Stryker
Senior Clinical Project Manager (Remote)
Senior Clinical Project Manager (Remote) assists in global clinical evidence planning, clinical study design, and communication with assigned business units. The position contributes to the Clinical Research team activities for designated projects and ensures patient safety, quality and integrity of data, compliance with relevant SOPs and regulatory requirements, and completes studies on‑time and on‑budget.
What You Will Do
Works closely with key internal (Marketing, R&D, Market Access, Product Development) and external stakeholders (surgeon researchers) to develop global clinical evidence generation plans to support the various needs of the business (e.g., regulatory filings, supporting claims).
Maintains relationships with Key Opinion Leaders in support of Clinical Affairs activities.
Manage assigned Investigator Initiated Study proposals, reviews, and conduct.
Supports the development of publication plans and their execution in combination with relevant internal and external resources.
Supports and helps manage creation of publication summaries and dissemination of this information.
Supports Clinical Research team, sometimes serving as the Clinical representative, interactions with regulatory authorities, notified bodies and during audits.
Supports, sometimes serves as the point person, communicating project status updates, resource needs, and other information for assigned business units and product lines.
Supports study design processes, including protocol development, while working closely with the Clinical Operations and Clinical Data Sciences teams.
What You Need
Bachelor’s degree required; in a health sciences; preference for degrees in biological sciences, engineering, or related medical/scientific field preferred.
6+ years’ experience directly supporting clinical device research or similar experience in a medical device scientific area.
Understanding of industry clinical research regulations and best practices (e.g., ISO 14155, ICH GCP).
Preferred
Excellent interpersonal skills and the ability to work well independently as well as with co‑workers, peers, supervisors, and external customers.
High attention to detail and accuracy.
$105,500.00 - $173,900.00 USD Annual salary plus bonus eligible + benefits. Individual pay is based on skills, experience, and other relevant factors.
This role will be posted for a minimum of 3 days.
Benefits Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness insurance, accident insurance, hospital indemnity insurance, personalized healthcare support, wellbeing program and tobacco cessation program. Financial benefits include: Health Savings Account (HSA), Flexible Spending Accounts (FSAs), 401(k) plan, Employee Stock Purchase Plan (ESPP), basic life and AD&D insurance, and short-term disability insurance.
Seniority Level
Mid‑Senior level
Employment Type
Full‑time
Job Function
Project Management and Information Technology
Industries: Appliances, Electrical, and Electronics Manufacturing; Industrial Machinery Manufacturing; Medical Equipment Manufacturing
Location: New York, NY (remote position) – applicants located worldwide may apply.
#J-18808-Ljbffr
What You Will Do
Works closely with key internal (Marketing, R&D, Market Access, Product Development) and external stakeholders (surgeon researchers) to develop global clinical evidence generation plans to support the various needs of the business (e.g., regulatory filings, supporting claims).
Maintains relationships with Key Opinion Leaders in support of Clinical Affairs activities.
Manage assigned Investigator Initiated Study proposals, reviews, and conduct.
Supports the development of publication plans and their execution in combination with relevant internal and external resources.
Supports and helps manage creation of publication summaries and dissemination of this information.
Supports Clinical Research team, sometimes serving as the Clinical representative, interactions with regulatory authorities, notified bodies and during audits.
Supports, sometimes serves as the point person, communicating project status updates, resource needs, and other information for assigned business units and product lines.
Supports study design processes, including protocol development, while working closely with the Clinical Operations and Clinical Data Sciences teams.
What You Need
Bachelor’s degree required; in a health sciences; preference for degrees in biological sciences, engineering, or related medical/scientific field preferred.
6+ years’ experience directly supporting clinical device research or similar experience in a medical device scientific area.
Understanding of industry clinical research regulations and best practices (e.g., ISO 14155, ICH GCP).
Preferred
Excellent interpersonal skills and the ability to work well independently as well as with co‑workers, peers, supervisors, and external customers.
High attention to detail and accuracy.
$105,500.00 - $173,900.00 USD Annual salary plus bonus eligible + benefits. Individual pay is based on skills, experience, and other relevant factors.
This role will be posted for a minimum of 3 days.
Benefits Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness insurance, accident insurance, hospital indemnity insurance, personalized healthcare support, wellbeing program and tobacco cessation program. Financial benefits include: Health Savings Account (HSA), Flexible Spending Accounts (FSAs), 401(k) plan, Employee Stock Purchase Plan (ESPP), basic life and AD&D insurance, and short-term disability insurance.
Seniority Level
Mid‑Senior level
Employment Type
Full‑time
Job Function
Project Management and Information Technology
Industries: Appliances, Electrical, and Electronics Manufacturing; Industrial Machinery Manufacturing; Medical Equipment Manufacturing
Location: New York, NY (remote position) – applicants located worldwide may apply.
#J-18808-Ljbffr