Clinical Data Associate II Vacancy | Trialmed PPD Clinical Research Bangalore

Clinical Data Associate II Vacancy | Trialmed PPD Clinical Research Bangalore

Apply for Clinical Data Associate II at Trialmed (PPD, Thermo Fisher Scientific), Bangalore. Openings for graduates with 2+ years’ data management experience.

---

Trialmed, a global site network and the early phase clinical solution for PPD® clinical research, part of Thermo Fisher Scientific Inc., is hiring for the role of Clinical Data Associate II (CDA) in Bangalore, India. This fully remote role provides an exceptional opportunity to join a leading global contract research organization (CRO) dedicated to accelerating drug development and bringing cures to market.

Company Overview

Thermo Fisher Scientific is a world leader in serving science, with the mission to make the world healthier, cleaner, and safer. Through its PPD clinical research division, Thermo Fisher advances clinical trial data management and operations on a global scale. Trialmed, as part of PPD, powers early phase clinical research with cutting-edge data-driven solutions. Joining this team means contributing directly to innovative drug development and patient health worldwide.

Job Role & Responsibilities

As a Clinical Data Associate II, you will be responsible for managing critical aspects of clinical trial data, ensuring accuracy, compliance, and regulatory alignment. Your responsibilities include:

• Identifying and resolving data discrepancies and updating clinical databases.
• Generating, tracking, and resolving data clarifications and queries.
• Reviewing data listings for accuracy, consistency, and regulatory compliance.
• Producing regular status reports for CDM management and sponsors.
• Managing Serious Adverse Event (SAE) and Third-Party Vendor data reconciliations.
• Performing advanced data cleaning processes to ensure patient safety and efficacy analysis.
• Working independently on complex assignments requiring critical thinking and innovation.
• Contributing to CRF (Case Report Form) design and database development.
• Facilitating effective communication with internal teams, sponsors, and global partners.

Eligibility / Qualifications

• Education: Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Clinical Research, or related fields.
• Experience:
  • Minimum 2+ years of data management or related experience.
  • Hands-on expertise with clinical trial data management tools.
• Skills:
  • Proficiency with Medidata Rave, Veeva Vault, and EDC databases.
  • Strong knowledge of GCP, eTMF, and data validation processes.
  • Excellent written and verbal communication in English.
  • Strong analytical, problem-solving, and documentation skills.
  • Ability to manage projects independently with minimal supervision.
  • Adaptability to global teams, diverse cultures, and dynamic environments.

Location & Salary

• Job Location: Bangalore, Karnataka, India (remote opportunity).
• Work Mode: Fully remote / Hybrid / Office (flexible).
• Work Schedule: 1:00 PM to 10:00 PM IST (Second Shift).
• Salary: Competitive, based on experience and qualifications.

Application Process

Candidates interested in joining the global PPD/Trialmed team can apply through the official Thermo Fisher Scientific careers portal: Apply Here

Apply early to maximize your chance of being shortlisted!

---

FAQs

1. Who is eligible to apply?
Graduates in Life Sciences, Pharmacy, Biotechnology, or related fields with at least 2 years’ data management experience.

2. Is prior experience with EDC tools required?
Yes, experience with Medidata Rave, Veeva Vault, or similar EDC systems is preferred.

3. Can this role be performed remotely?
Yes, this position offers remote, hybrid, and office work options.

4. What is the standard work schedule?
The role requires working second shift hours (1:00 PM – 10:00 PM IST).

5. What is the career growth potential?
Clinical Data Associates at Trialmed gain exposure to global projects, cutting-edge data technologies, and career progression in clinical data management.

---

Career Benefits at Trialmed (PPD/Thermo Fisher Scientific)

• Be part of a leading global CRO shaping the future of clinical research.
• Exposure to international data management standards and regulatory compliance.
• Career growth in clinical trials, data management, and biostatistics.
• Flexibility to work remotely, enabling better work-life balance.
• Access to training, global networking, and advanced digital tools.

---

Summary Table

Company	Trialmed (PPD, Thermo Fisher Scientific)
Vacancies	Not specified
Required Education	B.Sc, M.Sc, B.Pharm, M.Pharm, Biotechnology, Life Sciences, Clinical Research
Experience	2+ years in Clinical Data Management
Location	Bangalore, Karnataka, India (Remote/Hybrid/On-site)