Contract - Clinical Scientist
Contract - Clinical Scientist
Posted on :
24-01-2025
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1 Vacancy
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Monthly Salary
Not Disclosed
Salary Not Disclosed
Vacancy
1 Vacancy
Posted on :
24-01-2025
Job Description
Job Title: Contract Clinical Scientist
Job Location: United States
Job Location Type: Remote
Job Contract Type: Contract
Job Seniority Level: MidSenior level
Cytokinetics is a latestage specialty cardiovascular biopharmaceutical company focused on discovering developing and commercializing firstinclass muscle activators and nextinclass muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.
The Clinical Scientist will play a critical role in the analysis of research study data both in early and late phases of development. This role will collaborate closely with the medical leads for clinical studies clinical pharmacology and drug safety teams. The clinical Scientist will report directly to the Chief Medical Officer and will be instrumental in interpreting complex data sets creating highimpact scientific content and representing Cytokinetics at medical conferences and in peerreviewed publications.
Key Responsibilities:
How to Apply:
Interested candidates should submit a resume and cover letter outlining their qualifications and interest in the role to .
Our employees come from different backgrounds and we celebrate those differences. We are looking for the best candidates for our open roles but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team we would love to hear from you.
Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.
Our passion is anchored in robust scientific thinking grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity ethics doing the right thing and being our best selves.
Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers
Recently there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process.
Here are some ways to check for authenticity:
Cytokinetics is an Equal Opportunity Employer
The Clinical Scientist will play a critical role in the analysis of research study data both in early and late phases of development. This role will collaborate closely with the medical leads for clinical studies clinical pharmacology and drug safety teams. The clinical Scientist will report directly to the Chief Medical Officer and will be instrumental in interpreting complex data sets creating highimpact scientific content and representing Cytokinetics at medical conferences and in peerreviewed publications.
Key Responsibilities:
- Collaborate with medical leads in the planning of early and latephase clinical research studies.
- Work closely with clinical pharmacology and drug safety teams to integrate pharmacokinetic and safety data into overall clinical study designs.
- Provide outputs that may be incorporated into documents such as investigator brochures clinical study reports and other regulatory documents.
- Conduct data reviews of clinical data sets and participate in statistical analyses in collaboration with biostatisticians.
- Develop data visualization strategies to effectively communicate clinical trial data and outcomes.
- Prepare scientific presentations for internal and external audiences including scientific conferences advisory boards and regulatory meetings.
- Contribute to the preparation and submission of manuscripts for publication in peerreviewed journals ensuring adherence to Good Publication Practices (GPP).
- Support the development of clinical study documents including study protocols and patientfacing materials.
- Maintain uptodate knowledge of relevant scientific literature therapeutic area trends and regulatory requirements impacting clinical trials and drug development.
- Advanced degree (MD PhD PharmD; MS with additional direct experience) in a life sciences or healthrelated field strongly preferred.
- 3 years of experience in clinical research preferably within the biopharmaceutical or biotechnology industry.
- Strong understanding of biostatistics and experience in interpreting clinical data.
- Proficiency in medical writing and developing highquality scientific documents.
- Familiarity with Good Publication Practices (GPP) and experience in ensuring compliance with GPP guidelines in scientific writing and publication.
- Experience with data visualization tools (e.g. GraphPad Prism Tableau R) and presentation software (e.g. PowerPoint).
- Proven ability to create and generate scientific presentations for consumption by a diverse audiences.
- Familiarity with clinical trial design execution and regulatory requirements (e.g. FDA EMA).
- Excellent organizational interpersonal and communication skills.
- Ability to work collaboratively in a multidisciplinary team environment.
- Strong attention to detail and ability to manage multiple tasks simultaneously.
- Experience in muscle biology cardiology neurology or related therapeutic areas.
- Knowledge of pharmacokinetics and pharmacodynamics.
- Previous experience presenting at scientific conferences or contributing to peerreviewed publications.
How to Apply:
Interested candidates should submit a resume and cover letter outlining their qualifications and interest in the role to .
Our employees come from different backgrounds and we celebrate those differences. We are looking for the best candidates for our open roles but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team we would love to hear from you.
Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.
Our passion is anchored in robust scientific thinking grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity ethics doing the right thing and being our best selves.
Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers
Recently there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process.
Here are some ways to check for authenticity:
- We do not conduct job interviews through nonstandard text messaging applications
- We will never request personal information such as banking details until after an official offer has been accepted and verified
- We will never request that you purchase equipment or other items when interviewing or hiring
- If you are unsure about the authenticity of an offer or if you receive any suspicious communication please contact us directly at
Cytokinetics is an Equal Opportunity Employer
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Employment Type
Full Time
Key Skills
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