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Remote Muscle Biology Jobs (NOW HIRING)

Cytokinetics

Contract Clinical Systems Specialist

$75 - $86/hr

... muscle biology, and advancing a pipeline of potential new medicines for patients suffering from ... Good organization skills, ability to manage multiple tasks #LI-REMOTE Pay Range: In the U.S., the ...

Arvinas

ARV-027, targeting the polyglutamine-expanded androgen receptor, or polyQ-AR, in skeletal muscle ... Partner with discovery and biology leadership and provide clinical input and guidance to develop ...

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Remote Muscle Biology information

What is the difference between Remote Muscle Biology vs Remote Exercise Science?

AspectRemote Muscle BiologyRemote Exercise Science
Required CredentialsBachelor's in Biology, Anatomy, or related field; certifications in anatomy or physiologyBachelor's in Exercise Science, Kinesiology, or related; certifications like ACSM or NSCA
Work EnvironmentResearch, analysis, and educational content creationProgram design, client consultation, and fitness assessment
Industry UsageAcademic research, health education, biotechPersonal training, sports performance, wellness programs
Search & Comparison IntentUnderstanding biological aspects of muscles remotelyDesigning exercise programs or fitness consulting remotely

Remote Muscle Biology focuses on understanding muscle structure and function through research and education, often requiring biology or anatomy credentials. Remote Exercise Science emphasizes designing fitness programs and consulting clients remotely, requiring exercise science certifications. Both roles are in health and fitness industries but serve different purposes and skill sets.

What are the key skills and qualifications needed to thrive as a Remote Muscle Biologist, and why are they important?

To thrive as a Remote Muscle Biologist, you need a strong background in cell biology, physiology, and molecular techniques, typically supported by an advanced degree in biology or a related field. Familiarity with bioinformatics tools, laboratory information management systems (LIMS), and data analysis software is often required. Excellent written communication, self-motivation, and collaboration skills are crucial for effective remote teamwork and reporting. These skills enable accurate research, efficient data sharing, and meaningful contributions to scientific advancements despite working remotely.

What is a Remote Muscle Biologist?

A Remote Muscle Biologist is a scientific professional who studies the structure, function, and diseases of muscles, but conducts their work remotely using digital tools and data analysis platforms. They may analyze data, design experiments, collaborate with teams, and write research papers from a remote location rather than a traditional laboratory. This role often requires strong skills in bioinformatics, virtual communication, and independent research. Remote Muscle Biologists typically work for universities, biotech companies, or research organizations involved in muscle biology and related fields.

How do remote Muscle Biology professionals typically collaborate with laboratory-based teams?

Remote Muscle Biology professionals often collaborate closely with lab-based teams through regular virtual meetings, data sharing platforms, and project management tools. While they might not be physically present in the lab, they contribute to experimental design, data analysis, literature reviews, and manuscript preparation. Effective communication is crucial, as remote team members may guide lab experiments, interpret results, and provide scientific insight from a distance. Building strong relationships with onsite colleagues and maintaining clear documentation are key to overcoming the challenges of remote scientific collaboration.
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Remote Muscle Biology jobs near you
Senior Clinical Research Associate - Cardiovascular (EDG-2026033)

Senior Clinical Research Associate - Cardiovascular (EDG-2026033)

Edgewise Therapeutics

MH • On-site, Remote

$90 - $140/hr

Full-time

Medical, Retirement, PTO

Posted 8 days ago

Job description

Senior Clinical Research Associate - Cardiovascular
About Edgewise Therapeutics:
At Edgewise, we are on a mission to discover new medicines that improve the lives of patients facing serious muscle disease. Our intimate knowledge of muscle biology and biophysics along with our ability to identify and design muscle specific precision small molecules have enabled us to rapidly advance our skeletal muscle and cardiac muscle product candidates into the clinic while also building a robust pre-clinical pipeline. With this focus on therapeutics designed to protect and improve muscle health, our goal is to dramatically enhance the lives of people living with progressive muscle disorders.
We have assembled an experienced and highly motivated leadership team with a strong track record in the biotechnology and pharmaceutical industry to build the leading, global muscle disease biopharmaceutical company. Come join us make a significant difference in the lives of patients!
About the Position:
Edgewise is headquartered in Boulder, Colorado; this is a position for a growing Colorado-based Clinical Development team. The assigned clinical trials will be highly complex and high risk, e.g. multiple indications, data monitoring committees, interim analyses, adaptive design, requiring the coordination of multiple vendors, or other special assessments. Candidates may be asked to provide support to the Edgewise clinical study lead for more than one study or across programs.
Key Responsibilities:
  • Lead site start-up activities (e.g. oversight of CRO start-up activities, accountable for essential document package review, site initiation slide deck, vendor training, participate in remote/or on-site initiation visits) and contribute to feasibility, as required.
  • Collaborate with contracts team to lead review and negotiation of site and vendor budgets/contracts.
  • Contribute to the development and review of study, patient and site facing documents (e.g. protocols, ICFs and study plans).
  • Oversee Edgewise contract CRA and/or CRO monitoring activities (e.g. visit schedules, monitoring visit reviews, monitoring plan review). May include on-site co-monitoring with CRO CRA, ensuring compliance with protocol and regulatory requirements. Provide additional clinical monitoring training support to CRO personnel, as needed. Attend CRO monitoring meetings. May include assigned monitoring responsibilities for sites.
  • Review and oversee site KPIs, protocol deviations and metrics to identify trends and maintain data quality. Escalate site level risks or non-compliance, and in collaboration with Quality Assurance, review Site Corrective and Action Plans (SCAPAs), Corrective and Action Plans (CAPAs) and Site Audits.
  • Support the Edgewise clinical study lead in managing progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment and other tasks as assigned.
  • Proactively review electronic data capture (EDC) for completion and to identify issues and generate queries. Identify and monitor risks and decisions at the study level and implementation of mitigation strategies. Identify potential operational challenges, and in collaboration with senior team members, provide guidance and solutions to ensure study execution remains on track.
  • Contribute to drafting Standard Operating Procedures (SOPs) and adhere to Clinical Operations processes and SOPs to ensure studies are "inspection ready" at all times; may be involved in regulatory inspections by preparing for and attending the inspections.
  • Responsible for the oversight of assigned vendors.
  • Collaborate with internal teams (e.g. Clinical Operations, Regulatory Affairs, Data Management, Medical Monitoring, CMC, etc.) to ensure seamless trial execution and provide regular study updates to the appropriate internal stakeholders.
  • May be accountable for reviewing site or vendor invoicing and financial management in accordance with the clinical trial agreement / scope of work.
  • Support TMF activities as required (e.g. review of TMF index, document provision, etc.).
  • Support onboarding and mentoring of new department members.

Required Education, Experience, Skills:
  • At least 4+ years of relevant clinical operations experience and a BS or BA (Life Sciences)
  • Minimum 4 years of independent on-site monitoring experience (across all visit types and inclusive of remote monitoring), with at least 3 years cardiac study experience in a pharmaceutical sponsor environment preferred (global pharma or biotech preferred).
  • Excellent attention to detail, verbal, written, interpersonal and presentation skills are required
  • Must be familiar with routine medical/scientific terminology.
  • Proficiency with MS Office required (inclusive of PPT), Smart Sheet proficiency desirable
  • Knowledge of FDA, ICH Guidelines, and GCPs governing the conduct of clinical trials is required
  • Must be able to participate in departmental or interdepartmental strategic initiatives under general supervision
  • Highly productive, engaged and accountable
  • Team-player desiring to work in a fast-moving, dynamic start-up environment

This is a full-time position (40 hours/week), hybrid, Colorado based preferred. 20-50% travel.
Salary range: $90,000 - $140,000, title and salary commensurate with experience
Our Benefits: We are proud to offer health benefits, a discretionary bonus plan, stock option grants. a stock purchase plan, a 401(k) with match and paid time off to our team members as part of their compensation plan.
There is no deadline because the employer accepts applications on an ongoing basis.
Edgewise does not accept resumes from recruitment agencies for this position. Please do not send resumes to Edgewise employees or the company location. Edgewise is not responsible for any fees related to unsolicited resumes.

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