Medical content writer

at ZenOnco

Medical content writer

ZenOnco

Company

Home

Medical content writer

at ZenOnco

Posted by Dimple Parmar

4 - 9 yrs

₹5L - ₹9L / yr (ESOP available)

Mumbai

Skills

Medical writing

Content Writing

Pharmacology

Content Marketing

Medical content writer

Salary: 5-9 LPA

About ZenOnco.io:

https://zenonco.io/">ZenOnco.io is the world’s first integrative oncology healthtech platform. At ZenOnco.io, we aim to extend life and improve the quality of life for cancer patients through integrative oncology treatment, which covers both medical treatment as well as complementary treatment (Nutrition, emotional wellness, fitness, and community support).

To provide the best medical treatment options to cancer patients, we have partnered with 50+ hospitals across India, and cover 1,000+ oncologists. We also provide patients access to a full range of diagnostic tests that are required to arrive at the most effective cancer treatment.

We heavily deploy technology in our operations, and have recently launched the world’s first Integrative Oncology Preliminary Assessment Report tool (ZIOPAR) to guide cancer patients free of cost on the possible treatment options based on their cancer profile, symptoms and other conditions.

We believe in innovation, dedication and commitment. While we have the thrill to seek out and capture the world, we are looking for a responsible partner in you. If you feel you can become one of us, apply today.

Company introduction video: https://bit.ly/ZenOncoIOintroduction">https://bit.ly/ZenOncoIOintroduction

Role and responsibility:

Acts as Lead Medical Writer and performs competently on straightforward projects, with guidance from senior staff as required. Takes responsibility for preparation of assigned documents to a high standard, working in accordance with Quintiles SOPs and the customer’s requirements. Identifies project needs, tracks project timelines and implements client requests with senior review.

Participates in both internal and external project team meetings and liaises directly with the customer on medical writing issues, as appropriate and with senior support as needed.
Arranges appropriate internal review of assigned documents and takes responsibility for on-time delivery.
May perform QC review of documents or parts of documents prepared by more senior staff.
Takes responsibility for managing day-to-day workload for assigned tasks and projects, in collaboration with senior staff.
Keeps abreast of current data, trends, medical writing/regulatory knowledge, developments and advances in area of drug development/medical writing.
Complies with Company SOPs and participates in the implementation of new SOPs.

Required knowledge, skills, and abilities:

Excellent standard of written English, and ability to communicate fluently and effectively in English, both in writing and verbally.

Familiarity with the structural and content requirements of clinical study reports, protocols, and similar documents.
Ability to integrate, interpret, and summarize data from a variety of sources in a clear and concise manner.
Competence in completing a good first draft clinical study report in a routine therapeutic area within a reasonable timeframe with limited guidance.
Good understanding of common statistical methods used in clinical trials and interpretation of their results.
Ability to give a simple presentation to a project team and/or customer, e.g. on Medical Writing processes.
Ability to identify inconsistencies and deficiencies in statistical output.
Coordinate with various technical professionals to gather, organize and compile information on new products or processes
Go through medical topics and assist physicians in writing research related articles and reviews
Assist in preparing press releases, training material and marketing content
Write articles and reports on research discoveries connected to health and medical fields
Communicate complex medical information in a succinct way
Work with clinical researchers in the development of research protocols
Participate in the preparation of various clinical research and regulatory documents
Prepare annual reports, brochures, abstracts and presentations
Prepare training materials and eLearning content according to the needs of the audience
Make sure all applicable guidelines and regulations are followed
Stay up to date on current industry practices and regulations
Knowledge of regulations relevant to medical writing

Education and Experience:

Bachelor’s or Master’s degree in a life science-related discipline, plus at least 4 years+ experience as a medical writer within a pharmaceutical environment; or equivalent combination of education, training and experience.

You will get:

Some of the best people to work with (founders are IIM graduates and investment banker)
An opportunity to make a difference in the lives of millions of cancer patients across the globe
A great learning environment and opportunity to grow

Medical content writer

Salary: 5-9 LPA

About ZenOnco.io:

Company introduction video: https://bit.ly/ZenOncoIOintroduction">https://bit.ly/ZenOncoIOintroduction

Role and responsibility:

Participates in both internal and external project team meetings and liaises directly with the customer on medical writing issues, as appropriate and with senior support as needed.
Arranges appropriate internal review of assigned documents and takes responsibility for on-time delivery.
May perform QC review of documents or parts of documents prepared by more senior staff.
Takes responsibility for managing day-to-day workload for assigned tasks and projects, in collaboration with senior staff.
Keeps abreast of current data, trends, medical writing/regulatory knowledge, developments and advances in area of drug development/medical writing.
Complies with Company SOPs and participates in the implementation of new SOPs.

Required knowledge, skills, and abilities:

Excellent standard of written English, and ability to communicate fluently and effectively in English, both in writing and verbally.

Familiarity with the structural and content requirements of clinical study reports, protocols, and similar documents.
Ability to integrate, interpret, and summarize data from a variety of sources in a clear and concise manner.
Competence in completing a good first draft clinical study report in a routine therapeutic area within a reasonable timeframe with limited guidance.
Good understanding of common statistical methods used in clinical trials and interpretation of their results.
Ability to give a simple presentation to a project team and/or customer, e.g. on Medical Writing processes.
Ability to identify inconsistencies and deficiencies in statistical output.
Coordinate with various technical professionals to gather, organize and compile information on new products or processes
Go through medical topics and assist physicians in writing research related articles and reviews
Assist in preparing press releases, training material and marketing content
Write articles and reports on research discoveries connected to health and medical fields
Communicate complex medical information in a succinct way
Work with clinical researchers in the development of research protocols
Participate in the preparation of various clinical research and regulatory documents
Prepare annual reports, brochures, abstracts and presentations
Prepare training materials and eLearning content according to the needs of the audience
Make sure all applicable guidelines and regulations are followed
Stay up to date on current industry practices and regulations
Knowledge of regulations relevant to medical writing

Education and Experience:

You will get:

Some of the best people to work with (founders are IIM graduates and investment banker)
An opportunity to make a difference in the lives of millions of cancer patients across the globe
A great learning environment and opportunity to grow

Users love Cutshort

Read about what our users have to say about finding their next opportunity on Cutshort.

Shubham Vishwakarma

Full Stack Developer - Averlon

I had an amazing experience. It was a delight getting interviewed via Cutshort. The entire end to end process was amazing. I would like to mention Reshika, she was just amazing wrt guiding me through the process. Thank you team.

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About ZenOnco

Founded :

2019

Type :

Products & Services

Size :

20-100

Stage :

Bootstrapped

About

ZenOnco.io counsels cancer patients on integrative therapies.

We are an ambitious start-up aiming to grow at an exponential rate. Both Co-Founders are highly committed people and have left lucrative careers to grow ZenOnco.io.

One Co-Founder is personally close to the cause of cancer due to loss in family; another Co-Founder is an ex-investment banker and ex-private equity investor. Both Co-Founders have complementary skills, and are hungry for exponential growth. They are also highly educated (IIM Calcutta, CA, CFA, FRM, CAIA, M.Com, B. Tech) and have combined ~12 years of prior work exp across J.P. Morgan, GIC, EY, Reliance Industries, BNY Mellon).

Our service is unique with virtually nil or very small competitors.

There is a huge scope to grow with us.

ZenOnco.io counsels cancer patients on integrative therapies.

We are an ambitious start-up aiming to grow at an exponential rate. Both Co-Founders are highly committed people and have left lucrative careers to grow ZenOnco.io.

Our service is unique with virtually nil or very small competitors.

There is a huge scope to grow with us.

Connect with the team

Monali Modak

Connect

Dimple Parmar

Connect

Company social profiles

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+3 more

Looking only for immediate to 15 days candidate.
Looking for an experienced Integration specialist with a good expertise in ETL Informatica and a strong Application integration background
Minimum of 3+ years relevant experience in Informatica MDM required. Powercenter is a core skill set.
Having experience in a broader Informatica toolset is strongly preferred
Should prove a very strong implementation experience in Application integration, should demonstrate expertise/presentation with multiple use cases
Passionate coders with a strong Application development background, years of experience could range from 5+ to 15+
Should have application development experience outside of ETL, (just learning ETL as a tool is not enough), experience in writing application outside of ETL will bring in more value
Strong database skills with a strong understanding of data, data quality, data governance, understanding and developing standalone and integrated database layers (sql, packages, functions, performance tuning ), i.e. Expert with a strong integration background who has more application integration background than just an ETL Informatica tool
Experience in integration with XML/JSON based and heavily involve JMS MQ (read/write)
Experience in SOAP and REST based API's exchanging both XML and JSON files used for request and response
Experience with Salesforce.com Integration using Informatica power exchange module is a plus but not needed
Experience with Informatica MDM as a technology stack that is used for integration of senior market members with Salesforce.com is a plus but not needed,
Very strong scripting background (C/bourne shell/Perl/Java)
Should be able to understand JAVA, we do have development around JAVA, i.e ability to work around a solution in programming language like Java when implementation is not possible through ETL
Ability to communicate effectively via multiple channels (verbal, written, etc.) with technical and non-technical staff.

Looking only for immediate to 15 days candidate.
Looking for an experienced Integration specialist with a good expertise in ETL Informatica and a strong Application integration background
Minimum of 3+ years relevant experience in Informatica MDM required. Powercenter is a core skill set.
Having experience in a broader Informatica toolset is strongly preferred
Should prove a very strong implementation experience in Application integration, should demonstrate expertise/presentation with multiple use cases
Passionate coders with a strong Application development background, years of experience could range from 5+ to 15+
Should have application development experience outside of ETL, (just learning ETL as a tool is not enough), experience in writing application outside of ETL will bring in more value
Strong database skills with a strong understanding of data, data quality, data governance, understanding and developing standalone and integrated database layers (sql, packages, functions, performance tuning ), i.e. Expert with a strong integration background who has more application integration background than just an ETL Informatica tool
Experience in integration with XML/JSON based and heavily involve JMS MQ (read/write)
Experience in SOAP and REST based API's exchanging both XML and JSON files used for request and response
Experience with Salesforce.com Integration using Informatica power exchange module is a plus but not needed
Experience with Informatica MDM as a technology stack that is used for integration of senior market members with Salesforce.com is a plus but not needed,
Very strong scripting background (C/bourne shell/Perl/Java)
Should be able to understand JAVA, we do have development around JAVA, i.e ability to work around a solution in programming language like Java when implementation is not possible through ETL
Ability to communicate effectively via multiple channels (verbal, written, etc.) with technical and non-technical staff.

Full stack developer

at Zoomtail

1 recruiter

Posted by Varun Jain

Bengaluru (Bangalore)

3 - 5 yrs

₹8L - ₹15L / yr

NodeJS (Node.js)

Python

Javascript

We are looking for software development engineers to form our initial core team to design and develop our marketplace platforms from scratch. These include scalable backend platform and frontend applications for customer & seller apps, demand generation platform, supply chain & logistics platform, and several cross platform components. As an early stage startup growing at fast pace, we are looking for leaders who have the hunger to work with some of the smartest people, and leave a legacy. The work we do will impact real lives, and has the potential to bring positive change to a billion people by fundamentally changing the face of the B2B ecosystem in India, leave a legacy in the country, and in the technology fraternity.

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