Job Tag: pharma jobs in hyderabad

Master’s qualified Pharma Data Analyst vacancy at Certara, Secunderabad. Apply now for 1-2 years experience opportunities in clinical data & pharmacology.

Clinical research is rapidly evolving, and Certara is at the forefront, accelerating drug development globally. Certara, a leader in biosimulation software and clinical pharmacology, offers an exciting opportunity for skilled professionals to join their Secunderabad office as a Data Analyst Level 1. If you are passionate about pharmacology, clinical research, and data analysis, this role provides an excellent pathway for career growth, skill enhancement, and contribution to the pharmaceutical industry’s advancement.

Company Overview

Certara is a global leader in clinical pharmacology and pharmacometrics, dedicated to accelerating medicines through innovative biosimulation software, technology, and services. Operating in over 62 countries, Certara serves more than 2,000 biopharmaceutical companies, academic institutions, and regulatory agencies. The company combines advanced simulation methodologies with extensive real-world drug development experience, ensuring clients receive accurate, reliable, and actionable insights.

Certara’s Secunderabad division is a hub for clinical data excellence, supporting meta-analyses and regulatory submissions in multiple therapeutic areas, including metabolic and cardiovascular, neuroscience, autoimmune, oncology, and respiratory diseases.

Key Highlights:

• Industry leader in clinical pharmacology & pharmacometrics.

• Supports global regulatory submissions and internal decision-making.

• Offers structured career development paths and advanced training programs.

• Committed to inclusive workplace policies and diversity.

Job Role & Responsibilities

The Data Analyst Level 1 will contribute to high-quality clinical databases supporting meta-analyses across multiple therapeutic areas. The role combines literature review, data digitization, and collaboration with peer scientists and managers to ensure accuracy and regulatory compliance.

Core Responsibilities:

• Develop and maintain clinical database products in therapeutic areas like Metabolic & CV, Neuroscience, Autoimmune, Oncology, and Respiratory.

• Analyze and annotate trial data, including study design, treatments, demographics, and outcomes (clinical, biomarker, safety, and quality of life).

• Digitize graphical data for linear, logarithmic, and semi-log scales accurately.

• Ensure data quality through consistent adherence to database rules, specifications, and quality processes.

• Collaborate with lead consultants, peer analysts, and quality managers to align with data standards.

• Participate in skill enhancement programs (statistics, R coding, systematic literature review, and data analysis methods).

• Support regulatory submissions and internal decision-making with accurate, well-curated data.

Additional Contributions:

• Work closely within a team environment, contributing to knowledge sharing and mentoring.

• Stay current on clinical research methodologies and emerging data standards.

• Uphold Certara’s corporate values: collaboration, integrity, excellence, and innovation.

Eligibility / Qualifications

Educational Requirements:

• Master’s in Pharmacology, Pharmaceutics, Clinical Practice, Public Health, Epidemiology, or PharmaD.

Preferred Experience:

• 1–2 years of experience in information science, systematic literature review, health economics, public health, or pharmaceutical industry.

Essential Skills:

• Strong understanding of pharmacology and clinical research.

• Familiarity with clinical development phases, PICOS approach, trial designs, and pharma industry data standards.

• Competency in data management tools such as R is advantageous.

• Excellent communication, collaboration, and learning skills.

• Ability to deliver high-quality, accurate data analysis consistently.

Location & Benefits

Location: Secunderabad, India
Employment Type: Full-time

Why Join Certara?

• Opportunity to contribute to global drug development initiatives.

• Structured career pathways with continuous skill development.

• Inclusive and merit-based workplace environment.

• Collaborate with leading scientists and healthcare professionals worldwide.

• Competitive remuneration and career growth opportunities.

Application Process

To apply, candidates can submit their applications directly via Certara’s career portal: Apply Here.

Important Notes:

• Certara emphasizes merit-based recruitment, free from discrimination based on race, color, religion, sex, age, or other protected characteristics.

• The company encourages candidates from diverse backgrounds to apply and provides accommodations for disabilities during the recruitment process.

• Apply promptly to secure your opportunity in a globally recognized clinical research organization.

FAQs

Q1: What is the required qualification for this role?
A: Master’s in Pharmacology, Pharmaceutics, Clinical Practice, Public Health, Epidemiology, or PharmaD.

Q2: How much experience is preferred?
A: 1–2 years in information science, systematic literature review, health economics, or pharmaceutical data analysis is ideal.

Q3: Which skills are critical for this position?
A: Pharmacology expertise, clinical research knowledge, data management skills (preferably R), analytical thinking, and strong teamwork abilities.

Q4: Is the position office-based or remote?
A: This is a full-time, office-based position located in Secunderabad, India.

Q5: How can I apply?
A: Submit your application via Certara’s official career portal: Certara Careers.

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Associate STEM Content Analyst | Clarivate Careers

Apply for Associate STEM Content Analyst at Clarivate. BPharm/MPharm/MSc graduates with 2+ years experience in clinical research. Hybrid role.

Are you a life sciences professional with a strong background in clinical research and pharmaceutical pipelines? Clarivate is inviting applications for the role of Associate STEM Content Analyst. This position is ideal for graduates in pharmacy, biotechnology, microbiology, and related life sciences who have experience in clinical research, data analysis, and content curation. Join a global leader in healthcare intelligence and contribute to advancing clinical trial insights that impact drug development worldwide.

Company Overview

Clarivate is a trusted global leader in providing actionable intelligence and analytics that accelerate innovation in the life sciences and healthcare industries. Through products like Cortellis Clinical Trial Intelligence and Drug Discovery Intelligence, Clarivate enables researchers, pharmaceutical companies, and healthcare organizations to make informed decisions that shape the future of medicine. With a commitment to accuracy, transparency, and innovation, Clarivate supports breakthroughs that improve patient outcomes and global healthcare standards.

Working at Clarivate means joining a diverse and collaborative team of experts dedicated to providing cutting-edge information solutions. Our mission is to empower innovators and ensure that clinical and scientific knowledge benefits communities worldwide.

Job Role & Responsibilities

As an Associate STEM Content Analyst, you will play a crucial role in ensuring high-quality updates and accuracy of clinical trial records. Your day-to-day responsibilities will include:

• Analyzing, cross-referencing, and updating clinical trial records from multiple sources such as company websites, press releases, conferences, and trial repositories.
• Performing secondary research to track pharmaceutical drug pipelines and trial developments.
• Maintaining awareness of ongoing developments in assigned therapeutic or technology areas.
• Recording performance metrics against defined targets.
• Supporting the team to ensure deadlines and deliverables are consistently achieved.
• Maintaining accuracy, consistency, and compliance with internal quality standards.
• Taking ownership of training and continuous professional development in new technologies.
• Participating in process improvement initiatives and adapting to workflow changes.
• Collaborating effectively with content specialists, senior analysts, and cross-functional stakeholders.

This role is an opportunity to combine your scientific expertise with data-driven content analysis, contributing to Clarivate’s global knowledge platforms that power pharmaceutical and biotech innovations.

Eligibility / Qualifications

To be successful in this role, candidates must meet the following requirements:

• Education: BPharm, MPharm, M.Sc in Biotechnology, Microbiology, Life Sciences, or related fields.
• Experience: Minimum 2 years of experience in analyzing and updating clinical trial reports.
• Strong knowledge of clinical trials, pharmaceutical drug pipelines, drug development, and clinical phases.
• Excellent English communication skills (both written and verbal).
• Proficiency in content analysis, research methodologies, and handling multiple data sources.

Preferred Skills:

• Experience in secondary research related to clinical trial or pharmaceutical data.
• Strong analytical ability to delve deep into trial results and interpret scientific content.
• Effective planning and time management skills.
• Flexibility to adapt to changing processes and project requirements.

Relevant Courses: BPharm, MPharm, M.Sc Biotechnology, M.Sc Microbiology, M.Sc Life Sciences, Clinical Research, Pharmaceutical Sciences

Location & Salary

• Work Mode: Hybrid (remote flexibility available)
• Locations: Available across 2 locations (specific office locations shared during recruitment process)
• Work Hours: Full-time, 8 hours per day, Monday to Friday
• Employment Type: Permanent
• Salary: Competitive, aligned with industry standards, plus employee benefits and career development opportunities

Application Process

If you are passionate about clinical research content analysis and want to be part of a global healthcare intelligence provider, apply today.

• Apply Here: Clarivate Careers Portal
• Job ID: JREQ133450

Early applications are encouraged as shortlisting is in progress. Apply before the closing date to secure your chance to join Clarivate’s expert content team.

FAQs

Q1: What qualifications are required for this role?
A1: Candidates should hold BPharm, MPharm, or M.Sc in Biotechnology, Microbiology, Life Sciences, or equivalent fields, with at least 2 years of clinical data analysis experience.

Q2: Is this a remote job?
A2: The role is hybrid, offering a balance of remote work flexibility and office-based collaboration.

Q3: What kind of work will I be doing?
A3: You will analyze and update clinical trial records, track pharmaceutical pipelines, and ensure high-quality content for Clarivate’s clinical trial intelligence products.

Q4: Does Clarivate provide equal opportunities?
A4: Yes, Clarivate is an equal opportunity employer, committed to diversity and inclusion in all aspects of employment.

Q5: What is the team structure like?
A5: You will be working with a 20-member team consisting of content specialists, senior analysts, and associate analysts supporting Cortellis Clinical Trial Intelligence and Drug Discovery Intelligence.

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Regulatory Coordinator Vacancy for Science Graduates | Novartis Hyderabad
Apply for Regulatory Coordinator position at Novartis, Hyderabad. Open for Science, Pharmacy, Biotechnology graduates with 3-5 years’ experience.

Join one of the world’s leading pharmaceutical companies, Novartis, as a Regulatory Coordinator in Hyderabad, India. This role offers science and pharmacy graduates the opportunity to contribute to global healthcare by supporting regulatory submissions, license renewals, and compliance activities. If you’re looking to make an impact in pharmaceutical regulatory affairs, this could be your ideal career move.

Company Overview

Novartis is a global leader in pharmaceuticals with a clear purpose: to reimagine medicine and improve patients’ lives. With operations spanning more than 100 countries, Novartis focuses on innovation, research, and advancing healthcare. Employees at Novartis thrive in a culture built on diversity, inclusivity, and collaboration. Every associate contributes to breakthroughs that transform how patients are treated worldwide.

Job Role & Responsibilities

As a Regulatory Coordinator, you will:

• Contribute to the development and submission of product registrations, amendments, and periodic reports.
• Procure key regulatory documents such as GMP certificates, COAs, and registration samples.
• Collaborate with global and regional stakeholders (USFDA, EMA, Swissmedic, NTO, RA Ops, Tech Ops).
• Support timely planning and delivery of regulatory documents for license renewals, site transfers, and new submissions.
• Represent the Regulatory Affairs LCM BOE team in project and team meetings.
• Ensure compliance with regulatory policies, global standards, and internal procedures.
• Track project timelines, monitor dossier progress, and maintain updated regulatory country requirements.
• Contribute to cross-functional excellence initiatives and training activities.

This role is central to ensuring regulatory readiness and compliance, directly impacting patient safety and global healthcare access.

Eligibility / Qualifications

To qualify, you must have:

• Educational Background: Bachelor’s or Master’s degree in Pharmacy, Chemistry, Biochemistry, Biotechnology, Biology, Life Sciences or related field.
• Experience: 3–5 years in Regulatory Affairs or pharmaceutical industry roles.
• Strong understanding of global pharmaceutical regulations.
• Excellent communication and interpersonal skills.
• Proven ability to prioritize and work effectively in matrix teams.
• Fluency in English (written and spoken).

Preferred additional skills include:

• Knowledge of global dossier submissions, RA operations, and compliance processes.
• Hands-on experience collaborating with regulatory agencies and multinational project teams.

Location & Salary

• Location: Hyderabad (Office), India
• Company/Legal Entity: Novartis Healthcare Private Limited
• Division: Development
• Functional Area: Research & Development
• Employment Type: Full-time, Regular
• Shift Work: No

Application Process

Interested candidates can apply directly via the Novartis careers portal. Ensure you apply early to secure your spot!

👉 Apply Here

FAQs

Q1: Who can apply for this role?
Candidates with a degree in Pharmacy, Chemistry, Biochemistry, Biotechnology, Biology, or Life Sciences and 3–5 years of regulatory/pharma experience.

Q2: What are the main responsibilities of a Regulatory Coordinator at Novartis?
The role includes supporting submissions, renewals, document procurement, compliance, and cross-functional collaboration for global markets.

Q3: Where is this role based?
The position is based in Hyderabad, India at Novartis Healthcare Private Limited.

Q4: What benefits will I receive?
Novartis offers competitive pay, professional development, diversity-friendly policies, and access to the Novartis Life Handbook for rewards and benefits.

Q5: Is this a full-time role?
Yes, it is a full-time, regular position with no shift work.

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