Project Support Coordinator

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πŸ›‘οΈ Verified Career Listing Directly reviewed and cross-referenced with hiring sources.

Thermo Fisher Scientific

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πŸŽ“ Research
πŸ“ Banglore
πŸ’Ό Fresher
βœ” Verified Job
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The Project Support Coordinator will coordinate and oversee assigned clinical trial activities while ensuring tasks are completed on time, within budget, and to required quality standards. The role involves supporting study documentation, clinical trial systems, project trackers, file reviews, and administrative activities. The successful candidate will work closely with clinical teams, internal stakeholders, vendors, investigators, and clients to maintain study readiness and ensure timely resolution of issues. Experience or exposure to systems such as CTMS, Oracle Activate, and eTMF will be valuable. This opportunity offers a strong platform to develop expertise in clinical research operations and project coordination within a global life sciences organization.

Job Overview

Particulars Details
Position Project Support Coordinator
Company Thermo Fisher Scientific
Location Banglore
Job Type Full-Time
Experience Fresher
Category / Department Research
Application Mode Email

🏒 About Thermo Fisher Scientific

Thermo Fisher Scientific Inc. is a global leader in serving science, with annual revenue of more than $40 billion. The company supports customers across life sciences research, analytical challenges, laboratory productivity, diagnostics, and the development and manufacturing of life-changing therapies.

Company Mission
The company’s mission is to enable customers to make the world healthier, cleaner, and safer by providing innovative technologies, services, and solutions that support scientific progress.

Company Vision
Thermo Fisher Scientific strives to advance science and improve human health by helping researchers, healthcare professionals, laboratories, and organizations solve complex scientific and healthcare challenges.

Core Values

πŸ”Ή Innovation and scientific excellence
πŸ”Ή Customer-focused problem solving
πŸ”Ή Integrity and accountability
πŸ”Ή Collaboration and teamwork
πŸ”Ή Commitment to quality
πŸ”Ή Purpose-driven work
πŸ”Ή Continuous learning and development

What Makes Them Different
Thermo Fisher Scientific brings together scientific technologies, laboratory solutions, diagnostics capabilities, and pharmaceutical services under a global organization. Its broad portfolio supports customers throughout the scientific and healthcare ecosystem, from accelerating research to developing therapies and improving patient health.

Leadership / Company Philosophy
The company emphasizes innovation, purpose, and collaboration. Its global workforce is encouraged to develop critical solutions that address important scientific and healthcare challenges while building meaningful and rewarding careers.

The organization operates through leading brands including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.

πŸ“
Office Location

πŸ“ Location: Bangalore, Karnataka, India

πŸ’‘ Editor's Note / Preparation Tip

πŸ“„ Resume Preparation Tips

1️⃣ Highlight experience in clinical research, clinical trials, project coordination, or life sciences operations.
2️⃣ Mention hands-on experience with CTMS, eTMF, Oracle Activate, or other clinical trial systems if applicable.
3️⃣ Showcase your ability to manage trackers, documentation, reports, meeting minutes, and action items.
4️⃣ Include examples demonstrating attention to detail, timely task completion, issue resolution, and stakeholder coordination.
5️⃣ Use measurable achievements wherever possible, such as the number of studies supported, documents managed, or process improvements implemented.

🎯 Interview Preparation

1️⃣ Revise the fundamentals of clinical trials and clinical research operations.
2️⃣ Understand the purpose of TMF/eTMF, ISF, CTMS, study trackers, and clinical trial documentation.
3️⃣ Prepare examples of how you managed multiple priorities and ensured tasks were completed within deadlines.
4️⃣ Be ready to explain how you identify, document, escalate, and follow up on compliance or documentation issues.
5️⃣ Prepare real examples that demonstrate your communication and collaboration skills with internal teams, vendors, clients, or other stakeholders.

πŸ’‘ Professional Tips

1️⃣ Understand the difference between TMF and ISF and their importance in clinical trial documentation.
2️⃣ Learn the basics of audit readiness and inspection preparedness.
3️⃣ Develop strong Excel and reporting skills for managing trackers, metrics, and reconciliation activities.
4️⃣ Improve your understanding of clinical trial lifecycle activities and study start-up processes.
5️⃣ Demonstrate that you are proactive, detail-oriented, organized, and comfortable working with global stakeholders and multiple deadlines.

πŸ“ Job Description

πŸš€ Project Support Coordinator | Thermo Fisher Scientific

🌟 Exciting Career Opportunity in Clinical Research & Project Support!

Thermo Fisher Scientific is looking for a detail-oriented and organized Project Support Coordinator to join its team in Bangalore, India. This role is ideal for professionals interested in clinical trial operations, project coordination, study documentation, systems support, and cross-functional collaboration. If you have strong organizational skills and up to 4 years of relevant experience, this could be a great opportunity to grow your career in the global life sciences industry! πŸ§ͺ🌍


Position Details

Position: Project Support Coordinator
Company: Thermo Fisher Scientific
Location: Bangalore, India
Work Mode: Fully Onsite
Job Type: Full Time
Experience: 0–4 Years of relevant experience
Education: High School / Secondary School Diploma or equivalent with relevant formal academic or vocational qualification
Job Requisition ID: R-01358145
Work Schedule: Other
Environmental Conditions: Office
Posted: Today

Preferred Skills

⭐ Exposure to Clinical Trial Management Systems (CTMS)
⭐ Familiarity with Oracle Activate
⭐ Knowledge of electronic Trial Master Files (eTMF)
⭐ Experience with Investigator Site Files (ISF)
⭐ Understanding of clinical trial project metrics and reporting
⭐ Exposure to vendor management trackers
⭐ Experience supporting meetings, minutes, and action-item tracking
⭐ Familiarity with audit readiness and compliance activities
⭐ Experience in clinical research or pharmaceutical/life sciences environments

Candidate Requirements

πŸŽ“ High School / Secondary School Diploma or equivalent
πŸŽ“ Relevant formal academic or vocational qualification
πŸ“œ Technical positions may require an applicable certificate
πŸ’Ό Previous experience providing relevant knowledge, skills, and abilities comparable to 0–4 years
πŸ§ͺ Interest or experience in clinical research, clinical trials, life sciences, or project coordination is beneficial
πŸ“‹ Strong documentation and organizational abilities
🀝 Ability to collaborate with internal teams, clients, vendors, and clinical stakeholders
πŸ’» Comfortable working with project systems, trackers, and documentation platforms
πŸ“ Willingness to work Fully Onsite in Bangalore

Why Join Thermo Fisher Scientific?

🌍 Become part of a global organization serving the science and healthcare industries
πŸ§ͺ Contribute to work that supports life sciences research and clinical development
πŸš€ Build experience in clinical trial operations and project coordination
πŸ’» Gain exposure to clinical systems, documentation platforms, and project tracking tools
🀝 Collaborate with global teams and diverse stakeholders
πŸ“š Develop valuable skills in study management, documentation, compliance, and operational coordination
🌱 Grow your career within a company focused on innovation and scientific advancement
❀️ Contribute to a mission focused on making the world healthier, cleaner, and safer

How to Apply

πŸ“© Interested candidates can apply through the official Thermo Fisher Scientific careers portal.

πŸ”Ž Job Requisition ID: R-01358145
πŸ“ Location: Bangalore, India
🏒 Work Mode: Fully Onsite

Know someone who would be a great fit? Tag them or share this opportunity with your network! πŸš€


🎯 Key Responsibilities

  • βœ“ Coordinate, oversee, and complete assigned clinical trial activities according to the applicable task matrix.
  • βœ“ Perform department, internal, country, and investigator file reviews as assigned and document identified findings.
  • βœ“ Follow up on findings, support resolution, and escalate critical issues when necessary.
  • βœ“ Ensure allocated activities are completed on time, within budget, and according to required quality standards.
  • βœ“ Monitor task workload and identify significant variances, including overburn or underburn, for self and junior Project Support Coordinators.
  • βœ“ Review and redistribute tasks based on available capacity within the junior PSC team.
  • βœ“ Support the maintenance and oversight of study-specific documentation and global project systems, tools, and trackers.
  • βœ“ Maintain study team lists and track project-specific training requirements.
  • βœ“ Support system access management for organizational teams, vendors, and clients.
  • βœ“ Track project-level activity plans in the appropriate systems.
  • βœ“ Provide support for CTMS, Oracle Activate, and eTMFsystems, including access requests and study-level document management.
  • βœ“ Help maintain audit readiness and communicate non-compliance issues to study teams while supporting resolution planning.
  • βœ“ Process documents sent to CRG or client eTMF systems in a timely manner.
  • βœ“ Conduct CRG/client eTMF reviews and coordinate or propose appropriate issue resolutions.
  • βœ“ Support mass mailings and project-related communications when required.
  • βœ“ Prepare and provide documents and reports to internal team members.
  • βœ“ Support scheduling and organization of client and internal meetings.
  • βœ“ Prepare and distribute meeting minutes and follow up on action items to ensure closure.
  • βœ“ Export and reconcile study metrics reports and, when involved in a Lead role, analyze reports and identify potential issues.
  • βœ“ Maintain and regularly review vendor trackers for accuracy and completeness.
  • βœ“ Coordinate the compilation of Investigator Site File (ISF) templates and pharmacy binders under the guidance of the Clinical Team Manager.
  • βœ“ Attend Kick-off and Project Launch meetings, take notes when required, and support initial study setup activities.

πŸ’‘ Required Qualifications & Skills

βœ“ ️ Strong organizational and coordination skills βœ“ ️ Ability to manage multiple assigned trial activities βœ“ ️ Good attention to detail and documentation accuracy βœ“ ️ Ability to complete tasks within timelines and quality standards βœ“ ️ Understanding of clinical trial documentation and processes βœ“ ️ Ability to review files and document findings βœ“ ️ Strong follow-up and issue-resolution skills βœ“ ️ Ability to maintain trackers and project documentation βœ“ ️ Good communication and collaboration skills βœ“ ️ Ability to work effectively in a fully onsite environment βœ“ ️ Knowledge of administrative and project coordination activities

πŸš€ Career Guidance & Interview Insights

To help you succeed, we've compiled original preparation guides, resume keywords, and growth analytics for this category of role.

Working as a Project Support Coordinator gives you an operational bird's-eye view of the organization. You will streamline processes, coordinate resource allocation, eliminate administrative bottlenecks, and ensure smooth day-to-day business execution. This role builds exceptional leadership, organization, and problem-solving skills.

Expected Career Progression Roadmap:

Operations careers focus on coordination and organization. Progression moves from Administrative Coordinator or Operations Associate to Office Manager or Operations Specialist. Experienced leaders advance to Operations Manager, Director of Operations, and strategic executive leadership such as Chief Operating Officer (COO).

Expected Technical & Behavioral Questions:

  • Q1: How do you prioritize tasks when multiple departments request administrative support simultaneously?
    Answer Tip: Explain categorizing tasks by urgency and impact, setting clear expectations, and utilizing shared ticketing or task boards.
  • Q2: Tell us about a time you optimized an inefficient office process.
    Answer Tip: Discuss identifying paper-heavy delays, digitizing approvals, saving company hours, and obtaining positive team feedback.
  • Q3: How do you manage vendor relationships and negotiate contracts?
    Answer Tip: Talk about conducting multi-vendor bidding, validating service level agreements (SLAs), building long-term goodwill, and regular performance audits.
πŸ’‘ Pro-Tip: Before your interview, research the company's recent news, product launches, and Glassdoor work reviews. Prepare 2-3 thoughtful questions for the interviewer regarding team dynamics and success metrics for this role.

To pass automated ATS (Applicant Tracking System) screening and catch the recruiter's eye, tailor your resume with the following tips:

  • Keywords to include: Vendor Management, Facility Operations, Inventory Control, Process Optimization, Scheduling, Resource Allocation, Procurement, SLA management.
  • Format: Structure your experience chronologically, starting with your operational achievements and process improvements.
  • Quantify Results: E.g., 'Negotiated vendor contracts, reducing corporate facility expenses by 12% without reducing service frequency.'
Estimated Market Compensation in India:

Estimated compensation for this role type in India is β‚Ή2,20,000 - β‚Ή3,60,000 per annum. The actual salary package offered depends on factors such as company size, work mode (remote or on-site), individual technical proficiency, and negotiations during final HR rounds.

Suggested Professional Certifications:

To boost your professional profile, look into: Project Management Professional (PMP), CAPM from PMI, Certified ScrumMaster (CSM), or advanced business communications and spreadsheet management credentials.

Frequently Asked Questions

1️⃣ Where is the Project Support Coordinator role located?
The position is based in Bangalore, India.

2️⃣ Is this a remote or hybrid position?
No. The role is listed as Fully Onsite.

3️⃣ How much experience is required?
The position indicates experience comparable to 0–4 years, depending on the candidate’s relevant knowledge, skills, and qualifications.

4️⃣ What systems and tools are relevant to this role?
The role includes support for CTMS, Oracle Activate, eTMF, project trackers, study documentation systems, and other tools used for clinical trial activities.

5️⃣ What type of background is suitable for this position?
Candidates with relevant academic or vocational qualifications and experience in clinical research, clinical trial support, project coordination, documentation, or life sciences environments may be well suited.

6️⃣ What career growth opportunities can this role offer?
The position can help professionals develop experience in clinical trial operations, study coordination, project management, eTMF, CTMS, compliance, documentation, and global stakeholder management.

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