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Remote Hiring At Kelly Science

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Remote Hiring At Kelly Science

Remote Hiring At Kelly Science

Position Overview
Kelly Science and Clinical is hiring an Associate Essential Document Specialist to support clinical trial documentation management. Known for connecting talent with leading scientific opportunities, Kelly offers a chance to advance your career in clinical research while working from home. This role focuses on ensuring the quality, integrity, and compliance of essential clinical trial documents, offering a rewarding environment for professionals looking to make an impact in life sciences. Remote Hiring At Kelly Science

Position Details

PositionAssociate Essential Document Specialist
LocationRemote (Work from Home)
Experience LevelMinimum 1 year
SalaryNot Disclosed
Educational RequirementsB.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Life Sciences
Application TypeOnline Application
Verified PositionYes

Job Highlights

  • Work/Life Balance: Flexible remote role supporting clinical trial documentation.
  • Growth Opportunity: Build expertise in essential document management within clinical research.
  • Collaborative Environment: Work closely with internal teams and external partners. Remote Hiring At Kelly Science

About the Role

As an Associate Essential Document Specialist, you will contribute to the successful management of essential clinical trial documents, focusing on compliance and regulatory standards. Working under the guidance of Essential Document Specialists and Leads, this role requires strong organizational skills and a keen eye for detail. Remote Hiring At Kelly Science

Key Responsibilities

  • Document Support: Assist in managing clinical trial documentation to ensure records are accurate and compliant.
  • Process Optimization: Develop strategies and tools to streamline documentation, adhering to regulatory standards.
  • Document Integrity: Oversee the integrity and readiness of clinical trial documents, ensuring timely processing.
  • Trial Master File Management: Create and maintain Trial Master File (TMF) Plans, assist with archival, and review TMF content.
  • Communication: Liaise with clinical teams and external partners, ensuring effective document management.
  • Reporting: Provide regular updates on TMF status and support audit and inspection readiness.
    Remote Hiring At Kelly Science
Remote Hiring At Kelly Science
Remote Hiring At Kelly Science

Required Qualifications

RequirementsDetails
EducationMinimum high school diploma; Bachelor’s in a relevant field preferred
ExperienceAt least 1 year in clinical research or a related role
Regulatory KnowledgeGeneral knowledge of ICH-GCP guidelines and relevant regulations
Clinical KnowledgeFamiliarity with clinical development and trial management systems
Remote Hiring At Kelly Science

Skills Required

  • Attention to Detail: High precision in document handling to maintain integrity.
  • Time Management: Ability to manage tasks efficiently and meet deadlines.
  • Technical Proficiency: Skills in Adobe Acrobat and Microsoft Office Suite (Word, Excel, Outlook).
  • eTMF Knowledge: Familiarity with electronic Trial Master Files (eTMF) is a plus.
  • Communication Skills: Strong verbal and written communication for effective collaboration.
    Remote Hiring At Kelly Science

Why Join Kelly Science and Clinical?
Kelly has a legacy of bridging the gap between top talent and groundbreaking opportunities in the life sciences sector. As an Associate Essential Document Specialist, you’ll have the chance to develop your expertise in clinical documentation, work with dynamic teams, and play a vital role in supporting clinical trials
Remote Hiring At Kelly Science.

Working Hours
This is a flexible, remote role with standard working hours designed to support work/life balance.

How to Apply:
Submit your application through the Kelly Science and Clinical career portal. This verified position is open to candidates with at least one year of clinical research experience, a strong foundation in regulatory requirements, and an interest in growing within clinical trial management.
Remote Hiring At Kelly Science

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Start your journey in clinical documentation with Kelly Science and Clinical – Apply today!

Meta Description:
Associate Essential Document Specialist at Kelly Science and Clinical – Work from home. 1 year of experience in clinical research required. Remote Hiring At Kelly Science

Remote Hiring At Kelly Science
Remote Hiring At Kelly Science

Academically Hiring for Online Pharmacy Lecturer

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Academically Hiring for Online Pharmacy Lecturer

Academically Hiring for Online Pharmacy Lecturer

PositionOnline Pharmacy Lecturer
CompanyAcademically
Experience1 – 5 Years
Salary₹20k – ₹1 Lakh Per Month
LocationWork from Home
EducationM.Pharm, Ph.D.
Key SkillsOnline Teaching, Pharmacy, Licensing Exam Prep
Application ProcessApply Online on Academically’s portal
Academically Hiring for Online Pharmacy Lecturer

Revolutionize Healthcare Education with Academically

Are you passionate about pharmacy education and looking for an opportunity to make a global impact from the comfort of your home? Academically is on a mission to transform the way aspiring pharmacists prepare for their careers through innovative, technology-driven learning solutions. As an Online Pharmacy Lecturer, you will play a crucial role in helping students around the world succeed in global pharmacy licensing exams in countries like Australia, the USA, Ireland, Gulf nations, and competitive Indian exams such as GPAT and NIPER. Academically Hiring for Online Pharmacy Lecturer

This part-time, work-from-home opportunity is ideal for educators who want to impart knowledge, guide students, and contribute to the development of future healthcare professionals. Academically Hiring for Online Pharmacy Lecturer

What You’ll Do as an Online Pharmacy Lecturer

In this role, you will be responsible for creating and delivering engaging, interactive online courses that prepare students for a range of pharmacy exams. Whether you’re conducting live online lectures, creating hands-on learning experiences, or mentoring students one-on-one, your work will directly influence the success of future pharmacists. Academically Hiring for Online Pharmacy Lecturer

Here’s a glimpse of your key responsibilities:

  • Develop and Deliver Courses: You’ll design and teach online courses focused on preparing students for international pharmacy licensing exams (e.g., USA, Australia, Gulf countries) and Indian competitive exams (GPAT, NIPER).
  • Interactive Learning: Craft interactive lectures and practical sessions to make complex pharmaceutical concepts easy to understand.
  • Assess Student Progress: Design assessments, assignments, and exams to evaluate students’ understanding and ensure they’re on track to excel.
  • Collaborate on Course Design: Work closely with fellow educators and instructional designers to continually improve the quality of your courses.
  • Mentor Students: Provide personalized mentorship, helping students stay motivated and achieve their educational goals.
    Academically Hiring for Online Pharmacy Lecturer
Academically Hiring for Online Pharmacy Lecturer
Academically Hiring for Online Pharmacy Lecturer

Why This Job is Perfect for You

If you’re passionate about both education and the pharmaceutical sciences, this job offers a unique opportunity to impact the future of healthcare on a global scale. Working remotely offers a level of flexibility that allows you to balance work with your personal life, all while making a difference for students from diverse backgrounds.
Academically Hiring for Online Pharmacy Lecturer

Who We’re Looking For: Key Qualifications

  • Educational Background: You’ll need to hold an M.Pharm or Ph.D. in Pharmaceutical Chemistry, Pharmacology, or Pharmaceutics from esteemed institutions like NIPER, BHU, or Jamia Hamdard, or their equivalent.
  • Teaching Experience: 1-5 years of teaching experience is required, particularly in pharmacy exam preparation (GPAT, NIPER, or similar).
  • Licensing Exam Prep Expertise: Experience teaching students preparing for GPAT, NIPER, or international licensing exams is highly preferred.
  • Familiarity with E-Learning: Experience with online teaching platforms will be a huge plus.

Additional skills that will make you stand out:

  • Excellent Communication Skills: You should be able to communicate clearly and effectively, both in writing and verbally.
  • Engagement and Motivation: An ability to engage students from diverse backgrounds and keep them motivated is key.
  • Passion for Inclusive Education: We’re looking for someone who is dedicated to creating an inclusive learning environment for all students.
    Academically Hiring for Online Pharmacy Lecturer
Academically Hiring for Online Pharmacy Lecturer
Academically Hiring for Online Pharmacy Lecturer

Why Work at Academically?

Academically is more than just an educational platform—it’s a community dedicated to innovation and excellence in healthcare education. Here’s why you should join us:

  • Work from Anywhere: Enjoy the flexibility of working from home, allowing you to balance professional and personal commitments while making a global impact.
  • Professional Growth: Collaborate with other academic professionals and refine your teaching techniques with the latest technological tools.
  • Innovative Environment: Be part of a forward-thinking team that is revolutionizing pharmacy education through technology.
    Academically Hiring for Online Pharmacy Lecturer

How to Apply

Ready to join us in shaping the next generation of healthcare professionals? Apply online through Academically’s portal, and become part of a dynamic team that’s leading the way in pharmacy education. We look forward to hearing from you!

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Fresher CI Scientists Hiring for Analyst Role

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Fresher CI Scientists Hiring for Analyst Role

Fresher CI Scientists Hiring for Analyst Role

CI Scientists, a pioneer in clinical research, data management, and healthcare intelligence, is looking for talented freshers to join its innovative team. Our focus is on supporting oncology research with advanced data solutions, and we’re offering a unique work-from-home opportunity that allows you to start your career in a flexible, supportive environment. Fresher CI Scientists Hiring for Analyst Role

Job at a Glance:

PositionAnalyst
Salary20-28k per month
Mode of WorkWork-from-Home
QualificationsPh.D., M.Pharm, M.Sc
DepartmentOncology Database Intelligence
Job HighlightsWork/Life Balance, Flexibility, Problem Solving

Why Join CI Scientists?

At CI Scientists, we believe in unlocking the potential of fresh minds. Our focus on cutting-edge oncology research makes this an exciting place to apply your academic knowledge to real-world challenges. Whether you’re coming from a Ph.D., M.Pharm, or M.Sc. background, this Analyst role provides a perfect launchpad into the dynamic world of clinical data management and healthcare research. Fresher CI Scientists Hiring for Analyst Role

We’re proud to offer a remote work setup that supports flexibility and work-life balance, ensuring that you can thrive both personally and professionally. At CI Scientists, we foster a collaborative environment that nurtures innovation, making it easier for new talent to make an immediate impact. Fresher CI Scientists Hiring for Analyst Role

Key Responsibilities

As an Analyst on our Oncology Database Intelligence Team, you’ll play a crucial role in driving our mission forward. Here’s what you’ll be doing:

  • Collaborate with the oncology research team to analyze and manage clinical data.
  • Support ongoing research projects by compiling and evaluating critical datasets.
  • Contribute meaningful insights that aid in oncology studies, helping advance cancer research.
  • Ensure accuracy and maintain the integrity of clinical datasets to uphold research quality.

This is more than just a data-crunching job. You’ll be part of a team that helps researchers across the world make breakthroughs in oncology, directly impacting patient outcomes. Fresher CI Scientists Hiring for Analyst Role

Skills We’re Looking For

To succeed in this role, you need to have a passion for data and healthcare. Some key skills you’ll need include:

  • Strong analytical and problem-solving abilities to interpret clinical data effectively.
  • Familiarity with clinical research processes is highly valuable.
  • Proficiency in data management tools such as Excel, SQL, or R is a plus (but not mandatory).
  • Excellent communication skills—you’ll be working closely with teams and translating data into actionable insights.
  • The ability to work independently and take ownership of your projects. This is a remote position, so being self-motivated is essential.
    Fresher CI Scientists Hiring for Analyst Role

Why This Role is Perfect for Freshers

If you’re a recent graduate eager to make an impact in healthcare research, this is the perfect opportunity. You’ll get to work on real-world oncology data, applying the skills you’ve learned during your studies. It’s a chance to gain hands-on experience in an industry that’s always in demand, while still enjoying the freedom and flexibility of a work-from-home role. Fresher CI Scientists Hiring for Analyst Role

How to Apply

Ready to kickstart your career? We want to hear from you! Send your resume to:
📧 hr@ciscientists.com

CI Scientists is dedicated to finding the best fresh talent, and we can’t wait to see how you can contribute to our mission in oncology research. If you’re passionate about data and want to work in a role where you can make a difference, apply now! Fresher CI Scientists Hiring for Analyst Role

Additional Reference

For more insight into the role, feel free to ask Tejswini, one of our current team members, on LinkedIn. She’s been thriving in the same role and can offer valuable guidance.

This role offers you the chance to make a real-world impact while enjoying a flexible work environment. Apply today and join a team that’s committed to advancing oncology research through data-driven insights!

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Software Developer Intern at TECHPLEMENT – Cutting-Edge Solutions, Hands-On Experience, Flexible Work

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Job Posting: Software Developer Intern at TECHPLEMENT

Job Information

Position Name: Software Developer Intern

Company Name: TECHPLEMENT

Department: Software Development and Services

Qualification: Bachelor’s degree in computer science, IT, or engineering; Professional certification

Experience: Not specified in the provided text

Job Location: Remote/Online (Work From Home)

E-Mail: Not specified in the provided text

Company Description:

TECHPLEMENT is a Software Development and Services Company driven by innovation, specializing in web development, DevOps, AWS solutions, and more.

Who Can Apply:

  • Bachelor’s degree in computer science, IT, or engineering
  • Interest in learning new tools and technologies
  • Professional certification
  • Graduation year: 2023-2026 Batch Only

Objectives of this Role:

  • Build client-focused web applications
  • Support full-stack development using agile methodologies
  • Oversee teams for high-quality delivery
  • Design, develop, test, and enhance software solutions
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Responsibilities:

ResponsibilityDetails
Participate in full software development lifecycleAnalysis, design, test, and delivery
Develop web applications using various languagesUtilize software engineering principles
Facilitate design and architecture discussionsCollaborate for solutions and code reviews

Required Skills and Qualifications:

  • Strong understanding of Computer Science and Back-End Web Development
  • Knowledge of software engineering principles and practices
  • Experience with web development frameworks and technologies
  • Ability to work independently and collaboratively
  • Excellent problem-solving and communication skills
  • Knowledge of database systems and full-stack web protocols

Preferred Skills and Qualifications:

  • Bachelor’s degree in computer science, IT, or engineering
  • Interest in learning new tools and technologies
  • Professional certification

Perks:

  • Internship Completion Certificate
  • Letter of Recommendation (LOR)
  • Live Project Experience
  • Pre-Placement Offer (PPO) for outstanding performance

Duration: 1 Month
Work Time: Flexible
Work Place Type: Remote/Online
Stipend: Unpaid
Incentives: Performance-based
About Company: TECHPLEMENT specializes in crafting cutting-edge solutions and services, empowering clients to thrive in the digital age.

Meta Description:
Join TECHPLEMENT as a Software Developer Intern. Gain hands-on experience, certifications, and potential for a full-time role. Apply now!

Apply Online
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(Work From Home) Medical Writer I at Icon Plc

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Job Posting: Medical Writer I at Icon Plc (Work From Home)

About ICON

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us fulfill our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values: Accountability & Delivery, Collaboration, Partnership, and Integrity. We aim to be the Clinical Research Organization that delivers excellence to our clients and patients at every touchpoint.

Position Details

  • Position Name: Medical Writer I
  • Organization: Icon Plc
  • Qualification: B.Pharm, M.Pharm, Pharm.D, MSc, BSc, Lifesciences
  • Experience: 2-3 years
  • Salary: 6.10 LPA
  • Location: Work From Home

Responsibilities

  • Document Authoring: Author and perform QC of patient narratives.
  • Project Collaboration: Work with internal study teams to clarify project requirements and obtain necessary information.
  • Progress Tracking: Track and record progress using financial tracking tools and project databases. Flag projects not on track to management and facilitate the Change Order process.
  • Meeting Participation: Attend project meetings via teleconference/Webex.
  • Document Writing: Write documents according to contractual obligations and timelines using client or ICON templates and style guides.
  • Review Incorporation: Incorporate review comments from internal and external reviewers.
  • Quality Control: Perform QC of documents written by other writers.
  • Status Reporting: Keep senior management informed of project status and any issues.
  • Utilization Target: Achieve individual utilization (billability) target.
  • Operational Assistance: Provide general operational assistance to the Medical Writing team.
  • Process Improvement: Actively participate in department initiatives and process improvements.

Skills & Experience Required

Essential:

  • Bachelor’s/master’s degree in pharmacy/life science or equivalent.
  • 2-3 years of experience as a narrative/clinical/regulatory medical writer.
  • Proficiency in MS Word, Excel, PowerPoint, Adobe Acrobat, and Outlook.
  • Excellent verbal and written English skills.
  • Excellent attention to detail.

Preferred:

  • Experience working on oncology narratives.
  • Experience working for a large CRO.
  • Familiarity with Veeva Vault, Salesforce, and Box.

Competencies:

  • Ability to exemplify and promote ICON’s ‘Own It’ culture and values.
  • Proactive and collaborative communication skills.
  • Ability to work in a fast-paced, results-driven environment.
  • Culturally aware and able to work comfortably within a global team.

How to Apply

Apply Online
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    [Work From Home] Product Life Hiring in Pharmacovigilance

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    Job Posting: Case Specialist at ProductLife Group (Work From Home)

    About ProductLife Group

    ProductLife Group offers comprehensive solutions for pharmaceutical companies looking to streamline their operations and maximize efficiency.

    Position Details

    • Position Name: Case Specialist
    • Organization: ProductLife Group
    • Location: Work From Home
    • Salary: ₹25,000 – ₹35,000/month
    • Experience: 1 – 2 years
    • Qualification: B.Pharm, M.Pharm, Pharm.D

    Job Responsibilities

    TaskDescription
    Quality ControlConduct quality control of vigilance cases.
    Medical EvaluationPerform medical evaluations and pre-analyze complex cases before data entry.
    Data EntryEnter data for PV cases.
    Medical ReviewConduct medical evaluation of PV cases.
    Apply Online

    Requirements

    RequirementDescription
    EducationPharmacist qualification.
    ExperienceExperience in pharmacovigilance (PV) and database management, particularly with Argus.
    LanguagesProficiency in English.
    Technical SkillsProficient in Microsoft Office, strong teamwork abilities, attention to detail, flexibility, process-oriented, and organizational skills.

    Application Process

    Interested candidates are encouraged to apply promptly.

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    [WFH + Freshers] Thermo Fisher Scientific Hiring in Clinical Research

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    Job Posting: Assistant CRA at Thermo Fisher Scientific (Work From Home)

    About Thermo Fisher Scientific

    Thermo Fisher Scientific is dedicated to meaningful work that makes a positive impact on a global scale. Our Clinical Research team, part of our leading global contract research organization (CRO), is at the forefront of developing drugs that address the world’s most challenging health concerns.

    Position Details

    • Position Name: Assistant CRA
    • Organization: Thermo Fisher Scientific
    • Location: Work From Home
    • Salary: 4.1 to 7.1 Lacs per annum
    • Experience: 0 – 2 years (Freshers welcome)
    • Qualification: B.Pharm, M.Pharm, Pharm.D, MSc, BSc, Lifesciences
    Apply Online

    Key Responsibilities

    TaskDescription
    Study & Site ManagementComplete study and site management activities as defined in the task matrix.
    TrainingComplete study-specific training and orient on CRG/study-specific systems.
    Site SupportProvide in-house support during pre-study assessments and perform limited site contact activities.
    Document ReviewVerify document collection, review EMR/EHR checklists, and update site information.
    Patient MaterialsReview patient-facing materials and translations.
    Vendor ManagementSupport the vendor qualification process and maintain vendor trackers.
    Logistics CoordinationCoordinate study/site supply management and support logistics for IM attendance.
    Data ReconciliationPerform reconciliation tasks such as CRF, query status, deviations, and safety reports.
    Administrative TasksComplete expense reports and timesheets in a timely manner.

    Education and Experience

    • Education: Bachelor’s degree or equivalent in relevant academic/vocational qualification.
    • Experience: 0 to 2 years in a related field.

    Skills and Abilities

    • Basic medical/therapeutic area knowledge and understanding of medical terminology.
    • Solid understanding of ICH GCP, applicable regulations, and CRG procedural documents.
    • Effective oral and written communication skills.
    • Strong interpersonal and customer service skills.
    • Excellent time management and attention to detail.
    • Ability to work independently and in a team.
    • Proficient in MS Office and able to learn and use appropriate software.
    • Strong critical thinking and problem-solving skills.
    • Excellent English language and grammar skills.
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    Thermo Fisher Scientific Hiring Safety Specialist in Pharmacovigilance (Work From Home)

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    Thermo Fisher Scientific Hiring Safety Specialist in Pharmacovigilance (Work From Home)

    About Company:
    Our clinical research services team is dedicated to developing cures for the world’s most challenging health concerns. As part of the PPD® clinical research portfolio within our global CRO, we lead in clinical research and drug development.

    Position Name:
    Safety Specialist III – Pharmacovigilance

    Organization:
    Thermo Fisher Scientific

    Qualifications:

    • B.Pharm, M.Pharm, Pharm.D, MSc, BSc, Lifesciences

    Experience:

    • 1 to 2 Years

    Salary:

    • ₹4.8 Lakhs to ₹6.5 Lakhs

    Location:

    • Work From Home

    Job Details:

    Job TitleSafety Specialist III – Pharmacovigilance
    Job IDR-01243764
    Job TypeFull-time
    CategoryClinical Research
    LocationRemote, India
    Apply Online

    Responsibilities:

    ResponsibilitiesDetails
    Pharmacovigilance ActivitiesPerform day-to-day PV tasks: collection, monitoring, assessment, evaluation, and tracking.
    CollaborationCollaborate with project team members, clients, investigators, adverse event reporters.
    LeadershipOperate in a lead capacity, develop procedural documents, mentor less experienced staff.
    AuditsPrepare for and attend audits as required.
    Regulatory UpdatesStay updated on regulations, practices, and proposals by reviewing relevant publications.
    Medical UnderstandingMaintain understanding of therapeutic areas and disease states.
    Quality ReviewReview cases for quality, consistency, and accuracy, including peer report reviews.
    Project CoordinationHandle project implementation, client presentations, and review metrics and budgets.
    Literature SurveillanceAssess and peer review literature for adverse events and safety information.
    Primary ContactServe as the main contact for literature projects of varying complexity.
    ComplianceEnsure tasks adhere to company policies and regulations.
    Departmental InitiativesParticipate in departmental initiatives and inspections.

    Skills and Competencies:

    • Strong analytical and problem-solving skills.
    • Excellent written and oral communication skills.
    • Proficiency with PV databases and IT applications.
    • Ability to work effectively in a remote, team-oriented environment.
    • Strong organizational and coordination skills.
    • Knowledge of therapeutic areas and disease states relevant to current projects.

    Qualifications:

    • Relevant Bachelor’s or advanced degree in life sciences, pharmacy, nursing, or a related field.
    • Thorough understanding of global pharmacovigilance regulations and guidelines.

    How to Apply:
    Click the “Apply Now” button to start your application process.

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    [Work From Home] Thermofisher Scientific Hiring Safety Specialist in Pharmacovigilance

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    Job Posting: Safety Specialist in Pharmacovigilance at Thermo Fisher Scientific

    About Us
    Thermo Fisher Scientific’s clinical research services team is dedicated to bringing cures to market. We provide top-tier scientific and clinical expertise to develop drugs that address the world’s most challenging health concerns. As part of our PPD® clinical research portfolio within our global contract research organization (CRO), we are at the forefront of clinical research and drug development.

    Position NameSafety Specialist in Pharmacovigilance
    OrganizationThermo Fisher Scientific
    QualificationB.Pharm, M.Pharm, Pharm.D, MSc, BSc, Lifesciences
    Experience1 to 2 Years
    Salary Range₹4.8 Lakhs to ₹6.5 Lakhs
    LocationWork From Home
    Join WhatsApp

    Job Details

    • Job Title: Safety Specialist III
    • Location: Remote, India
    • Job ID: R-01243764
    • Job Type: Full-time
    • Category: Clinical Research
    • Remote: Fully Remote

    Job Description
    The Safety Specialist III oversees daily pharmacovigilance (PV) activities in a highly regulated environment. Responsibilities include collection, monitoring, assessment, evaluation, research, and tracking of safety information. This role involves collaboration with project team members, client contacts, investigators, adverse event reporters, and third-party vendors. The Safety Specialist III operates independently and may participate in on-call duties to ensure 24-hour case intake coverage from investigative sites.

    Key Responsibilities

    • Pharmacovigilance Activities: Conduct day-to-day PV activities including collection, monitoring, assessment, evaluation, research, and tracking of safety information.
    • Collaboration: Work effectively with project team members, client contacts, investigators, adverse event reporters, and third-party vendors.
    • Leadership: Lead in developing program and departmental procedural documents. Mentor junior staff.
    • Audits: Prepare for and attend audits as required.
    • Regulatory Updates: Stay current with global pharmacovigilance regulations and guidelines.
    • Medical Understanding: Maintain understanding of relevant therapeutic areas and disease states.
    • Quality Review: Ensure case quality, consistency, and accuracy, including peer review.
    • Project Coordination: Coordinate routine project tasks and presentations.
    • Literature Surveillance: Review literature for adverse events and safety information.
    • Primary Contact: Serve as primary contact for various literature projects.
    • Compliance: Ensure tasks are compliant with company policies and regulations.
    • Departmental Initiatives: Participate in departmental initiatives.
    • Audits and Inspections: Prepare for and attend audits and inspections as needed.

    Qualifications

    • Education: Bachelor’s or advanced degree in life sciences, pharmacy, nursing, or related field.
    • Regulatory Knowledge: Thorough understanding of global pharmacovigilance regulations and guidelines.
    • Skills: Strong analytical, problem-solving, communication, and organizational skills. Proficiency in PV databases and relevant IT applications. Ability to work effectively in a remote, team-oriented environment.

    Application Process
    Interested candidates should share their resumes via email to momita.sharma@thermofisher.com.

    Meta Description (19 words)
    Join Thermo Fisher as a Safety Specialist in Pharmacovigilance, leveraging your expertise remotely to advance clinical research and drug development.

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    [Work From Home] Parexel Hiring Medical Writer

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    Parexel Hiring Medical Writer I (Work From Home)

    Company Overview:
    Parexel is a global leader in clinical research and regulatory consulting. By applying for this role, you acknowledge that your application process will commence and information will be processed per Parexel’s Privacy Notice and Terms of Use. All submitted information must be accurate.

    Position Name:
    Medical Writer I

    Organization:
    Parexel

    Qualifications:

    • University degree in Life Sciences/Health or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, etc.), B.Pharm, M.Pharm

    Experience:

    • 1 to 2 Years

    Salary:

    • ₹4 Lakhs to ₹7 Lakhs Per Year

    Location:

    • Work From Home
    Apply Online

    Job Responsibilities:

    ResponsibilitiesDetails
    Aggregate Reports ManagementPrepare/update/merge Risk Management Plans (RMPs), Company Core-RMPs (CC-RMPs), and other safety reports.
    Literature ReviewConduct critical appraisal and systematic review of literature for safety reports and RMPs.
    Line ListingsGenerate and resolve discrepancies in Line Listings for submissions.
    Compliance and Quality ChecksPerform compliance activities and distribute final reports to stakeholders.
    Clinical Study Report NarrativesPrepare clear and accurate narratives from Clinical Database and Safety Database outputs.
    Signal Detection and ManagementReview and analyze signals from various sources; manage the signal management process end-to-end.
    General ResponsibilitiesMaintain knowledge of safety profiles, labeling documents, guidelines, and international regulations.
    Training and MentoringParticipate in training sessions, audits, and inspections; mentor new recruits.

    Skills and Competencies:

    • Strong analytical and problem-solving skills.
    • Excellent interpersonal and communication skills.
    • Ability to work collaboratively in a team environment.
    • Strong organizational and prioritization skills.
    • Client-focused approach with attention to detail.
    • Fluency in written and spoken English.
    • Proficiency with computer applications, particularly MS Office.

    Knowledge and Experience:

    • Relevant experience in Regulatory/Pharmacovigilance or related field is desirable.
    • Good knowledge of medical terminologies.

    How to Apply:
    Click the “Apply Now” button to start your application.

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