Job Tag: Pharma Jobs in Mumbai

Drug Safety Specialist/Clinical Safety Coordinator – Navi Mumbai, 2025 nikki woods nudes livealittlebud

Apply for Drug Safety Specialist/Clinical Safety Coordinator at Medpace, Navi Mumbai. Bachelor’s degree required. 2025 vacancies open.

Medpace, a globally recognized full-service Clinical Research Organization (CRO), is inviting applications for the role of Drug Safety Specialist/Clinical Safety Coordinator in Navi Mumbai, India. This position provides an exciting opportunity to contribute to clinical safety, pharmacovigilance, and post-marketing surveillance while building a rewarding career in clinical research.

Company Overview

Medpace is a leading clinical CRO providing Phase I-IV development services to the biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, with over 5,000 employees across 40+ countries, Medpace leverages local regulatory and therapeutic expertise in oncology, cardiology, metabolic disease, endocrinology, CNS, anti-viral, and anti-infective areas. The company emphasizes scientific rigor, discipline, and a mission to accelerate the global development of safe and effective medical therapeutics.

Why Work at Medpace?

• People, Purpose, Passion: Join a team dedicated to making a difference in patient lives worldwide.
• Impactful Work: Contribute to advancing therapies across multiple therapeutic areas.
• Recognition & Awards: Forbes-recognized for midsize company excellence; multiple CRO leadership awards.
• Career Growth: Structured career paths, employee appreciation events, health and wellness initiatives.
• Flexible Work Environment: Encouraging work-life balance and professional development.

Job Role & Responsibilities

As a Drug Safety Specialist/Clinical Safety Coordinator, you will play a critical role in handling adverse events, supporting pharmacovigilance activities, and ensuring compliance with clinical safety processes. Key responsibilities include:

• Determining the appropriate plan of action for incoming calls regarding adverse events.
• Collecting, processing, and tracking incoming adverse and serious adverse events from clinical trials and post-marketing surveillance.
• Writing clear and comprehensive safety narratives.
• Reporting and analyzing safety data to ensure timely regulatory submission.
• Collaborating with internal departments and investigative clinical research sites to maintain compliance with safety processes.

Eligibility / Qualifications

• Education: Bachelor’s degree in Healthcare-related fields such as Nursing, Pharmacy, Pharmacology, or related disciplines.
• Experience: Clinical experience, clinical research, case processing, and post-marketing pharmacovigilance preferred.
• Skills:
  • Proficient English communication (written and verbal)
  • Strong knowledge of medical terminology
  • Proficiency in Microsoft Office Suite
  • Strong organizational, analytical, and communication skills

Relevant Courses: B.Pharm, M.Pharm, Pharm.D, Nursing, Clinical Research, Biotechnology, Life Sciences.

Location & Salary

• Location: Navi Mumbai, Maharashtra, India (Office-based)
• Salary: Competitive, commensurate with qualifications and experience. Additional benefits include flexible work arrangements, health initiatives, and PTO packages.

Application Process

Interested candidates can apply online via Medpace’s official careers portal: Apply Here. Ensure your resume highlights relevant education, skills, and pharmacovigilance experience to enhance your chances. Apply promptly to secure your opportunity!

FAQs

Q1: Can freshers apply for this role?
A1: Freshers with relevant healthcare education and interest in pharmacovigilance may apply, though prior clinical experience is preferred.

Q2: What is the required qualification?
A2: Bachelor’s degree in Nursing, Pharmacy, Pharmacology, or related healthcare fields.

Q3: Is this a remote position?
A3: No, the role is office-based in Navi Mumbai.

Q4: What skills are necessary?
A4: Strong communication, medical terminology knowledge, Microsoft Office proficiency, and attention to detail.

Q5: How many vacancies are open?
A5: Multiple vacancies (2025) are currently open for eligible candidates.

Why This Role Matters

Joining Medpace as a Drug Safety Specialist/Clinical Safety Coordinator provides an impactful career path in clinical research and pharmacovigilance. You will contribute directly to patient safety, regulatory compliance, and the advancement of medical therapeutics globally. The role ensures continuous professional development while making a meaningful difference in healthcare outcomes.

Take the first step toward a rewarding pharmacovigilance career—apply today!

Vertical Summary Table

Apply now for Sun Pharma Data Coordinator (Clinical Trials) role in Mumbai. 5+ years’ experience in clinical data management required.

As one of the world’s leading pharmaceutical companies, Sun Pharma is hiring a Data Coordinator (Clinical Trials) at its corporate office in Mumbai. This role offers experienced clinical data professionals an exciting opportunity to contribute to high-impact global research programs.

At Sun Pharma, we believe in empowering our people to “Create Your Own Sunshine.” Join us and become part of a collaborative, innovation-driven culture that helps you grow personally and professionally while making a real difference in patient outcomes worldwide.

Company Overview

Sun Pharmaceutical Industries Ltd. is the fourth largest specialty generic pharmaceutical company globally and India’s most valuable pharma brand by market capitalization. Operating across more than 150 countries, Sun Pharma delivers affordable, high-quality medicines trusted by healthcare professionals and patients worldwide.

The company’s strong research and development division focuses on clinical research, regulatory sciences, and innovation that advance global healthcare. By joining Sun Pharma, you become part of an organization recognized for excellence, growth opportunities, and long-term career stability.

Job Role & Responsibilities

As a Data Coordinator (Clinical Trials), you will support critical aspects of clinical research data management. Your role ensures accuracy, compliance, and timely delivery of data for global submissions and regulatory approvals.

Key Responsibilities include:

• Prepare and review startup documents: eCRF Completion Guidelines, Data Management Plan (DMP), SAE Reconciliation Plan, Clinical Coding Plan.

• Develop Edit Specification Documents (ESD), Test Plans, and Data Entry Guidelines.

• Perform screen design UAT and edit check UAT in CDMS as per ESD.

• Manage discrepancies and ensure accurate query resolution.

• Support Data Manager in reviewing URS for IWRS.

• Ensure timely completion of SAE reconciliation and database lock activities.

• Prepare and update Master Data Management Files for completeness.

• Draft and review Data Management Reports (DMRs).

Eligibility / Qualifications

Educational Background:

• Postgraduate degree in Pharmacy, Life Sciences, Biotechnology, Clinical Research, or related fields.

Experience:

• Minimum 5 years’ experience in clinical data management within Pharma or CRO industry.

Additional Skills:

• Strong knowledge of data management documents, validation plans, screen UAT, edit check UAT, and clinical data query management.

• Excellent attention to detail, communication skills, and ability to work cross-functionally.

Location & Salary

Work Location: Sun House – Corporate Office, Mumbai.
Salary: Competitive industry package with benefits (not disclosed in posting).

Employees enjoy career development opportunities, health benefits, and a collaborative work environment where innovation is encouraged.

Application Process

Interested professionals can apply directly via the official Sun Pharma careers portal:
👉 Apply Here

⏳ Apply early to secure your chance to join India’s top pharmaceutical organization.

FAQs

Q1. What qualifications are required for the Data Coordinator role?
A postgraduate degree in pharmacy, life sciences, biotechnology, or related fields is mandatory.

Q2. How many years of experience are needed?
A minimum of 5 years’ clinical data management experience in Pharma or CRO industry.

Q3. Is this a work-from-home role?
No, this is a work-from-office role based in Mumbai at Sun Pharma’s corporate office.

Q4. What are the growth opportunities?
Sun Pharma offers excellent career progression in clinical research, data management, and regulatory operations.

Q5. How can I apply?
Applications must be submitted via the official Sun Pharma careers portal.

Vertical Summary Table

Regulatory Affairs Associate I – Teva Pharma Hiring, Navi Mumbai

Apply for Regulatory Affairs Associate I at Teva Pharmaceuticals, Navi Mumbai. B.Pharm/M.Pharm/Life Sciences graduates with 2–3 years experience preferred.

Teva Pharmaceuticals, the world’s leading manufacturer of generic medicines, is seeking a Regulatory Affairs Associate I for its Navi Mumbai facility. This full-time role offers an exciting opportunity to contribute to global regulatory publishing activities, ensuring timely, accurate, and compliant submissions for EU, US, and Canadian markets. If you are a pharmacy or life sciences graduate with regulatory publishing experience, this role could be your gateway to a rewarding career in regulatory affairs.

Company Overview

Teva Pharmaceuticals is on a mission to make good health more affordable and accessible. Operating in nearly 60 countries, Teva supplies medicines to 200 million people worldwide every day. The company is a proud producer of many products listed on the World Health Organization’s Essential Medicines List. With a rich heritage in generics, innovative specialty medicines, and biosimilars, Teva combines global expertise with local insights to improve healthcare worldwide.

Joining Teva means being part of a diverse team, committed to delivering excellence, innovation, and patient access to essential therapies.

Job Role & Responsibilities

As a Regulatory Affairs Associate I – RA, you will:

• Responsible for executing GRO Regulatory Data Analytics operations in line with Work Instructions and SOPs. Primarily will be Regulatory Data Analytics Service related to product registration data management (includes the procurement of data from source regulatory documentation which requires a thorough understanding of the structure and contents of a regulatory dossier, and a thorough understanding of the data structures applicable to registration data and the related system workflows).
• Operationally hands-on in terms of carrying out data management activities as an individual contributor. This will require a thorough understanding of the structure and contents of a regulatory dossier (i.e. will be fluent in navigating and understanding the contents of a dossier). Registration data management will require a thorough understanding of the registration data structures, workflows, and applicable work instructions etc.
• Perform Quality Control (QC) and data integrity checking, as part of the Regulatory Data Analytics operation, to confirm the accuracy and completeness of the Teva Global Registration database.
• Represent GRO Regulatory Data Analytics across the wider Global Regulatory Affairs community. Must be proficient at building effective working relationships with all stakeholder and customer groups.
• Responsible for providing effective business project contributions for projects focused on improving regulatory data quality, the provisioning of regulatory data for internal re-use via system integration, or the implementation of any business or technology change that impacts regulatory data or the regulatory technology landscape.

Eligibility / Qualifications

Education:

• Masters in Pharmacy or Masters in Science/Life Sciences
• College or University degree or equivalent work experience that provide knowledge of and exposure to fundamental theories, principles and concepts.

Experience:

• Required: Bachelor’s or Master’s degree in Life Sciences or Information Technology.
• Preferred: MS in a scientific or information technology discipline

Minimum Years of Work Experience:

• Required: 1–3 years (preferably with experience in regulatory operations/affairs).

Location & Salary

• Location: Navi Mumbai, Maharashtra, India – 400706
• Work Model: Full-time, onsite
• Compensation: Competitive salary based on experience, with industry-standard benefits
• Reporting To: Manager – Regulatory Submission Management

Application Process

Interested candidates can apply directly via Teva’s official career portal:
Apply Here

Safety Writer Vacancy – Life Sciences Graduates | Mumbai

Apply for Safety Writer position at Fortrea, Mumbai. Open for life sciences graduates with 3+ years’ experience in medical writing.

Are you an experienced medical writer passionate about patient safety and regulatory compliance? Fortrea, a global leader in clinical development, is hiring a Safety Writer in Mumbai. This role offers the opportunity to work on critical safety documentation, collaborate with cross-functional teams, and contribute to global regulatory submissions. If you are ready to make a meaningful impact in the healthcare and pharmaceutical sector, this could be your next career move.

Company Overview

Fortrea is a trusted name in the pharmaceutical, biotech, and clinical research industry, known for delivering end-to-end clinical development and post-approval solutions. With a strong emphasis on pharmacovigilance, regulatory writing, and clinical trial support, Fortrea empowers life sciences organizations to accelerate the delivery of safe and effective treatments to patients worldwide.

Our teams are driven by science, innovation, and a commitment to patient-centric healthcare solutions. Joining Fortrea means working in an environment that values expertise, collaboration, and continuous professional development.

Job Role & Responsibilities

As a Safety Writer at Fortrea, you will:

• Prepare and review aggregate safety reports, risk management documents, and signal detection reports.
• Lead client communication and manage timelines for assigned reports.
• Provide oversight, quality checks, and mentoring support to junior safety writers.
• Conduct literature searches, analyze findings, and incorporate insights into reports.
• Author various safety and regulatory documents including:
  • Periodic Safety Update Reports (PSURs)
  • Development Safety Update Reports (DSURs)
  • Periodic Adverse Drug Experience Reports (PADERs)
  • Risk Management Plans (RMPs)
  • Clinical Study Summaries and CTD modules
• Prepare narratives for adverse drug reactions (ADRs) and serious adverse events (SAEs).
• Collaborate with cross-functional teams and external stakeholders to ensure compliance with ICH-GCP, pharmacovigilance guidelines, and global regulations.
• Contribute to label updates, literature abstracts, and medical information documents.
• Promote efficient, high-quality processes to ensure on-time regulatory submissions.

Eligibility / Qualifications

Minimum Requirements:

• Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Biochemistry, Microbiology, Clinical Research, or related fields.
• At least 3 years of pharmaceutical industry experience, with 2+ years in medical or safety writing.
• Strong command over written and spoken English.
• Proficiency in MS Office tools.
• Excellent organizational and time management skills.
• Solid understanding of pharmacovigilance practices, ICH-GCP guidelines, and regulatory compliance.

Preferred Qualifications:

• Master’s or PhD in life sciences or related field.
• Prior experience in clinical research or scientific writing.
• Familiarity with signal detection, benefit-risk evaluation, and global regulatory frameworks.

Location & Work Environment

• Location: Mumbai, India
• Work Type: Full-time
• Travel: Up to 5% (domestic or international as project needs demand)
• Flexible, collaborative, and diverse work culture supporting employee well-being and career growth.

Application Process

Interested candidates can apply directly through the Fortrea careers portal:

👉 Apply Here

Apply before the closing date: September 26, 2025.

Don’t miss the chance to work with a global leader in safety writing and pharmacovigilance. Apply today to secure your spot!

FAQs

Q1. What qualifications are required for the Fortrea Safety Writer role?
A Bachelor’s degree in life sciences or related fields with at least 3 years of experience in pharma/medical writing.

Q2. Is prior clinical research experience mandatory?
It is desirable but not mandatory. Equivalent industry experience will be considered.

Q3. What types of reports will I be working on?
You will work on PSURs, DSURs, PADERs, RMPs, CTD summaries, and safety narratives.

Q4. Does the role require travel?
Yes, up to 5% of travel (domestic or international) may be required.

Q5. When is the application deadline?
Applications close on September 26, 2025.

Summary Table

CRA I/II Vacancy – Clinical Research Associate | ICON – Mumbai

Apply for CRA I/II Clinical Research Associate role at ICON, Mumbai. Bachelor’s degree & 3+ years’ experience required. Competitive salary & benefits.

ICON plc, a global leader in healthcare intelligence and clinical research, is hiring Clinical Research Associate (CRA I/II) professionals for its Mumbai office. This is a high-impact opportunity for skilled clinical research professionals to advance their careers while contributing to innovative therapies and the future of drug development. If you’re passionate about clinical monitoring and ensuring patient safety, this could be your next big step.

Company Overview

ICON plc is one of the world’s leading Clinical Research Organizations (CROs), providing outsourced development and commercialisation services to pharmaceutical, biotechnology, and medical device industries. With a strong focus on innovation, inclusion, and global healthcare improvement, ICON plays a pivotal role in designing and executing clinical trials that bring life-changing treatments to patients worldwide.

Job Role & Responsibilities

As a Clinical Research Associate I/II, you will be responsible for:

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring compliance with trial protocols, data integrity, and patient safety.
• Collaborating with investigators, site staff, and internal teams to ensure smooth study operations.
• Performing data review and resolving queries to maintain high-quality clinical trial data.
• Supporting preparation and review of essential study documentation, protocols, and reports.

Eligibility / Qualifications

• Education: Bachelor’s degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Microbiology, Biochemistry, or related healthcare fields.
• Experience: Minimum of 3 years as a Clinical Research Associate with strong on-site monitoring experience.
• Domain Expertise: Oncology/Immunology therapeutic area expertise is mandatory.
• Skills:
  • Strong organizational and communication skills.
  • In-depth knowledge of ICH-GCP and clinical trial regulations.
  • Ability to work independently in a fast-paced environment.
• Other Requirements:
  • Ability to travel up to 60% (domestic and international).
  • Valid driver’s license.

Location & Salary

• Location: Mumbai, India (Office-Based)
• Salary: Competitive industry package along with attractive benefits.

Benefits at ICON

• Competitive salary & performance-based rewards.
• Generous leave entitlements.
• Health insurance plans for employees and family.
• Retirement and financial planning programs.
• Employee assistance programs (24/7 access to global professionals).
• Life assurance.
• Flexible optional benefits such as gym discounts, travel subsidies, health assessments, and childcare vouchers.

Application Process

Apply directly through ICON’s career site to be considered:
👉 Apply Here

Act fast – applications are reviewed on a rolling basis. Don’t miss your chance to join one of the most trusted names in global clinical research.

FAQs

1. What is the eligibility for CRA I/II role at ICON in Mumbai?
A bachelor’s degree in life sciences or healthcare and at least 3 years of CRA experience with oncology/immunology expertise.

2. Does ICON provide training for CRA roles?
Yes, ICON invests in continuous learning and development through structured training programs.

3. What is the salary range for CRA jobs in India?
While not disclosed, ICON offers competitive salaries with industry-leading benefits.

4. Is travel required for this position?
Yes, up to 60% domestic and international travel is required.

5. Why join ICON plc?
ICON is globally recognized for clinical research excellence, diversity, and employee growth opportunities.

Quick Job Summary

Safety Database Specialist | Life Sciences Graduate | Navi Mumbai

Apply for Medpace Safety Database Specialist role in Navi Mumbai. Life Sciences or Informatics graduates with Argus, SQL, OBIEE experience preferred.

Join Medpace in Navi Mumbai as a Safety Database Specialist and contribute to advancing global clinical research. This role is designed for skilled graduates in Life Sciences, Pharmacy, or Business Informatics who want to build a strong career in pharmacovigilance systems, Argus safety databases, and clinical safety reporting. With Medpace’s reputation as a top global CRO, this opportunity offers professional growth, international exposure, and meaningful contributions to drug safety.

Company Overview

Medpace is a global, full-service clinical contract research organization (CRO) supporting the biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, Medpace operates in 40+ countries with 5,000+ employees. We specialize in Phase I-IV clinical development and therapeutic expertise spanning oncology, cardiology, endocrinology, infectious diseases, CNS, and more.

With a mission to accelerate drug development through scientific and disciplined processes, Medpace has been consistently recognized by Forbes and awarded CRO Leadership Awards for quality, reliability, and expertise.

Job Role & Responsibilities

As a Safety Database Specialist, you will play a vital role in Medpace’s Clinical Safety team. Your day-to-day work ensures the smooth functioning of global pharmacovigilance systems, contributing directly to patient safety and regulatory compliance.

Key responsibilities include:

• Configure Argus and Argus J systems, including product, study, and license setup.
• Generate regulatory and periodic safety reports (DSUR, PSUR, PBRER).
• Support audits and inspections by ensuring high data accuracy and compliance.
• Develop SOPs, Work Instructions, and manuals for database processes.
• Assist in user acceptance testing (UAT) for safety system changes.
• Provide Argus database training for new users.
• Support global safety operations through SQL queries and OBIEE reporting tools.
• Troubleshoot and resolve safety database-related issues efficiently.

Eligibility / Qualifications

Minimum Requirements:

• Bachelor’s degree in Life Sciences, Pharmacy, Business Informatics, Biotechnology, or a related discipline.
• 1–2 years of experience in pharmacovigilance, CRO, biotech, or pharma industry.

Preferred Skills:

• Hands-on experience with Argus and Argus J safety systems.
• Knowledge of SQL and reporting/analytics platforms like OBIEE.
• Familiarity with study configurations in safety systems.
• Strong problem-solving, client service, and consultative skills.
• Prior experience with safety system audits and compliance processes.

Location & Salary

• Location: Navi Mumbai, India
• Salary & Benefits: Competitive compensation with a comprehensive benefits package, flexible work environment, employee wellness initiatives, and structured career growth.

Why Medpace?

• Recognized by Forbes (2021–2024) among America’s Most Successful Midsize Companies.
• CRO Leadership Awards for quality, expertise, and compatibility.
• 30+ years of clinical development experience, improving patient outcomes worldwide.
• Opportunities for cross-functional learning and professional advancement.
• A collaborative and employee-focused culture with health, wellness, and appreciation programs.

Application Process

Interested candidates can apply directly through the official Medpace career portal: Apply Here.

Apply soon to secure your chance at this career-defining opportunity with one of the world’s leading CROs.

FAQs

Q1: Who can apply for the Medpace Safety Database Specialist role?
Candidates with a Bachelor’s in Life Sciences, Pharmacy, Biotechnology, or Business Informatics with 1–2 years of PV database experience are eligible.

Q2: What technical expertise is required?
Hands-on experience in Argus/Argus J, SQL, OBIEE, and safety system configurations is preferred.

Q3: Is prior CRO/pharma experience necessary?
Yes, prior experience in CRO, pharma, or biotech industries is highly valued.

Q4: What benefits does Medpace offer?
Medpace offers competitive pay, flexible work settings, PTO, employee wellness initiatives, and structured career growth opportunities.

Q5: How do I apply?
You can apply via the official Medpace career portal link provided above.

Vertical Summary Table

Medtronic hiring Clinical Research Coordinator in Mumbai. Apply now for a full-time role with 4+ years’ experience requirement.

Medtronic, a global leader in healthcare technology, is inviting applications for the position of Clinical Research Coordinator in Mumbai. This full-time role offers the opportunity to support innovative clinical studies while working with one of the world’s most respected med-tech companies. If you have 4+ years of experience in clinical research operations and want to contribute to groundbreaking healthcare advancements, this is the perfect opportunity.

Company Overview

Medtronic is the world’s largest medical technology company, employing over 95,000 professionals across 150 countries. With a mission to alleviate pain, restore health, and extend life, Medtronic focuses on developing transformative healthcare solutions that impact millions of lives globally. Their culture encourages innovation, collaboration, and continuous professional development, making it a preferred employer for clinical research professionals.

Job Role & Responsibilities

As a Clinical Research Coordinator, you will play a key role in supporting clinical studies and ensuring compliance with protocols. Responsibilities include:

• Data Coordination:
  • Develop and test case report forms, study databases, and study reports.
  • Ensure timely and accurate data entry and verification.
  • Manage and resolve data discrepancies.
• Document Coordination:
  • Create and maintain clinical study files.
  • Organize and distribute study-related documents.
  • Assist with audits to ensure completeness and compliance.
• Operational Support:
  • Provide organizational and administrative support to clinical teams.
  • Support special projects and cross-functional initiatives.
  • Propose solutions to process improvements and workflow challenges.
• Mentorship & Training:
  • Guide, coach, and provide training to junior employees.

Eligibility / Qualifications

• Education: Graduate or Postgraduate degree in Life Sciences, Pharmacy, Nursing, Biotechnology, or related fields.
• Experience: Minimum of 4 years of relevant experience in clinical research coordination, clinical operations, or data management.
• Skills Required:
  • Strong knowledge of GCP guidelines and clinical trial regulations.
  • Proficiency in handling clinical trial documentation and data systems.
  • Good communication and interpersonal skills.
  • Problem-solving mindset with ability to work independently.

Location & Salary

• Job Location: Mumbai, Maharashtra, India
• Compensation: Competitive salary with performance-based incentives.
• Benefits: Comprehensive benefits package, flexible work options, health insurance, retirement plans, and career development support.

Application Process

Interested candidates can apply directly through Medtronic’s official careers portal:
👉 Apply Here

📅 Apply early to ensure consideration for this prestigious role.

Why Join Medtronic?

• Be part of the world’s leading medical technology company.
• Contribute to life-saving innovations and breakthrough therapies.
• Access structured career growth and global exposure.
• Work in an inclusive, diverse, and innovation-driven culture.

FAQs

1. What is the minimum experience required?
A minimum of 4 years of relevant experience is required.

2. What is the job location?
The position is based in Mumbai, Maharashtra, India.

3. What qualifications are preferred?
Graduates or postgraduates in Life Sciences, Pharmacy, Biotechnology, or Nursing are eligible.

4. Is prior clinical research experience mandatory?
Yes, experience in clinical research or clinical trial coordination is essential.

5. What benefits does Medtronic offer?
Medtronic provides a competitive salary, flexible benefits, and global career advancement opportunities.

Summary Table