ICON plc Hiring a Pharmacovigilance Reporting Associate – Safeguard Patient Safety

Overview

ICON plc, one of the world’s leading Clinical Research Organizations (CROs), is actively hiring Pharmacovigilance Reporting Associates. This role is essential for ensuring drug safety, regulatory compliance, and patient protection across clinical trials and post-marketing surveillance.

For candidates aiming to establish themselves in pharmacovigilance jobs India, drug safety associate Bulgaria, or global PV careers, this is a golden opportunity.

Key Responsibilities

• Preparing & reviewing safety reports including Periodic Safety Update Reports (PSURs) and Individual Case Safety Reports (ICSRs)

• Collecting and analyzing adverse event data from both clinical trials and post-marketing surveillance

• Using industry-standard coding systems like MedDRA, ICD-10, and WHO-DD

• Collaborating with regulatory authorities, sponsors, and cross-functional teams

• Ensuring compliance with ICH guidelines, Good Pharmacovigilance Practices (GVP), and local regulations

Candidate Profile

• Education: Bachelor’s in Life Sciences, Pharmacy, or related field (B.Pharm, M.Sc, PharmD)

• Experience: 0–3 years in pharmacovigilance or drug safety (Freshers with PV knowledge welcome)

• Skills: Strong communication, attention to detail, and ability to work with Argus, SafetyEasy, and PV tools

• Preferred: Prior experience with ICSR triage, narrative writing, and global case submissions

Salary & Benefits

• Average salary: ₹5–8 LPA in India (higher for global roles like Bulgaria/EU)

• Health Insurance for family

• PF/Retirement contributions

• Flexible leave policies, professional development training, and career growth opportunities

Application Process

• Visit ICON plc Careers

• Search for Job ID: JR134477

• Apply with updated CV, cover letter, and PV experience details

• Direct link: Apply Now – ICON Pharmacovigilance Reporting Associate

Fortrea Hiring Clinical Pharmacist – Early Phase Trials

Overview

Fortrea, a global clinical research leader, is hiring Clinical Pharmacists in Daytona Beach, Florida. This office-based role supports Phase I clinical trials, ensuring the safety, compliance, and effectiveness of investigational drugs.

For those searching clinical pharmacist jobs Florida or pharma CRO careers Daytona Beach, this role provides stability, growth, and excellent compensation.

Responsibilities

• Develop and review study protocols, pharmacy manuals, preparation logs

• Ensure sterile compounding and adherence to pharmacy regulations

• Work with sponsors and regulatory bodies to demonstrate compliance

• Conduct feasibility checks for clinical trial projects

• Provide technical pharmaceutical guidance to clinical teams

Candidate Profile

• Registered Pharmacist / PharmD (Florida license required)

• 2+ years of pharmacy experience in sterile compounding

• Preferred: Experience in hospital, long-term care, or research settings

• Ability to thrive in a protocol-driven, regulated CRO environment

Salary & Benefits

• Salary: $113,800 – $135,800 annually

• Medical, Dental, Vision, and Life Insurance

• 401(k) retirement plan

• Paid Time Off (PTO), employee recognition awards

• Growth opportunities in clinical research & CRO industry

Application Process

• Visit Fortrea Careers

• Job ID: 252820 – Clinical Pharmacist, Daytona Beach

• Direct link: Apply Now – Clinical Pharmacist Fortrea

EVERSANA Hiring Expert Writer – Medical Content Development

Overview

EVERSANA, a global leader in medical information, pharmacovigilance, and compliance solutions, is hiring Expert Writers in Medical Content Development. This remote role is ideal for professionals passionate about medical communications, scientific writing, and compliance-driven content creation.

Responsibilities

• Develop scientifically accurate response documents, FAQs, posters, abstracts, and training content

• Ensure compliance with MLR (Medical, Legal, Regulatory) review standards

• Use platforms like Veeva PromoMats and MedComms

• Conduct literature reviews using PubMed, Embase, and Ovid

• Mentor junior medical writers and contribute to SOP development

Candidate Profile

• Education: PharmD, PhD, MD, M.Pharm, or related degree

• Experience: 4+ years in medical writing, content development, or regulatory affairs

• Skills: Strong knowledge of AMA Style Guide, ICMJE, CONSORT, PRISMA, STROBE

• Traits: Collaborative, detail-oriented, and adaptable across multiple therapeutic areas

Benefits

• Remote-first model (global flexibility)

• Competitive compensation

• Diversity-friendly culture (rated 4.0/5 for inclusivity)

• Professional growth through global pharma projects

Application Process

• Visit EVERSANA Careers

• Apply for Medical Content Development – Expert Writer role

• Submit resume and cover letter showcasing writing experience

Navitas Life Sciences Hiring Study Nurse – Entry Level

Overview

Navitas Life Sciences is hiring Study Nurses in Manipal, Karnataka. This entry-level role in clinical research nursing is perfect for freshers (ANM/GNM/B.Sc Nursing) who want to start their career in pharma and CROs.

High CPC search terms like clinical research nurse jobs Manipal and entry-level pharma nursing careers align with this role.

Responsibilities

• Perform vital checks, CRF documentation, blood collection, IV cannulations

• Manage emergency medicine stocks and study-related supplies

• Monitor ICU/BA/BE wards during trials

• Ensure regulatory and SOP compliance in clinical study execution

• Handle volunteer management, screening, BMI checks

Candidate Profile

• Qualification: ANM, GNM, or B.Sc Nursing with registration

• Experience: 0–2 years (freshers welcome)

• Skills: Compassion, accuracy, attention to detail, computer literacy

• Shift flexibility required

Benefits

• Stable career entry into clinical research

• Mentorship and professional development

• Exposure to ICU, ward management, and trial monitoring

Application Process

• Apply via Navitas Careers

• Upload resume, certificates, and cover letter

Aragen Life Sciences Hiring Junior Research Associate – Freshers

Overview

Aragen Life Sciences is offering Junior Research Associate roles in Synthesis R&D, ideal for M.Sc Organic Chemistry freshers (2025 batch). This is one of the top opportunities for students searching freshers pharma jobs in India or junior research associate organic chemistry careers.

Responsibilities

• Execute chemical reactions for synthesis of drug molecules

• Document experiments and maintain lab safety standards

• Collaborate with senior scientists in drug discovery projects

• Support analytical evaluation and optimization of synthetic routes

Candidate Profile

• Education: M.Sc Organic Chemistry (2025 batch only)

• Experience: 0–6 months

• Skills: Strong organic chemistry knowledge, eagerness to learn lab techniques

• Traits: Safety-first mindset, detail-oriented, and collaborative

Hiring Process

• Technical Test (Organic Chemistry concepts)

• Technical Interview with R&D team

• HR Round – career alignment and culture fit

Application Process

• Visit Aragen Careers

• Apply for Junior Research Associate – Synthesis R&D.