Fortrea Hiring for B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Life Sciences
| Position | Centralized Study Specialist I |
|---|---|
| Organization | Fortrea |
| Qualification | B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Life Sciences |
| Experience | 3-8 years |
| Location | Bangalore |
| Salary | Not disclosed |
| Key Skills | Project Management, Database Management, Clinical Systems, Problem Solving, Leadership, Communication |
| Walk-in Interview | September 28, 2024, 10:00 AM – 2:00 PM |
| Interview Address | MSR Vaishnavi 29, Union St, Near Cubbon Park Metro Station, Shivaji Nagar, Bengaluru |
Fortrea Hiring: Centralized Study Specialist I (Walk-In Interview)
Are you eager to be part of a global leader in clinical research? Fortrea, a pioneering contract research organization (CRO), is conducting a walk-in interview on September 28, 2024, in Bangalore, for the role of Centralized Study Specialist I. This exciting opportunity allows you to contribute to cutting-edge drug and device development, and make a tangible difference in the healthcare industry.
Why Choose Fortrea?
Fortrea has a reputation for excellence, with over 19,000 employees across the globe. The organization’s mission is to transform the development of drugs and medical devices through innovative clinical research and advanced technology solutions. Working at Fortrea offers the chance to contribute to life-saving therapies that reach patients faster, changing lives for the better.
If you’re someone who is passionate about clinical research, patient safety, and delivering high-quality results, Fortrea is the ideal place for you to build a rewarding career.
Key Responsibilities of a Centralized Study Specialist I
As a Centralized Study Specialist I, you’ll be at the heart of the clinical development process, supporting various aspects of clinical trials. Your role will involve tracking study progress, maintaining clinical systems and databases, and supporting Clinical Research Associates (CRAs) with critical operational activities. Below are the primary responsibilities:
1. Ensure SOP Compliance
You’ll be responsible for following the organization’s Standard Operating Procedures (SOPs) and Work Instructions, ensuring that clinical trial processes are conducted efficiently and in compliance with regulations.
2. Execute Monitoring and Reporting Plans
As a Centralized Study Specialist, you’ll be tasked with executing timely and high-quality monitoring and reporting plans. This involves tracking project metrics and providing updates to management according to strict timelines.
3. Manage Clinical Systems and Databases
Part of your role will involve managing clinical trial systems like CTMS (Clinical Trial Management System), IWRS (Interactive Web Response System), and EDC (Electronic Data Capture) systems. Your job is to ensure that data is entered, tracked, and reported accurately.
4. Assist CRAs and Generate Reports
Supporting Clinical Research Associates (CRAs) will be another key responsibility. You’ll track any outstanding issues, assist in vendor and site payments, and generate study-specific reports for stakeholders.
5. Facilitate Communication and Collaboration
Collaboration is crucial at Fortrea. You’ll work closely with cross-functional teams, including support groups and vendors, to ensure smooth progress on clinical studies. Leading team meetings and managing internal and external communications are part of the role.
Qualifications and Skills Needed
To be successful as a Centralized Study Specialist at Fortrea, you’ll need:
- 3-8 years of experience in a relevant field such as clinical research, with expertise in managing clinical systems and databases.
- A degree in Life Sciences or a related discipline.
- Proven ability to work in a team-oriented environment while delivering projects on time.
- Strong organizational skills and attention to detail, enabling you to track metrics, identify areas for improvement, and ensure project milestones are met.
- Proficiency in project management tools like MS Project and CTMS is a must.
Walk-In Interview Details
Fortrea is hosting a Walk-In Interview on September 28, 2024, from 10:00 AM to 2:00 PM, at MSR Vaishnavi 29, Union St, Near Cubbon Park Metro Station, Shivaji Nagar, Bengaluru, Karnataka. This is a great opportunity to showcase your skills, experience, and passion for clinical research.
Why You Shouldn’t Miss This Opportunity
Working at Fortrea gives you the opportunity to be part of groundbreaking developments in the healthcare industry. With over 20 therapeutic areas covered, you’ll be at the forefront of clinical innovation, helping bring life-changing therapies to patients worldwide. If you have a passion for clinical development, project management, and problem-solving, Fortrea offers an exciting career path that allows you to grow and make an impact.
Don’t miss the chance to join one of the world’s leading CROs—be sure to attend the walk-in interview and start your journey with Fortrea!