Remote Clinical Research Associate Hiring at Thermo Fisher

Clinical Research Associate Openings for Life Science Graduates | Remote India

Apply for CRA Level I–Sr CRA roles for BSc, MSc, BPharm graduates. Remote India positions with Thermo Fisher Scientific.

Thermo Fisher Scientific is hiring Clinical Research Associates (CRA Level I, Level II and Senior CRA) for its clinical operations team in India. These remote full-time openings are suited for candidates with hands-on clinical monitoring experience and a solid background in life sciences or nursing. This role supports global clinical trials across therapeutic areas, helping advance drug development with accuracy, compliance, and high scientific standards.

Company Overview

Thermo Fisher Scientific is a global leader in scientific research, laboratory solutions, and clinical development services. Through its PPD clinical research portfolio, the company supports studies in more than 100 countries and provides end-to-end clinical trial services. The organization is known for its strong commitment to scientific integrity, patient safety, and regulatory compliance. Professionals working here contribute to the development of life-changing therapies and the improvement of health outcomes worldwide.

Job Role & Responsibilities

As a Clinical Research Associate, you will manage clinical monitoring and site oversight activities to ensure trial compliance, data accuracy and audit readiness.

Key Responsibilities

• Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks.
• Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities.
• Assess investigational products through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards.
• Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution.
• May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner.
• Conducts monitoring tasks in accordance with the approved monitoring plan. Participates in the investigator payment process.
• Ensures a shared responsibility with other project team members on issues/findings resolution. Investigates and follows-up on findings as applicable.
• Participates in investigator meetings as necessary. Identifies potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites.
• Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted.
• Performs trial close out and retrieval of trial materials.
• Ensures that required essential documents are complete and in place, according to ICH-GCP and applicable regulations.
• Conducts on-site file reviews as per project specifications.
• Provides trial status tracking and progress update reports tothe Clinical Team Manager (CTM) as required.
• Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial Management System).
• Facilitates effective communication between investigative sites, the client company and the PPD project team through written, oral and/or electronic contacts.
• Responds to company, client and applicable regulatory requirements/audits/inspections.
• Maintains & completes administrative tasks such as expense reports and timesheets in a timely manner.
• Contributes to the project team by assisting in preparation of project publications/tools, and sharing ideas/suggestions with team members.
• Contributes to other project work and initiatives for process improvement, as required.
• Job Complexity Works on problems of limited scope. Follows standard practices and procedures in analyzing situations or data from which answers can be readily obtained.
• Job Knowledge Learns to use professional concepts. Applies company policies and procedures to resolve routine issues.
• Supervision Received Normally receives detailed instructions on all work.
• Business Relationships Contacts are primarily with immediate supervisor, and other personnel in the department. Builds stable working relationships internally.

Eligibility / Qualifications

Education

• Bachelor’s degree in a life science field (BSc Biotechnology, BSc Microbiology, BSc Biochemistry, BSc Life Sciences) or equivalent.
• BPharm, MPharm, MSc Life Sciences, or Registered Nursing certification also accepted.

Experience

• Minimum 2+ years of onsite clinical monitoring experience.
• Strong working knowledge of ICH-GCP and clinical research regulations.

Skills & Competencies

• Proven clinical monitoring ability.
• Solid understanding of medical terminology and therapeutic areas.
• Strong communication and documentation skills.
• High attention to detail and accuracy.
• Organizational and time-management strength.
• Ability to work independently and within cross-functional teams.
• Proficiency in Microsoft Office and willingness to learn new software.

Location & Salary

Location

• Remote, India (Full-time, standard Monday–Friday schedule).

Work Environment

• Office-based remote structure.
• Requires regular communication with diverse groups.
• Includes independent travel for monitoring visits.
• Exposure to healthcare or laboratory environments may occur.
• Must work efficiently under pressure while managing multiple priorities.

Application Process

Eligible candidates can apply directly via the company career portal. Ensure your resume highlights clinical monitoring experience, therapeutic exposure and familiarity with ICH-GCP.

Apply Here: https://jobs.thermofisher.com/global/en/job/R-01326248/CRA-Level-I-Level-II-and-Sr-CRA

---

FAQs

1. Who can apply for the CRA roles?

Candidates with BSc, MSc, BPharm, MPharm, Nursing or equivalent life science qualifications with at least 2 years of monitoring experience.

2. Is this a remote position?

Yes. The role is fully remote within India but involves travel for site visits.

3. What skills are required for a CRA position?

Strong knowledge of ICH-GCP, communication skills, risk-based monitoring, document accuracy and site management capabilities.

4. Does Thermo Fisher accept candidates from biotech or nursing backgrounds?

Yes. Biotechnology, Microbiology, Nursing, Pharmacy and Life Science graduates are eligible.

5. How do I apply?

Submit your application through the official Thermo Fisher job link provided above.

---

Summary Table

Category	Details
Company	Thermo Fisher Scientific
Vacancies	CRA Level I, Level II, Senior CRA
Required Education	BSc Biotechnology, BSc Microbiology, BSc Biochemistry, BSc Life Sciences, BPharm, MPharm, MSc Life Sciences, Nursing certification
Experience	Minimum 2+ years of onsite clinical monitoring experience

Tagged as: Pharma Jobs in Bangalore