Clinical Specialist - General Medicine
USA - Pennsylvania - North Wales (Upper Gwynedd)
Job Description
Job Summary
The Clinical Specialist position is a combined position of clinical scientist and study management duties supporting one or more clinical trials. Under the oversight of a clinical scientist, study manager, or program lead, the Clinical Specialist may be responsible for but not limited to:
Job Responsibilities
- Maintain clinical trial files (including eTMF), project processes, tracking systems, and other utilized study or departmental systems
- Generating and reviewing medical monitoring reports
- Creating and maintaining project schedules
- Distributing, reconciling, and archiving clinical documents
- Tracking and reconciling labs/samples
- May interact with internal and external stakeholders (e.g., study sites, committees) in support of clinical trial objectives
Core Skills
- Pharmaceutical, research, medical, and/or clinical drug development knowledge/experience
- Strong communication, writing, and presentation skills
- Effective time management and organizational skills
- Ability to effectively work in a team environment and independently
- Proficient knowledge in Microsoft office or similar (Excel, PowerPoint, Word, Outlook, etc.)
- Preferred: knowledge of GCP, project management, process improvement, data analytics
Education/Experience
- Bachelor's Degree +1 years of pharmaceutical, clinical drug development, project management, and/or medical field experience OR Master's Degree
- Degree in life sciences, preferred.
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Current Employees apply HERE
Current Contingent Workers apply HERE
US and Puerto Rico Residents Only:
Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.
We are an Equal Opportunity Employer, committed to fostering an inclusive and diverse workplace. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status, or other applicable legally protected characteristics. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:
Pay Transparency Nondiscrimination
We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.
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U.S. Hybrid Work Model
Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as “remote”.
The Company is required to provide a reasonable estimate of the salary range for this job in certain states and cities within the United States. Final determinations with respect to salary will take into account a number of factors, which may include, but not be limited to the primary work location and the chosen candidate’s relevant skills, experience, and education.
Expected US salary range:
$68,400.00 - $107,700.00Available benefits include bonus eligibility, long term incentive if applicable, health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and sick days. A summary of benefits is listed here.
San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance
Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
RegularRelocation:
No relocationVISA Sponsorship:
NoTravel Requirements:
10%Flexible Work Arrangements:
HybridShift:
Not IndicatedValid Driving License:
NoHazardous Material(s):
n/aJob Posting End Date:
11/25/2024*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
ApplyJob Profile
Hybrid Hybrid work Hybrid work model In-person attendance required for certain positions On-site Puerto Rico residents only US and Puerto Rico residents only
Benefits/PerksAccommodation during hiring process Bonus eligibility Diverse workplace Equal opportunity employer Flexible work Flexible work arrangements Health Care Hybrid work Hybrid work model Inclusion Inclusive environment Inclusive workplace Insurance Paid holidays Retirement benefits Sick Days Team environment Vacation
Tasks- Communication
- Compliance
- Create and maintain project schedules
- Distribute and archive clinical documents
- Generate and review medical monitoring reports
- Innovation
- Interact with stakeholders
- Maintain clinical trial files
- Medical monitoring
- Presentation
- Process Improvement
- Project management
- Track and reconcile labs/samples
Analytics Clinical Clinical drug development Clinical trials Communication Compliance Data Data & Analytics Development Drug Development Education ETMF Excel GCP Inclusion Innovation Life sciences Management Manufacturing Medical Medical field Medical Monitoring Medicine Microsoft Office Monitoring Organization Organizational Outlook Pharmaceutical PowerPoint Presentation Process Improvement Project Management Research Teamwork Time Management Word Writing
Experience1 years
EducationAS Bachelor Bachelor's Bachelor's degree Business Data Analytics Health Care Life Sciences Management Master Master's Master's degree
Certifications TimezonesAmerica/Anchorage America/Chicago America/Denver America/Los_Angeles America/New_York Europe/London Pacific/Honolulu UTC+0 UTC-10 UTC-5 UTC-6 UTC-7 UTC-8 UTC-9