Gurgaon

Mediception Hiring for Senior Medical Writer

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Mediception Hiring for Senior Medical Writer

Mediception Hiring for Senior Medical Writer

Mediception Hiring for Senior Medical Writer If you’re passionate about translating complex medical and scientific data into clear, impactful content, this is the role for you! MediCeption Science Pvt Ltd is actively seeking a Senior Medical Writer to join their dynamic team in Gurugram, Haryana. This is your chance to play a key role in medical communications, clinical trials, and regulatory documentation while growing your career in one of the most exciting fields of healthcare. Mediception Hiring for Senior Medical Writer

Position Overview:

  • Position: Senior Medical Writer
  • Organization: MediCeption Science Pvt Ltd
  • Location: Gurugram, Haryana, India
  • Experience: 2 – 3 years
  • Qualification: M.Pharm, MSc, Ph.D in Medical or related fields
  • Salary: ₹4 – 6.5 LPA

MediCeption is a specialized clinical trial support service provider known for its cutting-edge approach to medical communications and regulatory documentation. This full-time, on-site role offers the opportunity to work on scientific content creation, medico-marketing, and clinical research—making it ideal for individuals who have a strong foundation in medical writing and are looking to take their careers to the next level. Mediception Hiring for Senior Medical Writer

Key Responsibilities:

As a Senior Medical Writer at MediCeption, you’ll be involved in a range of responsibilities that are crucial to the company’s operations in medical writing and communications. Here’s what you can expect:

1. Medical Writing & Scientific Content Creation

You will be responsible for creating high-quality scientific content and medical communication materials that cater to the needs of healthcare professionals and clients. This includes:

  • Developing slide decks, medico-marketing collaterals, and other communication tools.
  • Analyzing and interpreting scientific data and patient data to create informative and accurate content.
  • Working on clinical trial documentation and regulatory submissions, ensuring all materials meet industry standards and regulations. Mediception Hiring for Senior Medical Writer

2. Collaborating Across Functions

You will work closely with cross-functional teams to ensure that projects are delivered on time and meet both scientific and regulatory standards. This collaboration may include:

  • Interfacing with clinical research teams, regulatory affairs, and marketing teams to align the scientific content with broader company goals.
  • Literature reviews and systematic searches to support ongoing research projects, ensuring that all materials are backed by accurate and up-to-date data.

3. Supporting Clinical Research

You’ll play an essential role in supporting clinical research projects by conducting systematic literature reviews and contributing to scientific discussions. This role is key in ensuring that clinical data is accurately communicated to relevant stakeholders, from healthcare professionals to regulatory bodies.

Qualifications:

To excel in this role, MediCeption is looking for candidates who have the following qualifications and skills:

  • A Master’s degree (M.Pharm, MSc) or Ph.D. in a scientific or medical field.
  • 2-3 years of industry experience in medical writing, particularly in clinical trials or regulatory documentation.
  • Expertise in conducting literature searches and systematic reviews to support research.
  • Strong proficiency in medical communications and scientific writing, with the ability to present complex data in a clear and engaging manner.
  • Excellent written and verbal communication skills that enable you to work effectively with cross-functional teams.
  • Ability to work both independently and as part of a team, thriving in a collaborative environment.
    Mediception Hiring for Senior Medical Writer

Why Join MediCeption Science?

MediCeption Science is at the forefront of innovation in medical writing and clinical trial support services. Here are just a few reasons why you should consider joining their team: Mediception Hiring for Senior Medical Writer

1. Innovation and Technology

MediCeption prides itself on integrating the latest technologies in clinical trials, regulatory documentation, and medico-marketing. As a Senior Medical Writer, you’ll have the chance to work with cutting-edge tools that streamline processes and improve the quality of healthcare communications. Mediception Hiring for Senior Medical Writer

2. Ethical and Transparent Culture

At MediCeption, the company culture is built on ethics and transparency. You’ll be part of an organization that values integrity and strives to create content that adheres to the highest standards of scientific accuracy and regulatory compliance.

3. Career Development

Working at MediCeption offers numerous opportunities for career growth. Whether you’re looking to deepen your expertise in medical writing or branch out into regulatory affairs or clinical research, the company provides a pathway for career development. Mediception Hiring for Senior Medical Writer

4. Cross-Functional Exposure

You’ll have the opportunity to collaborate with a range of professionals across different disciplines, giving you exposure to clinical trials, research teams, marketing, and regulatory affairs. This not only broadens your skill set but also makes your role more dynamic and fulfilling. Mediception Hiring for Senior Medical Writer

5. Work/Life Balance

MediCeption places a strong emphasis on work-life balance, offering flexibility in work schedules. This balance allows you to maintain personal well-being while excelling in your professional role.

How to Apply:

If this role excites you and you meet the qualifications, don’t miss the opportunity to be a part of MediCeption’s talented team. Here’s how to apply:

  1. Prepare your resume that highlights your relevant qualifications and industry experience.
  2. Send your resume to bhawana@mediception.com, mentioning “Application for Senior Medical Writer” in the subject line. Mediception Hiring for Senior Medical Writer

Why This Opportunity is Perfect for You:

  • If you have 2-3 years of medical writing experience and are looking to move into a senior role where your expertise will be valued and expanded, this position offers the perfect opportunity.
  • Whether you are focused on clinical trials, scientific communications, or regulatory documentation, this role gives you exposure to all facets of medical writing.
  • The chance to work in a collaborative and ethical environment, where your skills and contributions directly impact the company’s success and the healthcare industry.
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Takeda Hiring Clinical Research Associate

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Takeda Hiring Clinical Research Associate

Company Overview:
Takeda Pharmaceutical Co., Ltd. is a global biopharmaceutical company with a 240-year history. Headquartered in Osaka, Japan, Takeda is committed to improving health through medical innovation.

Position Name:
Clinical Trial Associate

Organization:
Takeda

Qualifications:

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

Experience:

  • 3 Years

Salary:

  • ₹45,000 – ₹55,000 / month

Location:

  • Gurgaon, Haryana

Job Description:

Objectives:

  • Manage the Clinical Trial Management System (CTMS) and electronic Trial Master File (eTMF).
  • Oversee the review, approval, and accuracy of eTMF documents.
  • Generate reports to measure completeness, accuracy, and timeliness of the eTMF.

Accountabilities:

ResponsibilitiesDetails
Develop study-specific eTMF plansCreate plans tailored to individual clinical studies.
Perform quality controlEnsure documents meet eTMF specifications, ICH-GCP guidelines, regulatory requirements, and SOPs.
Address eTMF-related questionsProvide support and best practice recommendations for system users.
Maintain Essential Document Lists (EDLs)Keep EDLs updated and monitor study-specific eTMF trends.
Assist with inspections and auditsSupport inspection and audit-related activities.
Stay updatedKeep informed about the TMF Reference Model, industry best practices, and regulatory requirements.
Support Clinical OperationsAssist in overseeing CROs and collaborate with study teams to configure CTMS according to study requirements.
Lead meetingsAddress trends, issues, and establish industry standards.
Improve CTMS functionalityContinuously assess and track issues for future enhancements or training needs.
Apply Online

Education, Behavioral Competencies, and Skills:

  • Minimum Bachelor’s degree in science/healthcare field.
  • 3+ years of clinical research and TMF experience at a biotech, pharmaceutical company, or CRO.
  • Experience with eTMF system software, preferably Veeva Vault CTMS & eTMF.
  • Good knowledge of GCP and local clinical trial regulations.
  • Strong organizational and problem-solving skills.
  • Superior communication, strategic, interpersonal, and negotiating skills.
  • Proven stable performance over the past 2-3 years.

Travel Requirements:

  • Domestic travel: 20-30%, including some weekends.
  • International travel: 10-20%.

Employment Type:

  • Full-time, Regular Employee

Location:

  • Gurgaon, Haryana, India

Application Process:
By clicking the “Apply” button, you acknowledge that the employment application process with Takeda will commence. The information you provide in your application will be processed in line with Takeda’s Privacy Notice and Terms of Use. All information submitted in your application must be true to the best of your knowledge.

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J&J Hiring in Regulatory Affairs

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J&J Hiring in Regulatory Affairs
J&J Hiring in Regulatory Affairs


Location: Gurgaon, Haryana, India
Salary: Rs. 38,000 per month
Experience: 2-6 years

Company Overview:
Johnson & Johnson is a renowned American multinational specializing in pharmaceuticals and medical technologies, traded publicly on the NYSE.

Position Overview:
As a Sr. Executive in Regulatory Affairs, you will play a crucial role in ensuring regulatory and quality compliance across Johnson & Johnson’s medical franchises in India. This includes managing product life cycles, developing regulatory strategies, and coordinating with internal stakeholders for successful submissions to regulatory authorities.

Job Description

  1. Position Name: Sr. Executive, Regulatory Affairs
  2. Company Name: Johnson & Johnson
  3. Department: Regulatory Affairs
  4. Qualification: Graduate/Postgraduate in Lifescience/Biomedical/Pharmacy
  5. Experience: Minimum 2-6 years of industry experience in regulatory affairs, preferably in medical devices
  6. Job Location: Gurgaon, Haryana, India

Job Responsibilities:

  • Draft, review, and submit regulatory filings (e.g., re-registrations, new registrations, manufacturer transfers) for the Indian market.
  • Prepare and submit other regulatory submissions such as query responses, corrections filings, and post-registration lifecycle management notifications, adhering to regulations and guidelines.
  • Update and maintain business plans for assigned franchises/licenses in SharePoint.
  • Assist in preparing technical presentations and meetings with regulators.
  • Gather and assemble information, and prepare documents for new product applications, renewal applications, change notifications, and responses to regulatory agency questions.
  • Maintain changes to regulations, products, and sites, making necessary submissions to maintain compliance.
  • Coordinate with internal stakeholders to ensure compliant lifecycle management of products/franchises.
  • Maintain the regulatory affairs database for responsible franchises in the MDRIM tool.
  • Ensure timely completion of change assessments, quality issues, and corrective actions.
  • Create and maintain product registration request forms and change controls.
  • Ensure timely archival of regulatory submission documents.
  • Participate in the execution of field actions such as product recalls and distribution of field safety alerts, completing assigned tasks promptly.
  • Understand and report complaints and adverse events promptly.
  • Undertake other assignments as identified and assigned by supervisor/management.

Special Requirements:
You should have strong knowledge of the Medical Device Rule 2017 and the Drugs and Cosmetics Act. Familiarity with international regulations for medical devices in the US and EU is desirable. Proficiency in Medical Device Quality Management System ISO 13485 is also required, along with excellent computer skills and technical writing abilities.

Qualifications:

  • Graduate/Postgraduate in Lifescience/Biomedical/Pharmacy.
  • Minimum 2-6 years of industry experience in regulatory affairs, preferably in medical devices.
  • Experience in submitting, registering, and maintaining product registrations with the Ministry of Health.
  • Experience in quality/manufacturing and regulatory affairs in medical devices is advantageous.
  • Experience in assembling product dossiers for submission to regulatory authorities.
  • Good technical writing and communication skills.
Application Link


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