Analyst - Therapeutics Job at Modoras Accounting Syd (Mumbai)

Junior Cybersecurity Analyst

We are seeking a highly motivated Junior Cybersecurity Analyst Contractor to joi...

Location

United States , New York

Salary:

60.00 - 70.00 USD / Hour

Click Therapeutics

Expiration Date

Until further notice

Requirements

2+ years of experience required
Strong project management skills
Excellent communication skills
Strong organization and attention to details

Job Responsibility

Utilize Jira to effectively manage and prioritize technical cybersecurity projects, ensuring clear task assignments, progress tracking, and timely completion
Develop and maintain detailed project plans, timelines, and resource allocation within Jira
Monitor project milestones, identify potential roadblocks, and proactively implement solutions
Maintain accurate and up-to-date project documentation within Jira
Serve as the primary point of contact for project-related communication, coordinating with internal teams (security, development) and external partners
Clearly and concisely communicate technical project updates, priorities, and potential issues to both technical and non-technical stakeholders
Facilitate regular project meetings and status updates, ensuring effective communication and alignment
Resolve priority disputes and collaborate with stakeholders to ensure the team is working on the most critical tasks
Work closely with the cybersecurity team to track project progress, identify dependencies, and ensure alignment with security objectives
Provide project management support and expertise to the security team, fostering a collaborative and efficient working environment

What we offer

Medical, Dental, & Vision Insurance
401k Employer Matching
One Medical membership
Fertility Care & Family-Building Support
Professional Development Stipend
Unlimited PTO
Caregiving Benefit
Choice between a Mac or Linux equipment

Parttime

Board Certified Behavior Analyst

At EdTheory, our mission is to “Transform the lives and communities we serve, lo...

Location

United States , San Jose

Salary:

Not provided

EdTheory

Expiration Date

Until further notice

Requirements

Master’s Degree in Applied Behavior Analysis, Social Work, Counseling or closely related field Professional Certification
BCBA Certification
Comprehensive knowledge of behavioral disorders, therapeutic techniques and behavioral management planning
Valid California Driver’s License

What we offer

Travel Stipends for qualified travelers
Company Sponsored Benefits ( Medical, Dental, Vision, Group Life Insurance)
401(k) Retirement Plan with employer matching
Student Loan Pay Down Program, Grants and Scholarships
Relocation Bonus (extra bonus allocated for rural areas)
Travel Logistics Allowance (Temporary Lodging, License and Live Scan Travel, transport, etc.)
Wellness and Self-Care Stipend
EdCares Fund (Get paid to make a difference!)
EdPerks and Corporate Employee Discounts ( TAW, Gift card and subscription options across categories like ride-sharing, food delivery, cell phone allowance and pet care apps)
Yearly Summer Getaway Bonus

Fulltime

Epidemiology Analyst

Do you want an exciting position working with multiple teams to generate real wo...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Master's degree with 8 to 13 years of experience
Strong knowledge of observational research methodology
Excellent communication skills
Attention to detail
Ability to work across various therapeutic areas and regions
Experience in the design, execution, and analysis of observational research studies within Pharmaceutical or Public Health setting
Advanced expertise in medical codelist construction, maintenance, and quality assurance across standard clinical coding systems (e.g., ICD, MedDRA, SNOMED)
Experience in research to support drug development
Experience working with secondary data systems, including administrative claims, EMR, registries
Experience in observational research project planning and management

Job Responsibility

Contribute to global observational research activities for CfOR in support of drug development, registration, and commercialization across Amgen’s portfolio of products
Contribute to the implementation and conduct of observational studies to support the product lifecycle using real world databases and analytics platforms (e.g., Atlas, Aetion, and other internal/external RWD tools)
Develop, review, and maintain high-quality medical codelists for exposures, outcomes, covariates, and safety endpoints using standard coding systems (e.g., ICD, MedDRA, SNOMED, RxNorm), ensuring clinical validity and regulatory readiness
Partner with study team members to ensure codelists are fit-for-purpose, transparent, and reproducible across studies
Executes/manages descriptive epidemiologic studies to characterize the incidence/prevalence of disease in US, EU, Asia, and emerging market countries
Executes/manages research projects involving the analysis of multiple types of data including medical claims, electronic health records, and prospective observational cohort studies
Provides safety research support across the life cycle of Amgen products, supports the development of risk management plans, and executes pharmacovigilance studies
Conducts literature reviews and prepares research reports and scientific manuscripts
Stays abreast of the latest developments in the field of observational research and drug development
Promotes awareness, understanding, and use of observational research methods

New

Central Monitor - FSP

The Central Monitor (CM) plays a key role for Data Surveillance by overseeing an...

Location

Serbia

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

University degree in life science, business or operations
Fluent in both written and spoken English
≥ 5 years of recent pharmaceutical industry experience, with previous experience in clinical research, in a Pharmaceutical Industry or CROs
Strong clinical experience with excellent understanding of clinical trial development and risk management processes and the management of clinical trials
≥ 3 years comprehensive experience in monitoring (central, site), additional experience in clinical data analytics, data management activities or equivalent is preferable
Specific Central monitoring / monitoring experience (hands-on experience with KRIs review, centralized monitoring and quality tolerance limits -QTLs-) are strongly preferred
Knowledge of Risk-Based Quality Management (RBQM) and adaptive monitoring principles
Knowledge of overall clinical trial management process, understanding of the protocol, study associated risks and their significance, and the risk management process
Thorough understanding of the international aspects of drug development process, including expert knowledge of international standards (GCP/ICH)
Critical thinking and analytical skills to understand/analyze complex data and provide insight into risk signaling, trends, and outliers in data

Job Responsibility

Implement and execute centralized monitoring strategies to support clinical trial oversight
Conduct ongoing central monitoring analysis of clinical trial data to detect trends and signals
Work with Data Analysts team in reviewing CM technology outputs and performing an initial investigation of identified risks (e.g., atypical data patterns) to assess their scope and nature in preparation for review with study teams
As needed, provide input into the data domains required for central monitoring as per the monitoring strategy
Ensure adherence to risk-based monitoring plans, SOPs, and industry best practices
Perform data surveillance via the CM platform, identifying potential sites or trial risks in alignment with the IQRMP
Collaborate with Lead CM and study teams to refine and implement risk-based monitoring plans
Provide insights and recommendations to enhance trial efficiency and mitigate risks
Support root cause analysis for identified issues and suggest corrective actions
Generate and summarize findings within the CM platform and lead the communication of results to study teams and RSL

New

Central Monitor - FSP

The Central Monitor (CM) plays a key role for Data Surveillance by overseeing an...

Location

Romania

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

University degree in life science, business or operations
Fluent in both written and spoken English
≥ 5 years of recent pharmaceutical industry experience, with previous experience in clinical research, in a Pharmaceutical Industry or CROs
≥ 3 years comprehensive experience in monitoring (central, site), additional experience in clinical data analytics, data management activities or equivalent is preferable
Specific Central monitoring / monitoring experience (hands-on experience with KRIs review, centralized monitoring and quality tolerance limits -QTLs-) are strongly preferred
Knowledge of Risk-Based Quality Management (RBQM) and adaptive monitoring principles
Knowledge of overall clinical trial management process, understanding of the protocol, study associated risks and their significance, and the risk management process
Thorough understanding of the international aspects of drug development process, including expert knowledge of international standards (GCP/ICH)
Critical thinking and analytical skills to understand/analyze complex data and provide insight into risk signaling, trends, and outliers in data
Strong analytical and critical thinking skills with the ability to interpret complex clinical and operational data, recognize patterns, and identify potential risk signals or issues

Job Responsibility

Implement and execute centralized monitoring strategies to support clinical trial oversight
Conduct ongoing central monitoring analysis of clinical trial data to detect trends and signals
Work with Data Analysts team in reviewing CM technology outputs and performing an initial investigation of identified risks
As needed, provide input into the data domains required for central monitoring as per the monitoring strategy
Ensure adherence to risk-based monitoring plans, SOPs, and industry best practices
Perform data surveillance via the CM platform, identifying potential sites or trial risks in alignment with the IQRMP
Collaborate with Lead CM and study teams to refine and implement risk-based monitoring plans
Provide insights and recommendations to enhance trial efficiency and mitigate risks
Support root cause analysis for identified issues and suggest corrective actions
Generate and summarize findings within the CM platform and lead the communication of results to study teams and RSL

Scientist, LCMS PK Bioanalytical

An exciting opportunity is available for a Scientist to join the PK LCMS group i...

Location

United States , Andover

Salary:

79400.00 - 128500.00 USD / Year

Pfizer

Expiration Date

Until further notice

Requirements

MS with 4 to 6 years of relevant work experience, ideally mostly in industry (or BS/BA with 6 to 8 years of experience)
Expertise in development, characterization, and implementation of bioanalytical LCMS assays
Experience in the operation and troubleshooting of LCMS instrumentation and associated operating/data analysis software including Skyline, Analyst, Sciex OS and Xcalibur
Hands-on experience of biological sample preparation procedures for quantitative LCMS assays on biotherapeutics
Knowledge of writing scripts to set up methods for automated liquid handler system
Knowledge of protein biochemistry of therapeutic antibodies, fusion proteins or ADCs

Job Responsibility

Responsible for the development, qualification and implementation of PK/PD assays using mass spectrometry in support of discovery and preclinical projects
Works with group leads or other discovery and regulated bioanalytical team members and project team members to accomplish goals
Participates in technology development and implementation by exploring new workflows, including automation, high throughput sample preparation and instrumentation in protein quantitation, to expand the group’s PK LCMS bioanalytical capabilities
Participate in all phases of mass spectrometry laboratory operations including technology evaluations, the development of sample preparation and separation methods, data analysis, interpretation, reporting and follow up discussions with the project teams on utilizing the data in appropriate decision making
Ensure all tasks and responsibilities are carried out according to scientific and ethical standards e.g. responsible for electronic notebook record keeping
QC and peer review of data and reports

What we offer

401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution
paid vacation, holiday and personal days
paid caregiver/parental and medical leave
health benefits to include medical, prescription drug, dental and vision coverage
bonus target of 7.5% of the base salary
Relocation assistance may be available

Fulltime

Director of Research - Therapeutics

The Insights product is a new offering for Guidepoint's Institutional investment...

Location

United States , New York

Salary:

230000.00 - 250000.00 USD / Year

Modoras Accounting Syd

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Finance, Economics, Life Sciences, or a related field
advanced degrees (MBA, PhD) preferred
15+ years of investment related research experience on buyside or sell side covering Biotech/Pharma
12+ years of investment experience for Candidates who have MD or Ph.D degrees
Experience conducting therapeutics company research is required
Highly motivated and driven individual that demonstrated consistent outperformance
Proven track record of conducting and moderating expert interviews
Strong analytical skills with the ability to interpret complex information from various sources
Demonstrated experience in managing and developing teams, with effective mentoring capabilities
Excellent communication and interpersonal skills, with the ability to engage and influence stakeholders at all levels

Job Responsibility

Research Planning: Collaborate with the Global Head of Healthcare to design and implement primary research initiatives, focusing on key areas within Biotech/Pharma
Idea Generation: Generates ideas to generate content that are timely, topical, and aligned with the interests of US institutional investors
Expert Interviews: Lead and moderate interviews with physicians, researchers, and industry executives from Guidepoint’s extensive network of over 700,000 professionals, ensuring the extraction of valuable insights
Preparation and Analysis: Conduct thorough preparation for interviews by analyzing public company SEC filings, reviewing investor presentations, monitoring news releases, and assessing Wall Street research reports to ensure informed discussions
Team Management: Guide and mentor a team of junior analysts responsible for developing corporate content pertinent to the biotech and pharma sectors, fostering an environment of continuous learning and improvement
Client Engagement: Develop and implement client engagement plans that reflect the unique needs and pipeline of relevant clients, maximizing their utilization of our Insights content
Training and Development: Provide rigorous ongoing training for junior analysts on various industry topics, including market analysis, investment research methodologies, mergers & acquisitions, and leveraged buyouts to enhance their professional growth
Collaboration: Partner with the outreach team to highlight content that have actionable takeaways to clients

What we offer

15 PTO days, 10 legal holidays, and sick days
Comprehensive medical, dental, and vision plans
Will match up to 10% of employee contribution for 401(k), life insurance, paid time-off and parental leave plans
Commuter benefits and a corporate gym rate
Development opportunities through the LinkedIn Learning platform
Free snacks and beverages in the office
Friday happy hour and “Summer Fridays”
Year-round corporate athletic league
Casual work environment, team building, and other social events
Annual discretionary bonus based on performance

Fulltime

Equity Analyst

Guidepoint Insight is seeking an Equity Analyst to support the expansion of our ...

Location

China , Shanghai

Salary:

Not provided

Modoras Accounting Syd

Expiration Date

Until further notice

Requirements

Master or Advanced degrees in medicine, biological sciences or equivalent academic qualifications in medical professional degrees
Candidates with Ph.D. degree are preferred
3+ years of experience in financial services, investment research, covering Biotech / Pharma sector
3+ years of experience in pharmaceutical/biotech companies on competitive assessment, drug development, or business development will be considered as well
Demonstrated ability to understand and analyze pathophysiology of the disease, biological rationale of therapeutic targets, clinical data, drug labels and competitive dynamics
Strong understanding of institutional buy-side/sell-side research and investing workflows
Ability to work effectively in a fast-paced, entrepreneurial environment with a strong sense of ownership
Excellent organizational and time-management skills
Strong interpersonal skills with the ability to communicate effectively with professionals at all levels
Intellectual curiosity and a passion for learning about new industries and trends

Job Responsibility

Research Coverage: Monitor a coverage universe of Chinese public and private companies in biotech, pharma, medtech and services
Industry Analysis: Track key market and business drivers, including material news flows, earnings releases, investor presentations, clinical trials, medical conferences, product launches within your coverage companies and therapeutic indications
Report Creation: Collect and organize clinical trial information and results, analyze the mechanisms of action (MOA) of drug candidates, investigate clinical paradigms for disease treatment in China, and prepare reports
Content Development: Create and moderate teleconferences featuring experts from Guidepoint’s network summarized in high-quality, detailed transcripts
Content Editing: Ensure high-quality content creation and editing of teleconference transcripts. Summarize, edit, and vet key discussion points of these teleconferences
Reporting: Collaborate with the Director of Research to drive the growth of Guidepoint’s content library, scaling research coverage across multiple industries
Strategic Collaboration: Work closely with cross-functional teams, to align research initiatives with business objectives and market demands
Compliance & Integrity: Uphold Guidepoint’s compliance policies by ensuring that expert profiles and teleconference content adhere to company protocols

What we offer

Competitive compensation
Entrepreneurial environment, autonomy, and fast decisions
International exposure to the global Guidepoint service teams
Casual work environment
Summer and winter team events

Analyst - Therapeutics

Modoras Accounting Syd

Location:
India , Mumbai

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
February 18, 2026

Looking for more opportunities? Search for other job offers that match your skills and interests.

Similar Jobs for Analyst - Therapeutics

Junior Cybersecurity Analyst

Board Certified Behavior Analyst

Epidemiology Analyst

Central Monitor - FSP

Central Monitor - FSP

Scientist, LCMS PK Bioanalytical

Director of Research - Therapeutics

Equity Analyst

Analyst - Therapeutics

Modoras Accounting Syd

Location:India , Mumbai

Category:Research and Development

Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:February 18, 2026

Looking for more opportunities? Search for other job offers that match your skills and interests.

Similar Jobs for Analyst - Therapeutics

Junior Cybersecurity Analyst

Board Certified Behavior Analyst

Epidemiology Analyst

Central Monitor - FSP

Central Monitor - FSP

Scientist, LCMS PK Bioanalytical

Director of Research - Therapeutics

Equity Analyst

Location:
India , Mumbai

Category:
Research and Development

Contract Type:
Not provided

Job Posted:
February 18, 2026