Associate STEM Content Analyst

Lifelancer; Hyderabad; On-site; INR 300,000 - 420,000; Full time

Job summary

A clinical research organization in Hyderabad is seeking an Associate STEM Content Analyst to join their Clinical Studies team. This entry-level role involves maintaining accurate clinical trial information and involves collaboration within a skilled team. Candidates should have a BPharma or related degree and be proficient in English communication. The position is hybrid, offering flexibility while ensuring accountability for weekly targets and quality standards.

Qualifications

• Freshers or 6 months of experience in analyzing and updating clinical reports.
• In-depth knowledge of clinical trials, pharmaceutical drug pipelines, drug development, and clinical phases.
• In-depth knowledge of clinical trials and drug development.
• Excellent English written and verbal communication skills.

Responsibilities

• Actively seek out information about Clinical Studies and update information in clinical records.
• Maintain Clarivate database with accurate Clinical trials information.
• Accountable for the delivery of weekly targets.
• Ensure quality standards are observed.
• An inquisitive, analytical mind with strong problem‑identification and solving skills

Skills

English written and verbal communication skills

Analytical skills

Knowledge of clinical trials

Education

BPharma/M Pharma/MSc in Biotechnology or Microbiology

Job description

Job Title: Associate STEM Content Analyst

Job Location: 9F6G+9F9, Charminar Rd, Chowk Mohammed Khan, Chow Mohalla, Pathar Gatti, Hyderabad, Telangana 500002, India

Job Location Type: Hybrid

Job Contract Type: Full-time

Job Seniority Level: Entry level

We are looking for an Associate Content Editor to join our Clinical Studies team in Hyderabad. This is an amazing opportunity to work on Cortellis Clinical Trial Intelligence and Cortellis Drug Discovery Intelligence. The team consists of 20 people and we have a great skill set in Clinical. We would love to speak with you if you have skills in Clinical/Drugs.

Responsibilities

As an Associate Content Editor in the Clinical team, you will be responsible for actively seeking out information about Clinical Studies, analyzing, cross‑referencing, and updating all new or previously updated information in the clinical records from various sources, which includes scientific meetings, conferences, trial registries, press releases and other possible internet sources.

About You – Experience, Education, Skills, And Accomplishments

• Education (BPharma/M Pharma/MSc in Biotechnology, Microbiology)
• Freshers or 6 months of experience in analyzing and updating clinical reports
• In‑depth knowledge of clinical trials, pharmaceutical drug pipelines, drug development and clinical phases
• Excellent English written and verbal communication skills

It would be great if you also had

• Experience in secondary research related to clinical information

What will you be doing in this role?

• Maintain Clarivate database with up‑to‑date and accurate Clinical trials information from a range of information sources
• Accountable for the delivery of weekly targets
• Ensure quality standards are observed
• Ability to understand and interpret complex and detailed Trials & Drugs related information from source material
• An inquisitive, analytical mind with strong problem‑identification and solving skills

Hours of Work

9:00 AM to 6:00 PM

Work mode: Hybrid (Monday to Friday)

Location: Hyderabad

At Clarivate, we are committed to providing equal employment opportunities for all qualified persons with respect to hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. We comply with applicable laws and regulations governing non‑discrimination in all locations.