Are you a B.Pharm, M.Pharm, B.Sc, or M.Sc graduate eager to build a career in the pharmaceutical industry? Kshirvaid Lifesciences Pvt. Ltd., a trusted name in international pharmaceutical exports, is hiring for the role of Trainee – Business Development and Regulatory Affairs in Indore, Madhya Pradesh.

This is your chance to gain hands-on experience in international business development, regulatory compliance, and client coordination with one of India’s growing pharma companies.

Role & Responsibilities

1. As a Business Development & Regulatory Affairs Trainee, you will:

2. Assist in international marketing and pharmaceutical business development.

3. Support regulatory documentation, compliance, and submissions.

4. Coordinate with global clients and strengthen business relationships.

5. Learn industry best practices in export-focused pharmaceutical operations.

Qualifications

• Education: B.Pharm / M.Pharm / B.Sc / M.Sc

• Experience: 0–2 years (Freshers encouraged to apply)

• Skills: Strong communication, willingness to learn, interest in pharma exports & regulatory affairs.

Benefits

• Monthly stipend: ₹10,000 – ₹12,000

• Hands-on exposure to international pharma business.

• Growth opportunities in regulatory affairs and business development.

• Supportive and dynamic learning environment.

Drug Safety Associates

If you’re passionate about pharmacovigilance and want to build a rewarding career at the intersection of healthcare and technology, this is your chance. Indegene, a global leader in technology-led healthcare solutions, is hiring Drug Safety Associates (Pharmacovigilance Officer I) in Bangalore.

This role is perfect for fresh graduates and early-career professionals looking to work on drug safety monitoring, case processing, and regulatory compliance. At Indegene, you’ll not only gain hands-on experience in pharmacovigilance but also fast-track your career with world-class training and mentorship.

Key Responsibilities

As a Drug Safety Associate at Indegene, you will:

1. Validate safety cases and confirm minimum criteria for case creation.

2. Perform duplicate searches and process initial/follow-up cases.

3. Handle patient safety case processing in line with global regulatory requirements.

4. Identify serious adverse events (SAEs)and special case scenarios (lack of efficacy, pregnancy exposure, product quality issues).

5. Attach and review relevant source documents for case submissions.

6. Perform medical coding for adverse events, medical history, lab data, and indications using MedDRA.

7. Code products (suspect, co-suspect, concomitant) per client and regulatory guidelines.

8. Draft clear and accurate safety narratives.

Desired Qualifications

To succeed in this role, you should have:

1. Knowledge of pharmacovigilance and the drug safety case-handling process.

2. Understanding of the overall drug development and research process.

3. Strong attention to detail, verbal reasoning, and analytical thinking.

4. Good command of medical terminology and therapy areas.

5. Excellent comprehension, communication (written & verbal), and interpersonal skills.

Nice-to-Have Skills

• Prior experience or training in clinical research / pharmacovigilance.

• Familiarity with regulatory reporting systems and safety databases.

Benefits of Joining Indegene

• Opportunity to work with a global healthcare leader.

• Career growth at the intersection of healthcare and technology.

• Mentorship from experienced professionals.

• Inclusive workplace with equal opportunity policies.

• Fast-track career development for freshers and early-career talent.

Clinical Data Management

Red Nucleus is a global strategic partner and advisory company for the life sciences industry, offering a comprehensive suite of services across the entire product lifecycle. They provide scientific and medical communications, market access support, and learning & development solutions. With a commitment to improving health outcomes, Red Nucleus acts as a “red thread” connecting diverse services to help pharmaceutical and biotech companies achieve transformative success.

Are you looking to grow your career in Clinical Data Management while working with global life sciences clients? Red Nucleus is hiring Associate / Senior Associate, Clinical Data Management (Remote – India). This is a client-facing role where you’ll manage innovative EDC and ePRO data solutions, interact with clients daily, and ensure compliance with international regulatory standards.

If you have strong communication skills, experience in clinical research data management, and are ready to work on cutting-edge projects, this opportunity is for you.

Key Responsibilities

1. Review, reconcile, transfer, and migrate clinical & ePRO data

2. Prepare critical documentation: Data Management Plans, Migration Plans, CRF specifications

3. Ensure timelines, quality, and compliance are met

4. Coordinate with multiple stakeholders including clients and vendors

5. Maintain compliance with GCP, ICH, HIPAA, GDPR, and FDA 21 CFR Part 11

 Qualifications

1. 0–10 years of experience in Clinical Data Management or Clinical Research

2. Strong verbal & written communication skills (client-facing experience is a plus)

3. Knowledge of clinical regulations: GCP, ICH, HIPAA, GDPR, FDA 21 CFR Part 11

4. Ability to simplify complex processes and deliver documentation with precision

5. Immediate joiners or candidates available within 30 days preferred

Benefits of Joining Red Nucleus

• 100% Remote opportunity in India

• Exposure to global clinical trials and patient-reported data projects

• Work on advanced ePRO & EDC platforms like iTakeControl

• Collaborate with international teams and clients

• Competitive salary & growth opportunities

How to Apply

Interested candidates can apply by sending their updated resume to:

📧 ssingh@rednucleus.com

NIeCer 102: Ethics Review of Health Research

ICMR-National Institute of Epidemiology (NIE) offers NIE-ICMR-WHO online course  NIeCer 102: Ethics Review of Health Research. The course is technically supported by the World Health Organization (WHO), India. The course will provide the fundamentals of ethical issues in biomedical research involving human participants and provide updates on research ethics guidelines in India.

This is a self-aced course. The participants can go through the learning materials and submit the self-assessment quiz at any-time after the enrolment into the course.

INTENDED AUDIENCE : This course is intended for members of India's institutional ethics committees and institutional review boards (including secretarial staff) and professionals engaged in biomedical research involving human participants [any current or potential health researchers (clinical/public health /laboratory researchers, physicians, research associates, allied health professionals, scientists, statisticians, research administrators / managers)]

Summary

• Course Status : Running

• Course Type : Elective

• Language for course content : English

• Duration : Self Paced

• Category : Multidisciplinary

• Level : Certificate

COURSE CONTENT 

GENERAL ETHICAL PRINCIPLES

1.  Introduction to health research ethics

2.  International guidelines on ethical conduct of health research

3.  National ethical guidelines for biomedical and health research involving human participants

4.  National ethical guidelines for biomedical research involving children - An overview

5.  Benefits and risks in health research - principles, types and categories

RESPONSIBLE CONDUCT OF RESEARCH

6.  Responsibilities of a researcher

7.  Rights and duties of researchers, sponsors, participants, and IEC members under the Indian Constitution

8.  Collaborative research 

9.  Academic/investigator initiated clinical trials

10. Regulations and guidelines for conduct of clinical trials in India

11. Good clinical practices and clinical trial registry of India 

FUNCTIONING OF ETHICS COMMITTEES

12. Establishment of ethics committees 

13. Administration of research ethics committees 

14. Roles and responsibilities of ethics committee members 

15. Monitoring ongoing research by ethics committees 

REVIEW OF RESEARCH PROPOSALS 

16. Conduct of research ethics committee review meeting 

17. Conflicts of interest  

18. Rationale and science of the research proposal

19. Risk benefit assessment process

PROTECTION OF RESEARCH PARTICIPANTS

20. Protection of privacy and confidentiality of research participants 

21. Critical importance of informed consent in health research 

22. Informed consent process 

23. Informed consent in special situations 

24. Payments-Incentives, compensation and reimbursement

25. Vulnerable populations in health research 

26. Research during humanitarian emergencies and disasters 

This course has been developed and delivered by eminent professionals and researchers from cross-cutting domains who are involved in various organizations and committees in India related to biomedical ethics.

COURSE COORDINATOR  

Prof (Dr) S Lokesh M.D (Gen Med), FIRD, FIMSA

TEACHING ASSISTANTS 

R. Ramakrishna Rao, M.com, M.Sc, M.A

R. Vijayaprabha, MSW

TECHNICAL ASSISTANT 

M. Saravanan, M.Sc

Course certificate

e-certificate will be awarded to the successful course participants based on the score of ≥50% in each assignment.

Medical Writing – Remote

Location Options: Remote across the UK, Belgium, Czech Republic, Hungary, Spain (Madrid), and 7+ more countries

Job Type: Full-Time

Company: Syneos Health®

About Syneos Health

Syneos Health® is a leading global biopharmaceutical solutions company with 29,000+ employees across 110 countries. We partner with top pharmaceutical, biotech, and medical device organizations to accelerate clinical development, medical affairs, and commercial success.

At Syneos Health, work here matters everywhere. We are committed to innovation, collaboration, and creating therapies that change lives.

Why Join Us?

• Career growth and professional development opportunities

• Supportive leadership and ongoing training programs

• Recognition and rewards for your contributions

• A diverse and inclusive culture where you can be your authentic self

Role Overview – Manager, Medical Writing

We are seeking an experienced Manager, Medical Writing to lead and support our global medical writing team. This role involves managing staff, ensuring high-quality deliverables, and collaborating with cross-functional teams on clinical and regulatory documentation.

Key Responsibilities

• Lead and mentor medical writing staff, including performance reviews, training, and career development

• Review and edit medical writing deliverables for quality, accuracy, and compliance with sponsor requirements

• Support strategy development for document creation and quarterly business updates

• Contribute to project budgeting, revenue forecasting, and proposal development

• Represent medical writing in bid defenses, customer meetings, and business development activities

• Maintain departmental SOPs, templates, and best practices

• Oversee cross-functional project teams and resolve issues proactively

• Participate directly in writing and reviewing key clinical and regulatory documents when needed

• Ensure compliance with FDA, EMA, ICH, and ISO guidelines

• Travel up to 25% may be required

Qualifications

• Bachelor’s degree in life sciences, pharmacy, or related field (advanced degree preferred)

• Strong background in medical writing within CRO, pharmaceutical, or medical device companies

• Previous leadership or management experience strongly preferred

• Deep knowledge of clinical research regulations (FDA, EMA, ICH, ISO)

• Excellent written and verbal communication skills in English

• Strong organizational, leadership, and interpersonal skills

• Proficiency in Microsoft Office Suite

About Our Work

Over the past 5 years, Syneos Health has supported:

1. 94% of all FDA-approved novel drugs

2. 95% of EMA-authorized products

3. 200+ clinical studies across 73,000 sites and 675,000+ trial patients

When you join us, you’ll be part of a team that pushes boundaries, embraces challenges, and delivers results that matter.

👉 Learn more about Syneos Health at www.syneoshealth.com (http://www.syneoshealth.com/)

Are you looking to grow your career in clinical research? Microdata Labs is hiring Clinical Research Coordinators (CRC) for its clinical trial operations in Indore and Patna. This is a great opportunity for life sciences and pharmacy graduates to work on diverse clinical studies, gain hands-on experience, and contribute to advancing healthcare.

With 2 open positions (1 in Indore and 1 in Patna), the company is seeking skilled and motivated professionals who can ensure high-quality trial execution while maintaining regulatory compliance.

Last Date to Apply: Monday, 25th August, 2:00 PM

Location: Indore (1), Patna (1)

Joining: Immediate

Key Responsibilities

As a Clinical Research Coordinator, you will:

1. Coordinate and manage daily clinical trial operations.

2. Facilitate subject recruitment, screening, enrollment, and follow-up.

3. Maintain accurate and complete study documentation as per ICH-GCP guidelines.

4. Act as a liaison between investigators, sponsors, monitors, and internal teams.

5. Ensure compliance with study protocols, GCP, and applicable regulations.

Required Qualifications

1. Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or related field.

2. Prior experience as a CRC or in clinical research is an advantage.

3. Strong communication, organizational, and interpersonal skills.

4. Ability to manage responsibilities independently and efficiently.

Why Join Microdata Labs?

Work on diverse clinical studies across multiple therapeutic areas.

Be part of a collaborative, growth-driven, and supportive team.

Competitive remuneration and career advancement opportunities.

Application Process

Interested candidates should send their updated CV to:

careers@microdatalabs.com

Use the subject line:

“Application for CRC – [Indore/Patna]”

Applications submitted after Monday, 25th August, 2:00 PM will not be considered.

Pharmacovigilance Services Associate 

Position: Pharmacovigilance Services Associate

Job Type: Full-time

Experience: 0–3 Years (Freshers can apply)

Job ID: AIOC-S01565831

Location: Bengaluru, India

About Accenture

Accenture is a global professional services leader, known for driving innovation and delivering transformative business solutions. With expertise spanning digital, cloud, security, strategy, consulting, and operations, Accenture partners with the world’s most successful organizations to reimagine their future.

With 699,000 professionals serving clients in more than 120 countries, Accenture combines advanced technology with human ingenuity to create long-term value. The company is deeply committed to empowering people, communities, and industries with meaningful solutions that make a global impact.

Role Overview

Accenture is seeking passionate and detail-oriented individuals to join its Life Sciences R&D vertical as Pharmacovigilance Services Associates.

This role is ideal for fresh graduates or early professionals looking to begin a career in drug safety and regulatory compliance. You will be part of a dedicated team that helps global pharmaceutical leaders deliver safer and more effective healthcare solutions.

Key Responsibilities

As a Pharmacovigilance Services Associate, your day-to-day responsibilities will include:

1. Managing case identification, data entry, MedDRA coding

2. Handling affiliate mailbox management and report reconciliation.

3. Executing written follow-ups for both serious and non-serious cases.

4. Ensuring all processes comply with global regulatory requirements and client-specific guidelines.

5. Collaborating within a team environment and supporting projects with a patient-centric approach.

6. Working in rotational shifts as required to support global operations.

What Accenture is Looking For

Accenture values professionals who are eager to learn and grow in a fast-paced environment. The ideal candidate should have:

• Agility for quick learning and adapting to new processes.

• Flexibility to manage different types of tasks.

• Strong teamwork and collaboration skills.

• A detail-oriented approach and commitment to maintaining quality.

Qualifications

Educational Requirement: B.Sc / Bachelor of Pharmacy (https://pharmajobspost.in/lupin-receives-tentative-approval-from-u-s-fda-for-obeticholic-acid-tablets/) / Bachelor of Physiotherapy

Experience: 0–2 years (Fresh graduates and candidates with up to 2 years of experience are encouraged to apply)

Why Join Accenture?

By joining Accenture, you will:

• Gain exposure to global pharmaceutical projects and leading biopharma clients.

• Work in a domain that directly contributes to patient safety and regulatory excellence.

• Build a solid foundation in Pharmacovigilance & Drug Safety Surveillance.

• Explore multiple career growth opportunities within Life Sciences R&D.