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Associate Medical Coding Professional

**Category**:Data & AI**Location**:Bangalore, Karnataka, IN**Department**:Data Systems & Automation, Bangalore Global Development GBS (DSA,BGD)-
**About the Department**
- Data Systems & Automation (DSA), Data Management, Bengaluru is one of the most competent and diverse team of professionals who are mainly responsible for providing functional and system support to execute clinical trials across Product Development Plan portfolio. The team has strong understanding of Clinical Systems & interfaces with end-to-start mindset on standardisation of data-flow across systems, Electronic Case Report Form (ECRF) development using Central Designer and knowledge with Clinical Data Interchange Standards Consortium (CDISC) concepts annotated Case Report Form (aCRF), Study Data Tabulation Model (SDTM) mapping, SAS programming, Study Data Review Guideline (SDRG) etc., to aid CDISC submission which is a mandate from regulatory authorities.**The Position**
- As an Associate Medical Coding Professional, primary responsibility will be to perform timely and accurate categorization of verbatim text in assigned clinical trials to standard medical dictionaries and nomenclature such as MedDRA and WHODrug Global using the TMS Application. You will also be responsible for performing ATC coding on concomitant medications with multiple ATC codes based on project/trial requirements,ensuring compliance with internal and external coding procedures by coordinating with Senior/Medical Coding Professional and Global Safety, and maintaining contact with relevant external organizations. Additionally, you will be required to report on the status of coding of clinical trials to keep all stakeholders informed. Your role will be critical in ensuring the accuracy and compliance of clinical trial data.- .- Perform timely and accurate categorization of verbatim text in assigned clinical trials to standard medical dictionaries and nomenclature (MedDRA and WHODrug Global) using the TMS Application
- Perform ATC coding on concomitant medications with multiple ATC codes based on project/trial requirements
- Ensure compliance with internal and external coding procedures by coordinating with Senior/Medical Coding Professional and Global Safety, and maintain contact with relevant external organizations
- Report on the status of coding of clinical trials

**Experience**
- M.Sc / B.Sc in Life Science or comparable degree in medicine, nursing, pharmacy, veterinary science or clinical information management or equivalent qualifications
- Preferably 3 years of data management experience and the majority of this within Pharma industry or Development
- Preferably knowledge of Medical Coding dictionaries
- Preferably experience in project management
- Ability and willingness to adjust quickly to new situations in a continuously developing environment
- Team oriented personality with high degree of flexibility and cross-cultural awareness
- Understanding of project management
- Knowledge of ICH/GCP and drug development preferable

**Working At Novo Nordisk**
- At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales
- we're all working to move the needle on patient care.**Contact**Deadline**- We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.- At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.

**Purpose**:
**Organization Background**

Our Medical Affairs Quality Content Review Group is dedicated to ensuring the highest standards of medical quality, accuracy, and compliance across all our endeavors, ensuring our customers receive accurate and timely information. Our commitment to excellence fosters a culture of trust between our internal and external stakeholders.

**Position Description**

The Quality-Medical Affairs Professional (Q-MAP (Quality Medical Affairs Professional)) is a therapeutically aligned clinical scientist focusing on the quality reviewing of deliverables for both promotional and non-promotional content. Q-MAPSs will play a key role within the medical affairs organization. The primary focus of the Quality-Medical Affairs Professional is to use the individual’s knowledge of specific disease states and available treatments to provide scientific and creative input, contribute to the development, review, and approval of promotional and medical materials. The MAP plays a significant role in the cross-functional partnership with the brand team and medical affairs business units to meet both external customer and internal business needs. Refer to the _Guidance for Implementation of the Medical Affairs Professional Role _for additional information.

**Primary Responsibilities**

This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. Consult with your supervision regarding your actual job responsibilities and any related duties that may be required for the position.

**Brand Team Support**:
Serve as a key medical point of contact for the brand team:

- Contribute clinical, scientific knowledge to support the cross functional team.
- Contribute to the development of local brand plans & medical strategies.
- By offering scientific and creative input, contribute to the development (local materials) and/or review (global/regional materials) of promotional and non
- promotional materials.
- Effectively communicate and transfer knowledge of the therapeutic available solutions environment, the clinical landscape and relevant medical and scientific information.

Support the medical training needs of internal business partners.

**Scientific Expertise and Medical Affairs Delivery**:

- Support data analysis and the development of slide sets and publications (abstracts, posters, manuscripts).
- Partner with other existing medical affairs roles (e.g., CRP (Clinical Research Physician), CRS (Clinical Research Scientist), MSLs (Medical Science Liaisons)) to achieve a seamless medical team aimed at delivering exceptional customer experiences.
- Ability to offer scientific and creative input, contribute to the development and/or review (global/regional materials) of promotional and non
- promotional materials.
- Support Scientific Data Disclosure (SDD plans)Critically read and evaluate relevant medical literature to be current in the therapeutic area.
- Keep up to date with medical and other scientific developments relevant to the product or portfolio.
- Be aware of current trends, issues and projections for clinical practice and access.

**Minimum Qualification Requirements**
- Advanced degree (MD, PHD etc.) in health sciences plus 2 years of relevant clinical or therapeutic experience

OR
- Master’s or Bachelor’s degree (MBBS, BDS (Dental Surgery), PharmD, MSc Nursing, etc.) in health sciences considered with 2 years of clinical experience.
- Relevant scientific industry experience
- Advanced interpersonal, communication, teamwork, project management.
- Ability to ‘translate’ scientific data into meaningful, clear, and compliant content for customer communications and engagement.
- Knowledge and experience at the customer interface.
- Ability to effectively partner across multiple functions including but not limited to Marketing, Compliance, Legal, Regulatory, payer, strong leadership, and ability to influence, including upward.
- High workload capacity including ability to manage and prioritize broad deliverables of a complex nature.

**Other Information/Additional Preferences**

The Q-MAP role is office-based or hybrid
- based (if geographically necessary), not field-based.

Lilly does not discriminate on the basis of age, race, color, r

**Designation**: Trainee - BE / B.Tech - Electrical/Electronics/Biomedical - Fresher

**Location**: gandhinagar

**Edu.Qualification**: B.E. / B.Tech - Electrical/ Electronics/Biomedical

**Experience**: 0 - 0 Years

**Greetings from Starworth Global Solutions!**

**Medical Coder Specialized in ED (Professional)**

**Experience
- 1 + years**

**Salary: MAX 45k**

**Location: Chennai.**

**Experience**:

- **Medical Coding: 1 year (preferred)**:

- **ED Professional Coding: 1 year (preferred)**:

- **Experience in Emergency coding is preferred**

**License/Certification**:

- **CPC, CIC, COC (mandatory)**

**Salary**: Up to ₹40,000.00 per month

**Benefits**:

- Health insurance

Schedule:

- Day shift
- Flexible shift

Supplemental pay types:

- Performance bonus

Ability to commute/relocate:

- Hyderabad, Telangana: Reliably commute or planning to relocate before starting work (required)

**Experience**:

- total work: 1 year (preferred)
- Medical Coding: 1 year (preferred)

License/Certification:

- CPC, CIC, COC (preferred)

**Speak with the employer**

+91

Overview:

Please Note: You may be required to travel to our Mumbai office based on business requirements or for company/team events.

If you are looking for challenging and rewarding work which combines your understanding of medical science and aptitude for writing into one unique job, the Medical Writer role is for you. This is an opportunity to grow your career and make a greater impact on the lives around you.

Job Responsibilities:

• Use scientific expertise to develop (write, proofread, and data-check) high-quality, client-ready scientific, medical, and educational materials like slides, abstracts, posters, manuscripts, MSL/training slide decks, infographics, congress and meetings materials, literature searches and reviews, standard response letters/medical information letters, and HCP engagement content according to client needs with excellent attention to detail under the guidance of the scientific leads
• Liaise and build trusting and professional relationships with international pharmaceutical clients, healthcare professionals, internal and external stakeholders including authors, reviewers and key opinion leaders across therapeutic areas -- learning to anticipate their needs
• Effectively and proactively communicate with team members, authors/faculty, clients and vendors
• Attend workshops/seminars/trainings to hone your skills and contribute to organizational objectives
• Attend client and other external meetings and supporting senior team members as needed
• Apply your scientific and creative knowledge and work closely with client directors in developing ideas and executing effective medical communications initiatives in the digital space, including publication extenders, creation of infographics, interactive assets, website content, patient narratives, and medical information engagement plans
• You will be responsible for ensuring all materials follow/comply with client requirements/SOPs, style guides, client templates, client preferences (as applicable), and CACTUS’ internal SOPs. Any updates to either of these items should be made consistently and documents should remain up to date.
• Perform as a document specialist, provide intellectual input across document types, and contribute to making cutting-edge research accessible to specific audiences as appropriate, by maintaining current awareness of developments across therapeutic areas or disciplines
• Share best practices and client preferences, thereby contributing to skill development within the medical communications team

Requirements:

• 1-3 years of experience in relevant fields of scientific writing
• PhD/MD (Pharmacology) OR PhD (Life Sciences) OR PharmD with a good understanding of clinical research and medical communication
• Clear, concise, scientific style of writing, with a high level of attention to detail and excellent language skills
• Excellent communication skills, especially with the clients
• Ability to adapt writing style to different materials and target audiences
• Basic knowledge of biostatistics
• Literature reviewing and evaluation capabilities
• Very good working knowledge of MS Office

Application Process:

Before applying, please ensure you meet the role requirements listed above and have legal authorization to work in the country where this role is advertised. Our selection process typically involves an initial screening by a recruiter, a technical assessment, and two to three interview rounds.

Equal Opportunity

Our hiring practices reflect our commitment to providing equal opportunities and creating an environment where everyone can thrive, develop, and succeed. We celebrate the uniqueness of our team members and prohibit discrimination of any kind, based on race, color, religion, gender identity, sexual orientation, age, marital status, disability, or any other protected characteristic.

Accelerating from Anywhere

As a remote-first organization, these are essential attributes we look for in all our candidates.

• Taking ownership of your work with minimal supervision, showing strong ability to organize, prioritize and deliver results independently.
• Documenting work that brings everyone on the same page.
• Maturity to choose between synchronous and asynchronous collaboration.
• Effectively collaborating with colleagues across different time zones by setting dedicated hours for collaboration and keeping team members updated through your MS Teams status.

About US:

At Cactus Life Sciences (cactuslifesciences.com), we believe the future of medical communications lies at the intersection of science, technology, and human connection. Headquartered in Princeton, New Jersey, with teams in Switzerland, the United Kingdom, India, and Japan, we help biopharmaceutical organizations redefine scientific exchange—leveraging AI, automation, and innovation while keeping patients at the heart of everything we do.

Our expertise spans medical strategy, scientific content development, and medical education across therapeutic areas and the product lifecycle. By blending scientific rigor, agile operational models, and future-ready technologies, we partner with medical affairs teams to catalyze their transformation, adapt to a changing landscape, and drive meaningful outcomes for healthcare communities worldwide.

Overview:

Please Note: You may be required to travel to our Mumbai office based on business requirements or for company/team events.

If you are looking for challenging and rewarding work which combines your understanding of medical science and aptitude for writing into one unique job, the Medical Writer role is for you. This is an opportunity to grow your career and make a greater impact on the lives around you.

Job Responsibilities:

- Use scientific expertise to develop (write, proofread, and data-check) high-quality, client-ready scientific, medical, and educational materials like slides, abstracts, posters, manuscripts, MSL/training slide decks, infographics, congress and meetings materials, literature searches and reviews, standard response letters/medical information letters, and HCP engagement content according to client needs with excellent attention to detail under the guidance of the scientific leads
- Liaise and build trusting and professional relationships with international pharmaceutical clients, healthcare professionals, internal and external stakeholders including authors, reviewers and key opinion leaders across therapeutic areas -- learning to anticipate their needs
- Effectively and proactively communicate with team members, authors/faculty, clients and vendors
- Attend workshops/seminars/trainings to hone your skills and contribute to organizational objectives
- Attend client and other external meetings and supporting senior team members as needed
- Apply your scientific and creative knowledge and work closely with client directors in developing ideas and executing effective medical communications initiatives in the digital space, including publication extenders, creation of infographics, interactive assets, website content, patient narratives, and medical information engagement plans
- You will be responsible for ensuring all materials follow/comply with client requirements/SOPs, style guides, client templates, client preferences (as applicable), and CACTUS’ internal SOPs. Any updates to either of these items should be made consistently and documents should remain up to date.
- Perform as a document specialist, provide intellectual input across document types, and contribute to making cutting-edge research accessible to specific audiences as appropriate, by maintaining current awareness of developments across therapeutic areas or disciplines
- Share best practices and client preferences, thereby contributing to skill development within the medical communications team

Requirements:

- 1-3 years of experience in relevant fields of scientific writing
- PhD/MD (Pharmacology) OR PhD (Life Sciences) OR PharmD with a good understanding of clinical research and medical communication
- Clear, concise, scientific style of writing, with a high level of attention to detail and excellent language skills
- Excellent communication skills, especially with the clients
- Ability to adapt writing style to different materials and target audiences
- Basic knowledge of biostatistics
- Literature reviewing and evaluation capabilities
- Very good working knowledge of MS Office

Application Process:

Before applying, please ensure you meet the role requirements listed above and have legal authorization to work in the country where this role is advertised. Our selection process typically involves an initial screening by a recruiter, a technical assessment, and two to three interview rounds.

Equal Opportunity

Our hiring practices reflect our commitment to providing equal opportunities and creating an environment where everyone can thrive, develop, and succeed. We celebrate the uniqueness of our team members and prohibit discrimination of any kind, based on race, color, religion, gender identity, sexual orientation, age, marital status, disability, or any other protected characteristic.

Accelerating from Anywhere

As a remote-first organization, these are essential attributes we look for in all our candidates.

- Taking ownership of your work with minimal supervision, showing strong ability to organize, prioritize and deliver results independently.
- Documenting work that brings everyone on the same page.
- Maturity to choose between synchronous and asynchronous collaboration.
- Effectively collaborating with colleagues across different time zones by setting dedicated hours for collaboration and keeping team members updated through your MS Teams status.

About US:

At Cactus Life Sciences (cactuslifesciences.com), we believe the future of medical communications lies at the intersection of science, technology, and human connection. Headquartered in Princeton, New Jersey, with teams in Switzerland, the United Kingdom, India, and Japan, we help biopharmaceutical organizations redefine scientific exchange—leveraging AI, automation, and innovation while keeping patients at the heart of everything we do.

Our expertise spans medical strategy, scientific content development, and medical education across therapeutic areas and the product lifecycle. By blending scientific rigor, agile operational models, and future-ready technologies, we partner with medical affairs teams to catalyze their transformation, adapt to a changing landscape, and drive meaningful outcomes for healthcare communities worldwide.

Overview:

Please Note: You may be required to travel to our Mumbai office based on business requirements or for company/team events.

If you are looking for challenging and rewarding work which combines your understanding of medical science and aptitude for writing into one unique job, the Medical Writer role is for you. This is an opportunity to grow your career and make a greater impact on the lives around you.

Job Responsibilities:

• Use scientific expertise to develop (write, proofread, and data-check) high-quality, client-ready scientific, medical, and educational materials like slides, abstracts, posters, manuscripts, MSL/training slide decks, infographics, congress and meetings materials, literature searches and reviews, standard response letters/medical information letters, and HCP engagement content according to client needs with excellent attention to detail under the guidance of the scientific leads
• Liaise and build trusting and professional relationships with international pharmaceutical clients, healthcare professionals, internal and external stakeholders including authors, reviewers and key opinion leaders across therapeutic areas -- learning to anticipate their needs
• Effectively and proactively communicate with team members, authors/faculty, clients and vendors
• Attend workshops/seminars/trainings to hone your skills and contribute to organizational objectives
• Attend client and other external meetings and supporting senior team members as needed
• Apply your scientific and creative knowledge and work closely with client directors in developing ideas and executing effective medical communications initiatives in the digital space, including publication extenders, creation of infographics, interactive assets, website content, patient narratives, and medical information engagement plans
• You will be responsible for ensuring all materials follow/comply with client requirements/SOPs, style guides, client templates, client preferences (as applicable), and CACTUS’ internal SOPs. Any updates to either of these items should be made consistently and documents should remain up to date.
• Perform as a document specialist, provide intellectual input across document types, and contribute to making cutting-edge research accessible to specific audiences as appropriate, by maintaining current awareness of developments across therapeutic areas or disciplines
• Share best practices and client preferences, thereby contributing to skill development within the medical communications team

Requirements:

• 1-3 years of experience in relevant fields of scientific writing
• PhD/MD (Pharmacology) OR PhD (Life Sciences) OR PharmD with a good understanding of clinical research and medical communication
• Clear, concise, scientific style of writing, with a high level of attention to detail and excellent language skills
• Excellent communication skills, especially with the clients
• Ability to adapt writing style to different materials and target audiences
• Basic knowledge of biostatistics
• Literature reviewing and evaluation capabilities
• Very good working knowledge of MS Office

Application Process:

Before applying, please ensure you meet the role requirements listed above and have legal authorization to work in the country where this role is advertised. Our selection process typically involves an initial screening by a recruiter, a technical assessment, and two to three interview rounds.

Equal Opportunity

Our hiring practices reflect our commitment to providing equal opportunities and creating an environment where everyone can thrive, develop, and succeed. We celebrate the uniqueness of our team members and prohibit discrimination of any kind, based on race, color, religion, gender identity, sexual orientation, age, marital status, disability, or any other protected characteristic.

Accelerating from Anywhere

As a remote-first organization, these are essential attributes we look for in all our candidates.

• Taking ownership of your work with minimal supervision, showing strong ability to organize, prioritize and deliver results independently.
• Documenting work that brings everyone on the same page.
• Maturity to choose between synchronous and asynchronous collaboration.
• Effectively collaborating with colleagues across different time zones by setting dedicated hours for collaboration and keeping team members updated through your MS Teams status.

About US:

At Cactus Life Sciences (cactuslifesciences.com), we believe the future of medical communications lies at the intersection of science, technology, and human connection. Headquartered in Princeton, New Jersey, with teams in Switzerland, the United Kingdom, India, and Japan, we help biopharmaceutical organizations redefine scientific exchange—leveraging AI, automation, and innovation while keeping patients at the heart of everything we do.

Our expertise spans medical strategy, scientific content development, and medical education across therapeutic areas and the product lifecycle. By blending scientific rigor, agile operational models, and future-ready technologies, we partner with medical affairs teams to catalyze their transformation, adapt to a changing landscape, and drive meaningful outcomes for healthcare communities worldwide.

Overview:

Please Note: You may be required to travel to our Mumbai office based on business requirements or for company/team events.

If you are looking for challenging and rewarding work which combines your understanding of medical science and aptitude for writing into one unique job, the Medical Writer role is for you. This is an opportunity to grow your career and make a greater impact on the lives around you.

Job Responsibilities:

• Use scientific expertise to develop (write, proofread, and data-check) high-quality, client-ready scientific, medical, and educational materials like slides, abstracts, posters, manuscripts, MSL/training slide decks, infographics, congress and meetings materials, literature searches and reviews, standard response letters/medical information letters, and HCP engagement content according to client needs with excellent attention to detail under the guidance of the scientific leads
• Liaise and build trusting and professional relationships with international pharmaceutical clients, healthcare professionals, internal and external stakeholders including authors, reviewers and key opinion leaders across therapeutic areas -- learning to anticipate their needs
• Effectively and proactively communicate with team members, authors/faculty, clients and vendors
• Attend workshops/seminars/trainings to hone your skills and contribute to organizational objectives
• Attend client and other external meetings and supporting senior team members as needed
• Apply your scientific and creative knowledge and work closely with client directors in developing ideas and executing effective medical communications initiatives in the digital space, including publication extenders, creation of infographics, interactive assets, website content, patient narratives, and medical information engagement plans
• You will be responsible for ensuring all materials follow/comply with client requirements/SOPs, style guides, client templates, client preferences (as applicable), and CACTUS’ internal SOPs. Any updates to either of these items should be made consistently and documents should remain up to date.
• Perform as a document specialist, provide intellectual input across document types, and contribute to making cutting-edge research accessible to specific audiences as appropriate, by maintaining current awareness of developments across therapeutic areas or disciplines
• Share best practices and client preferences, thereby contributing to skill development within the medical communications team

Requirements:

• 1-3 years of experience in relevant fields of scientific writing
• PhD/MD (Pharmacology) OR PhD (Life Sciences) OR PharmD with a good understanding of clinical research and medical communication
• Clear, concise, scientific style of writing, with a high level of attention to detail and excellent language skills
• Excellent communication skills, especially with the clients
• Ability to adapt writing style to different materials and target audiences
• Basic knowledge of biostatistics
• Literature reviewing and evaluation capabilities
• Very good working knowledge of MS Office

Application Process:

Before applying, please ensure you meet the role requirements listed above and have legal authorization to work in the country where this role is advertised. Our selection process typically involves an initial screening by a recruiter, a technical assessment, and two to three interview rounds.

Equal Opportunity

Our hiring practices reflect our commitment to providing equal opportunities and creating an environment where everyone can thrive, develop, and succeed. We celebrate the uniqueness of our team members and prohibit discrimination of any kind, based on race, color, religion, gender identity, sexual orientation, age, marital status, disability, or any other protected characteristic.

Accelerating from Anywhere

As a remote-first organization, these are essential attributes we look for in all our candidates.

• Taking ownership of your work with minimal supervision, showing strong ability to organize, prioritize and deliver results independently.
• Documenting work that brings everyone on the same page.
• Maturity to choose between synchronous and asynchronous collaboration.
• Effectively collaborating with colleagues across different time zones by setting dedicated hours for collaboration and keeping team members updated through your MS Teams status.

About US:

At Cactus Life Sciences (cactuslifesciences.com), we believe the future of medical communications lies at the intersection of science, technology, and human connection. Headquartered in Princeton, New Jersey, with teams in Switzerland, the United Kingdom, India, and Japan, we help biopharmaceutical organizations redefine scientific exchange—leveraging AI, automation, and innovation while keeping patients at the heart of everything we do.

Our expertise spans medical strategy, scientific content development, and medical education across therapeutic areas and the product lifecycle. By blending scientific rigor, agile operational models, and future-ready technologies, we partner with medical affairs teams to catalyze their transformation, adapt to a changing landscape, and drive meaningful outcomes for healthcare communities worldwide.

Overview:

Please Note: You may be required to travel to our Mumbai office based on business requirements or for company/team events.

If you are looking for challenging and rewarding work which combines your understanding of medical science and aptitude for writing into one unique job, the Medical Writer role is for you. This is an opportunity to grow your career and make a greater impact on the lives around you.

Job Responsibilities:

• Use scientific expertise to develop (write, proofread, and data-check) high-quality, client-ready scientific, medical, and educational materials like slides, abstracts, posters, manuscripts, MSL/training slide decks, infographics, congress and meetings materials, literature searches and reviews, standard response letters/medical information letters, and HCP engagement content according to client needs with excellent attention to detail under the guidance of the scientific leads
• Liaise and build trusting and professional relationships with international pharmaceutical clients, healthcare professionals, internal and external stakeholders including authors, reviewers and key opinion leaders across therapeutic areas -- learning to anticipate their needs
• Effectively and proactively communicate with team members, authors/faculty, clients and vendors
• Attend workshops/seminars/trainings to hone your skills and contribute to organizational objectives
• Attend client and other external meetings and supporting senior team members as needed
• Apply your scientific and creative knowledge and work closely with client directors in developing ideas and executing effective medical communications initiatives in the digital space, including publication extenders, creation of infographics, interactive assets, website content, patient narratives, and medical information engagement plans
• You will be responsible for ensuring all materials follow/comply with client requirements/SOPs, style guides, client templates, client preferences (as applicable), and CACTUS’ internal SOPs. Any updates to either of these items should be made consistently and documents should remain up to date.
• Perform as a document specialist, provide intellectual input across document types, and contribute to making cutting-edge research accessible to specific audiences as appropriate, by maintaining current awareness of developments across therapeutic areas or disciplines
• Share best practices and client preferences, thereby contributing to skill development within the medical communications team

Requirements:

• 1-3 years of experience in relevant fields of scientific writing
• PhD/MD (Pharmacology) OR PhD (Life Sciences) OR PharmD with a good understanding of clinical research and medical communication
• Clear, concise, scientific style of writing, with a high level of attention to detail and excellent language skills
• Excellent communication skills, especially with the clients
• Ability to adapt writing style to different materials and target audiences
• Basic knowledge of biostatistics
• Literature reviewing and evaluation capabilities
• Very good working knowledge of MS Office

Application Process:

Before applying, please ensure you meet the role requirements listed above and have legal authorization to work in the country where this role is advertised. Our selection process typically involves an initial screening by a recruiter, a technical assessment, and two to three interview rounds.

Equal Opportunity

Our hiring practices reflect our commitment to providing equal opportunities and creating an environment where everyone can thrive, develop, and succeed. We celebrate the uniqueness of our team members and prohibit discrimination of any kind, based on race, color, religion, gender identity, sexual orientation, age, marital status, disability, or any other protected characteristic.

Accelerating from Anywhere

As a remote-first organization, these are essential attributes we look for in all our candidates.

• Taking ownership of your work with minimal supervision, showing strong ability to organize, prioritize and deliver results independently.
• Documenting work that brings everyone on the same page.
• Maturity to choose between synchronous and asynchronous collaboration.
• Effectively collaborating with colleagues across different time zones by setting dedicated hours for collaboration and keeping team members updated through your MS Teams status.

About US:

At Cactus Life Sciences (cactuslifesciences.com), we believe the future of medical communications lies at the intersection of science, technology, and human connection. Headquartered in Princeton, New Jersey, with teams in Switzerland, the United Kingdom, India, and Japan, we help biopharmaceutical organizations redefine scientific exchange—leveraging AI, automation, and innovation while keeping patients at the heart of everything we do.

Our expertise spans medical strategy, scientific content development, and medical education across therapeutic areas and the product lifecycle. By blending scientific rigor, agile operational models, and future-ready technologies, we partner with medical affairs teams to catalyze their transformation, adapt to a changing landscape, and drive meaningful outcomes for healthcare communities worldwide.