinical trials with personalized care and attention. The company consistently ranks as one of the top CROs for its client-focused approach and its mission to improve global health.
Why Should You Join Us?
PSI is not just another organization; it’s a place where you can thrive professionally and personally. If you are looking to work with passionate experts dedicated to making a tangible difference in healthcare, this is the right fit for you. At PSI, we value our employees’ growth as much as our mission to advance clinical research. Our work culture encourages flexibility, problem-solving, and excellent time management—all while helping you hone your skills and career.
What Will You Be Doing?
As a Study Startup Associate in Bangalore, you’ll be pivotal in getting clinical trials off the ground, making sure every project runs on schedule. You’ll manage site-specific startup timelines, ensuring that all ethics and regulatory approvals are handled efficiently.
Key responsibilities include:
- Site-Specific Timelines: Develop and manage startup schedules to hit site activation targets, ensuring timely execution of clinical trials.
- Document Review & Submission: You’ll handle the collection, review, and submission of critical documents to ethics boards and regulatory authorities, ensuring nothing falls through the cracks.
- Budget & Contract Negotiations: You’ll be at the forefront of negotiating budgets and contracts with clinical sites, helping smooth out the process for all stakeholders.
- Tracking Systems: It’s vital to keep everything organized. You’ll maintain tracking and filing systems that ensure the startup processes are efficient and well-documented.
- Drug Release: Preparing site document packages is key to ensuring the release of drugs for clinical trials.
What Are We Looking For?
To qualify for this exciting role, you’ll need an MD, PharmD, RN, or a university degree in life sciences, or an equivalent blend of education and hands-on experience in clinical trial processes. Experience with Indian clinical sites, especially in startup processes, is critical. You should also have strong English proficiency, as clear communication is essential to your success.
Ideal skills include:
- Regulatory Submission Expertise: You’ll be handling submissions for ethics and regulatory approvals, so familiarity with this process is key.
- Time Management & Organization: You’ll be creating and maintaining timelines and tracking systems for each project.
- Excellent Communication: The ability to foster relationships and manage negotiations across all levels of the organization is critical.
- Proactive Attitude: PSI values problem solvers who are detail-oriented and can anticipate issues before they arise.
A Career That Makes a Difference
Working at PSI CRO AG is more than just a job—it’s a career in making a global impact. Every project you touch will play a role in developing new treatments, ultimately improving the health and lives of people around the world. If you’re looking for a role that combines challenge, impact, and professional growth, PSI CRO AG is the perfect place to start.
Apply now to begin your journey in clinical research with a company that values both its people and its mission.