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Clinical Research Associate

• Gurugram ,India
• Posted 6 days ago

Website Nirvasa Healthcare

Transforming the Digital Healthcare Landscape in India

Job description

Degree Requirement:  Bachelor of Pharmacy (B Pharma) or Diploma in Pharmacy (D-Pharma) with at least 6 months of relevant experience.

Job Description:  We are seeking a dedicated and detail-oriented Clinical Research Associate to join our dynamic team. The ideal candidate will possess a solid understanding of medical terms, pathophysiology of illnesses, drug knowledge as per the medical condition, excellent organizational skills, and the ability to work effectively in a fast-paced environment. As a Clinical Research Associate, you will play a vital role in assisting the formulation and implementation of healthcare programs aimed at improving clinical assessments.

Responsibilities:

• Clinical Assessment Formulation:  Collaborate with cross-functional teams to develop and refine clinical assessment protocols and methodologies. Conduct literature reviews and stay abreast of emerging trends in clinical research to inform assessment  strategies.
• Healthcare Program Development:  Assist in the design, planning, and execution of healthcare programs aimed at improving patient outcomes. This includes contributing to the development of study protocols, case report forms, and other study-related documents.
• Data Collection and Analysis:  Oversee the collection, management, and analysis of clinical data to ensure accuracy and compliance with regulatory standards. Perform statistical analysis and interpret findings to support decision-making processes.
• Content Creation:  Research, write, and edit medical content for various platforms, including websites, blogs, social media, and marketing materials. Develop content that is accurate, well-researched, and aligned with client objectives and target audience needs.

Qualifications:

• Bachelor of Pharmacy (B Pharma) or Diploma in Pharmacy (D-Pharma) from a recognized institution.
• Minimum of 6 months of experience in clinical research/ medical writing or a related field.
• Proven experience in medical writing, healthcare communications, or a related field. Previous experience in pharmaceutical or medical device industries is desirable.
• Excellent writing and editing skills, with the ability to convey complex medical information in a clear, concise, and engaging manner.
• Familiarity with medical terminology, anatomy, physiology, pharmacology, and disease mechanisms.
• Detail-oriented with a commitment to accuracy, quality, and compliance.
• Ability to work independently, manage multiple projects simultaneously, and meet deadlines in a fast-paced environment.
• Strong communication and interpersonal skills, with the ability to collaborate effectively with diverse stakeholders.

To apply for this job please visit www.naukri.com .

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surbhi | 11 April, 2024 | 8:46 AM IST

Thermo Fisher Hiring Freshers In Clinical Research As Safety Reporting Coordinator – Multiple Locations Apply Now

Thermo Fisher Scientific

Experience :

0 Years / Freshers - 2 Years

₹4.4 Lakhs [ ₹3.5 L/yr - ₹7.9 L/yr]

Mumbai, Hyderabad, Haryana, Bangalore

At Thermo Fisher Scientific, we're committed to meaningful work that has a global impact. Join us in bringing our Mission to life - empowering our customers to create a healthier, cleaner, and safer world. Our Clinical Research team, which drives our PPD® clinical research portfolio, is part of our leading global contract research organization (CRO). We offer our teams the resources they need to achieve individual career goals while advancing science through research, development, and delivery of life-changing therapies.

Safety Reporting Coordinator

Department :

Clinical Trials, Clinical Research

Education :

B.Pharm, M.Pharm, M.Sc, B.Sc, Pharm.D

Job Lcation :

Job Description

• Provide administrative support to the safety reporting team and Pharmacovigilance department.
• Handle tasks related to receipt and submission of expedited and periodic safety reports, ensuring compliance with regulatory timelines and legislation.
• Assist in producing project metrics and alert managers to any quality or timeline issues.
• Maintain safety reporting systems and information in a timely manner.
• Liaise with various departments and external parties regarding safety reporting tasks and project setup.
• Troubleshoot daily operational issues independently.
• Train Pharmacovigilance department staff on safety reporting processes and associated systems.
• Assist with audit and inspection preparation if required.
• Perform against Key Performance Indicators (KPIs) for projects.

Requirements:

• Relevant formal academic or vocational qualification.
• 0 to 2 years of comparable previous experience.
• Proficiency in Microsoft Office Programs (Word, Excel, PowerPoint).
• Good knowledge of Pharmacovigilance and industry terminology.
• Strong written and verbal communication skills.
• Ability to prioritize tasks and handle numerous deadlines effectively.
• Strong attention to detail and organizational skills.
• Ability to work effectively in a team and independently.

Mission Statement:

Our Mission is to enable our customers to make the world healthier, cleaner, and safer. As part of Thermo Fisher Scientific, we value diverse experiences, backgrounds, and perspectives, working together to accelerate research, solve complex scientific challenges, drive technological innovation, and support patients in need.

Apply Today: Thermo Fisher Scientific Careers

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other legally protected status.

Most Popular Jobs

Searching for a fulfilling position at Thermo Fisher Scientific? We are looking for a qualified applicant for Safety Reporting Coordinator in our Clinical Trials, Clinical Research team right now. The ideal applicant will have 0 Years / Freshers - 2 Years years of relevant experience, at least, and B.Pharm, M.Pharm, M.Sc, B.Sc, Pharm.D. With its headquarters in Mumbai, Hyderabad, Haryana, Bangalore, this role pays a competitive Salary. We encourage you to apply if you have a strong interest in Department-related field and are prepared to make a difference. Come work with us at Thermo Fisher Scientific and become a member of our committed team that promotes quality and innovation in Clinical Trials, Clinical Research.

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