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Senior Medical Writer, Promotional Review

54-1759539 Evidera, Inc.

LocationUnited States
SenioritySenior
Company54-1759539 Evidera, Inc.
Verified recentlyOct 15
Compensation

$115k-$125k

Salary details are shown when available from the source listing. Sign in before applying so the role can be reviewed against your resume, salary goals, seniority, timezone, and location eligibility.

Requirements and working style

Decision details from the source listing

Experience

5+ years stated

Education

Bachelor's degree in a scientific discipline or equivalent relevant formal academic or vocational qualification, Advanced degree preferred

Schedule

fixed

Benefits stated
Medical, dental, and vision plansHealth incentive programsEmployee assistance and family support programsCommuter benefitsTuition reimbursementAt least 120 hours of paid time off10 paid holidays annuallyPaid parental leaveAccident and life insuranceShort- and long-term disability401(k) retirement savings planEmployee Stock Purchase PlanPotential variable annual bonus

These fields are normalized from the employer's text. Confirm details on the employer site before applying.

WFH.team analysis

What this posting tells you

Senior Medical Writer role focused on clinical and scientific documents, including study reports, protocols, and regulatory materials. The listing identifies the position as fully remote in the United States, while also describing office working conditions and occasional domestic and international travel. Requires a bachelor's degree or equivalent and typically 5+ years of relevant experience. California salary range is $115,000–$125,000.

Role lane

Data, Education, Healthcare admin, Product, Security, Software, Customer support, Writing and content

Where you can work

United States

Working hours

Timezone overlap is not stated.

Arrangement

Senior · contract · full_time

Required signals
Medical and scientific writingData interpretationEditing and proofreadingClinical study reports and protocolsProject managementRegulatory and document development guidelinesTherapeutic area expertiseCommunication and presentation
Preferred signals
Pharmaceutical or CRO industry experienceMedical writing qualifications (AMWA, EMWA, or RAC)Experience with preclinical, therapeutic, regulatory submissions, or communications
Confirm before applying
  • Required timezone overlap is not stated
Market context

Data hiring on WFH.team

9,338active related roles
3,770new in the latest period
355.6jobs per 100 candidates
$167kmedian of comparable listed ranges

This role's listed pay is below the median among 200 comparable roles shown here. Category counts come from WFH.team's latest published remote job market snapshot.

Explore the remote job market
Skills and signals
Medical and scientific writingData interpretationEditing and proofreadingClinical study reports and protocolsProject managementRegulatory and document development guidelinesTherapeutic area expertiseCommunication and presentationPharmaceutical or CRO industry experienceMedical writing qualifications (AMWA, EMWA, or RAC)Experience with preclinical, therapeutic, regulatory submissions, or communicationsFully remote; listed for the United States, with California and Carlsbad also mentioned
Job description

Senior Medical Writer, Promotional Review at 54-1759539 Evidera, Inc.

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Senior Medical Writer - Make an Impact at the Forefront of Innovation

The Senior Medical Writer provides high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients and demonstrates subject matter and therapeutic area expertise. The Senior Medical Writer may assist program manager. The role involves collaborating with internal and external clients, supporting and enabling effective and efficient communication that results in operational excellence.

What you'll do

  • Serve as primary author who writes and provides input on routine documents such as clinical study reports and study protocols, and summarizes data from clinical studies.
  • May research, write or edit complex clinical and scientific and program level documents, including IBs, INDs, and MAAs.
  • Review routine documents prepared by junior team members. May provide training and mentorship for junior writers and program managers on document preparation, the use of software for document development, document types, regulatory requirements, and therapeutic area knowledge.
  • Ensure compliance with quality processes and requirements for assigned documents. Provide input on and independently develops best practices, methods and techniques for achieving optimal results, including various client specific processes.
  • May assist in program management activities. Identify and resolve out-of-scope activities. Duties could include developing timelines, budgets, forecasts and contract modifications.
  • Represent the department at project launch meetings, review meetings, and project team meetings.

Education & Experience Requirements

  • Bachelor's degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification; Advanced degree preferred
  • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years).
  • Experience working in the pharmaceutical/CRO industry preferred
  • Additional qualifications in medical writing (AMWA; EMWA; RAC) advantageous

Years of experience refers to typical years of related experience needed to gain the required knowledge, skills, and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection decisions.

Knowledge, Skills, Abilities

  • Excellent data interpretation and medical writing skills, including grammatical, editorial, and proofreading skills
  • Strong project management skills
  • Excellent interpersonal skills including problem solving
  • Strong negotiation skills
  • Excellent oral and written communication skills with strong presentation skills
  • Significant knowledge of global, regional, national and other document development guidelines
  • In-depth knowledge in a specialty area such as preclinical, therapeutic, regulatory submissions, communications, etc.
  • Great judgment and decision-making skills
  • Excellent computer skills and skilled with client templates; Good knowledge of document management systems and other relevant applications (e.g. Excel, Outlook)

Working Conditions and Environment

  • Work is performed in an office environment.
  • Exposure to electrical office equipment.
  • Occasional drives to site locations with occasional travel both domestic and international.
  • Long, varied hours required occasionally.

Why Join Us?

When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthroughs.

Compensation and Benefits

The salary range estimated for this position based in California is $115,000.00–$125,000.00.

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

  • A choice of national medical and dental plans, and a national vision plan, including health incentive programs
  • Employee assistance and family support programs, including commuter benefits and tuition reimbursement
  • At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
  • Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
  • Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

Company context

Working remotely at 54-1759539 Evidera, Inc.

54-1759539 Evidera, Inc. is hiring for 2 active remote roles, with remote-friendly openings, application links, and job details refreshed from the public remote job inventory.

Remote policy

Remote hiring signal is inferred from active confirmed-remote job listings.

Research 54-1759539 Evidera, Inc.